NZ548497A - Fungal lipolytic enzymes - Google Patents

Abstract

Disclosed is a fungal lipolytic enzyme wherein the enzyme comprises an amino acid sequence as shown in SEQ ID No. 1 or SEQ ID No. 2 or SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity to anyone of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 4 or SEQ ID No. 6. The enzymes disclosed have a higher ratio of activity on polar lipids compared with triglycerides and can be used to prepare lyso-phospholipids and food products.

Description

548497 1 FUNGAL LIPOLYTIC ENZYMES FIELD OF THE INVENTION The present invention relates to novel fungal lipolytic enzymes and to one or more 5 polynucleotides encoding one or more novel fungal lipolytic enzymes. The invention also relates to methods of producing fungal lipolytic enzymes, and uses thereof. The present invention further relates to the preparation of an improved foodstuff, in particular to the preparation of improved bakery products. Specifically, the invention provides novel fungal lipolytic enzymes, which enzymes are capable of conferring 10 improved characteristics to food products, including bakery products.

TECHNICAL BACKGROUND The beneficial use of lipolytic enzymes (E.C. 3.1.1.x) in food and/or feed industrial 15 applications has been known for many years.

For instance, in EP 0 585 988 it is claimed that lipase addition to dough resulted in an improvement in the antistaling effect. It is suggested that a lipase obtained from Rhizopus arrhizus when added to dough can improve the quality of the resultant bread 20 when used in combination with shortening/fat W094/04035 teaches that an improved bread softness can be obtained by adding a lipase to dough without the addition of any additional fat/oil to the dough. Castello, P. ESEGP 89-10 Dec. 1999 Helsinki, shows that exogenous lipases can modify bread volume.

The substrate for lipases in wheat flour is 1.5-3% endogenous wheat lipids, which are a complex mixture of polar and non-polar lipids. The polar lipids can be divided into glycolipids and phospholipids. These lipids are built up of glycerol esterified with two fatty acids and a polar group. The polar group contributes to surface activity of these lipids. Enzymatic cleavage of one of the fatty acids in these lipids leads to lipids with 30 a much higher surface activity. It is well known that emulsifiers, such as DATEM, with high surface activity are very functional when added to dough. intellectual property office of n.z. 1 6 SEP 2009 fl P n F I V lr D 548497 2 Lipolytic enzymes hydrolyse one or more of the fatty acids from lipids present in the food which can result in the formation of powerful emulsifier molecules within the foodstuff which provide commercially valuable functionality. The molecules which 5 contribute the most significant emulsifier characteristics are the partial hydrolysis products, such as lyso-phospholipids, lyso-glycolipids and mono-glyceride molecules. The polar lipid hydrolysis products, namely lyso-phospholipids and lyso-glycolipids, are particularly advantageous. In bread making, such in situ derived emulsifiers can give equivalent functionality as added emulsifiers, such as DATEM.

However, the activity of lipolytic enzymes has also been found to result in accumulation of free fatty acids, which can lead to detrimental functionality in the foodstuff. This inherent activity of lipolytic enzymes limits their functionality.

The negative effect on bread volume is often explained by overdosing. Overdosing can lead to a decrease in gluten elasticity which results in a dough which is too stiff and thus results in reduced volumes. In addition, or alternatively, such lipases can degrade shortening, oil or milk fat added to the dough, resulting in off-flavour in the dough and baked product. Overdosing and off-flavour have been attributed to the 20 accumulation of free fatty acids in the dough, particularly short chain fatty acids.

The presence of high levels of free fatty acids (FFA) in raw materials or food products is generally recognised as a quality defect and food processors and customers will usually include a maximum FFA level in the food specifications. The resulting effects 25 of excess FFA levels can be in organoleptic and/or functional defects.

In EP 1 193 314, the inventors discovered that the use of lipolytic enzymes active on glycolipids was particularly beneficial in applications in bread making, as the partial hydrolysis products the lyso-glycolipids were found to have very high emulsifier 30 functionality, apparently resulting in a higher proportion of positive emulsifier functionality compared to the detrimental accumulation of free fatty acids. However, 548497 3 the enzymes were also found to have significant non-selective activity on triglycerides which resulted in unnecessarily high free fatty acid.

This problem of high triglyceride activity was addressed in WO 02/094123, where the 5 inventors discovered that by selecting lipolytic enzymes which were active on the polar lipids (glycolipids and phospholipids) in a dough, but substantially not active on triglycerides or 1-mono-glycerides, an improved functionality could be achieved.

A commercially preferred source of lipase enzymes is filamentous fungi, such as 10 Aspergillus spp. and Fusarium spp. Lipases isolated from filamentous fungi have been found to have industrially applicable characteristics and also have been found to be routine to express in heterologous production systems, such as in Aspergillus oiyzae, Fusarium and yeast.

A lipase from Fusarium. oxysporum was identified in EP 0 130 064, and the application of F. oxysporum lipases in food applications has been suggested in Hoshino etal. (1992) Biosci. Biotech. Biochem 56: 660-664.

EP0 869 167 describes the cloning and expression of a Fusarium oxysporum lipase and 20 its use in baking. The enzyme is described as having phospholipase activity. This enzyme is now sold by Novozymes A/S (Denmark) as Lipopan F™.

WO 02/00852 discloses five lipase enzymes and their encoding polynucleotides, isolated from F. venenatum, F. sulphurewn, A. berkeleyanum, F. culmorwn and F. 25 solani, All five enzymes are described as having triacylglycerol hydrolysing activity, phospholipase and galactolipase activity. Three of the enzymes have equivalent activity to the F.oxysporum enzyme taught in EP 0 869 167: F. venenatum, F. sulphurewn, F. culmorum.

Therefore, it is apparent that some Fusarium lipases, including Lipopan F™ have been found to have side activity on polar lipids, including phospholipids and glycolipids. Although described as a phospholipase in EP 0 869 167, the lipase from Fusarium 548497 4 oxysporum lias high lipase activity. The enzyme also has glycolipase activity. However, despite the significant activity on polar lipids, the functionality achieved by use of the enzyme is limited due to the high lipase (i.e. triglyceride) activity.

Nagao et al (J. Biochem 116 (1994) 536-540) describes a lipase from F. heterosporum; which enzyme predominantly functions as a lipase (E.C. 3.1.1.3) to hydrolyse triglycerides. This is very different from the enzymes according to the present invention.

Lipolytic enzyme variants, with specific amino acid substitutions and fusions, have been produced some of which have an enhanced activity on the polar lipids compared to fee wild-type parent enzymes. W001/39602 describes such a variant, referred to as SP979, which is a fusion of the Thermomyces lanuginosus lipase, and the Fusarium oxysporum lipase described in EP 0 869 167. This variant has been found to have a 15 significantly high ratio of activity on phospholipids and glycolipids compared to triglycerides.

However, prior to the present invention, natural fungal lipolytic enzymes, particularly from Fusarium spp., having a high ratio of activity on polar lipids compared with 20 triglycerides had not been taught.

SUMMARY OF THE INVENTION In a first aspect the present invention relates to a fungal lipolytic enzyme wherein the 25 enzyme comprises an amino acid sequence as shown in SEQ ID No. 1 or SEQ ID No. 2 or SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity to any one of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 4 or SEQ ID No. 6.

I intellectual property office OF n z. 1 6 SEP 2009 RECEIVED i 548497 In a second aspect the present invention relates to a nucleic acid encoding a novel fungal lipolytic enzyme of the first aspect of the invention.

In a third aspect the present invention relates to a method of preparing a foodstuff, preferably an egg-based foodstuff, the method comprising adding a fungal lipolytic enzyme of the first aspect of the invention or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to one or more ingredients of the foodstuff.

The present invention relates to a method of preparing a dough, the method comprising adding a fungal lipolytic enzyme of the first aspect of the invention or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to one or more ingredients of the dough and mixing to form a dough.

Another broad aspect of the present invention relates to a method of preparing a baked product from a dough, the method comprising adding a fungal lipolytic enzyme of the first aspect of the invention or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to the dough.

There is also provided a method of preparing a fungal lipolytic enzyme according to or for us© in the present invention, the method comprising transforming a host cell with a recombinant nucleic acid comprising a nucleotide sequence coding for the fungal lipolytic enzyme according to or for use in the invention, the host cell being capable of " ' expressing the nucleotide sequence coding for the polypeptide of the ftmgal lipolytic en2yme, cultivating the transformed host eel! under conditions where (he nucleic acid is expressed and harvesting the fungal lipolytic enzyme.

In a further broad aspect, the invention provides a lipolytic enzyme which retains activity at low temperatures, i.e. is a low temperature lipolytic enzyme.

Aspects of the present invention are presented in the claims and in the following commentary.

Other aspects concerning the nucleotide sequences which can be used in the present invention include: a construct comprising the sequences of the present invention; a J3 m o m < m o an CO m ~o N> C3 CO Of: Ufa Hi i> Q* | N 548497 vector comprising the sequences for use in the present invention; a plasmid comprising the sequences for use in the present invention; a transformed cell comprising the sequences for use in the present invention; a transformed tissue comprising the sequences for use in the present invention; a transformed organ comprising the 5 sequences for use in the present invention; a transformed host comprising the sequences for use in the present invention; a transformed organism comprising the sequences for use in the present invention. The present invention also encompasses methods of expressing the nucleotide sequence for use in the present invention using the same, such as expression in a host cell; including methods for transferring same. 10 The present invention further encompasses methods of isolating the nucleotide sequence, such as isolating from a host cell.

Other aspects concerning the amino acid sequence for use in the present invention include: a construct encoding the amino acid sequences for use in the present invention; a 15 vector encoding the amino acid sequences for use in the present invention; a plasmid encoding the amino acid sequences for use in the present invention; a transformed cell expressing the amino acid sequences for use in the present invention; a transformed tissue expressing the amino acid sequences for use in the present invention; a transformed organ expressing the amino acid sequences for use in the present invention; a transformed host 20 expressing the amino acid sequences for use in the present invention; a transformed organism expressing the amino acid sequences for use in the present invention. The present invention also encompasses methods of purifying the amino acid sequence for use in the present invention using the same, such as expression in a host cell; including methods of transferring same, and then purifying said sequence.

For the ease of reference, these and further aspects of the present invention are now discussed under appropriate section headings. However, the teachings under each section are not necessarily limited to each particular section. 548497 7 DETAILED DISCLOSURE OF INVENTION la one aspect, the present invention provides a fungal lipolytic enzyme comprising an amino acid sequence as shown as SEQ ID No. 1, SEQ ED No. 2, SEQ ID No. 4, or 5 SEQ ID No. 6 or an amino acid sequence which has at least 90% identity thereto. In this specification the term "(fungal lipolytic) enzyme according to the invention" refers to the enzymes of this aspect and also wild-type fungal lipolytic enzymes having a higher ratio of activity on polar lipids compared with triglycerides.

In a further aspect the present invention provides a nucleic acid encoding a fungal lipolytic enzyme comprising an amino acid sequence as shown in SEQ ID No. 1, SEQ ED No. 2, SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity therewith.

SEQ ID No. 1 is shown in Figure 37, SEQ ID No. 2 is shown in Figure 38, SEQ ID No. 4 is shown in Figure 40 and SEQ ED No. 6 is shown in Figure 42.

In a further aspect the present invention provides a nucleic acid encoding a fungal lipolytic enzyme, which nucleic acid is selected from the group consisting of: 20 a) a nucleic acid comprising a nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7; b) a nucleic acid which is related to the nucleotide sequence of SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7 by the degeneration of the genetic code; and c) a nucleic acid comprising a nucleotide sequence which has at least 90% identity 25 with the nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7.

SEQ ID No. 3 is shown in Figure 39; SEQ ID No. 5 is shown in Figure 41; and SEQ ID No. 7 is shown in Figure 43.

In smother aspect the present invention provides the use of a fungal lipolytic enzyme according to the present invention in the manufacture of a foodstuff, such as for intellectual property office OF M Z- 1 6 SEP 2009 Dcr.cix/PO 548497 8 instance a dough, a baked product, an egg, an egg-based product, a noodle product, a cheese product, a tortilla product, an animal feed product, a vegetable oil or an edible oil. Advantageously, the addition, of an enzyme of the present invention to the foodstuff may lead to improved emulsification with lower accumulation of free fatty 5 acids.

In a further aspect the present invention provides the use of a fungal lipolytic enzyme according to the present invention in the manufacture of a dough and/or a baked product, comprising adding said lipolytic enzyme to a dough, and (optionally) baking the dough to make a baked product for one or more of the following: reducing stickiness of the dough; improving machinability of the dough; reducing blistering during baking of the baked product; improving bread volume and/or softness; prolonging shelf life of the baked product and/ox dough; improving antistaling effect of the baked product and/or dough; improving crumb structure of the baked product; reducing pore heterogeneity of the baked product; improving pore homogeneity of the baked product; reducing mean pore size of the baked product; enhancing the gluten index of the dough; improving flavour and/or odour of the baked product, improving the colour of the crust of the baked product.

Advantageously, the enzyme according to the present invention may have a higher activity than conventional lipolytic enzymes at a low pH and so may be more advantageously suited for use in a low pH sour dough environment than conventional lipolytic enzymes.

In another aspect of the present invention there is provided a method of making a dough and/or a baked product comprising adding a fungal lipolytic enzyme according to the present invention to a dough and (optionally) baking the dough to make the baked product.

In a further aspect of the present invention provides the use of a fungal lipolytic enzyme according to the present invention in the manufacture of egg-based products 548497 9 for improving texture, reducing mean particle size, reducing mean particle distribution, improving heat stability, improving microwave performance and/or stability.

In another aspect of the present invention, there is provided a method of treating egg or 5 egg-based product, which method comprises adding a fungal lipolytic enzyme according to the present invention to an egg or egg-based product.

In another aspect of the invention, there is provided a method of making noodles, or a noodle dough or a noodle-based product, which method comprises adding a fungal 10 lipolytic enzyme according to the present invention to the noodle, noodle dough or noodle-based product.

In one aspect of the present invention, there is provided a use of a fungal lipolytic enzyme according to the present invention in the manufacture of a noodle or a noodle-15 based product for one or more of improving colour/yellowness, stabilising colour characteristics, reducing brightness, reducing fat content, improving texture and bite (chewiness), reducing water activity, reducing breakage, increasing core firmness and improving shape retention during processing In another aspect of the invention, there is provided a method of making a tortilla or tortilla dough, which method comprises adding a fungal lipolytic enzyme according to the present invention to the tortilla or tortilla dough A further aspect of the present invention provides the use of a fungal lipolytic enzyme 25 according to the present invention in the manufacture of a tortilla or a tortilla dough for improving the reliability of a tortilla, increasing pliability of a tortilla, improving antistaling properties of the tortilla and/or tortilla dough, improving softness and/or reducing off-flavour in the tortilla and/or tortilla dough.

The functionality of the lipolytic enzyme in tortilla and/or noodles may be improved by combination with emulsifiers such as D ATEM. 548497 Iii another aspect of the invention, there is provided a method of treating milk, cheese milk, cheese or a cheese-based product, which method comprises adding a fungal lipolytic enzyme according to the present invention to the cheese or cheese-based product.

The present invention yet further provides use of a fungal lipolytic enzyme according to the present invention in the manufacture of a cheese or a cheese-based product for one or more of improving flavour, texture and/or stability, decreasing in the oiling-off effect in cheese and/or to increase cheese yield in cheese production.

In another aspect of the invention, there is provided a method of treating animal feed, which method comprises adding a fungal lipolytic enzyme according to the present invention to the animal feed.

The present invention further provides the use of a fungal lipolytic enzyme according to the present invention in the manufacture of animal feed for enhancing one or more of: feed utilisation and/or conversion efficiency, body weight gain, digestibility nitrogen uptake, metabolisability of dry matter and palatability.

In a further aspect of the present invention provides the use of a fungal lipolytic enzyme according to the present invention in a process of preparing a lyso-phospholipid, for example lysolecithin by treatment of a phospholipid (e.g. lecithin) with the enzyme to produce the partial hydrolysis product, i.e. the lyso-phospholipid.

In another aspect of the present invention there is provided a process of preparing a lyso-phospholipid, for example lysolecithin, which process comprises treating a phospholipid (e.g. lecithin) with the fungal lipolytic enzyme according to the present invention.

In a further aspect of the present invention provides the use of a fungal lipolytic enzyme according to the present invention in a process of preparing a lyso-glycolipid, 548497 II (for example digalactosyl monoglyceride (DGMG) or monogalactosyl monoglyceride (MGMG)) by treatment of a glycolipid (e.g. digalactosyl diglyceride (DGDG) or monogalactosyl diglyceride (MGDG)) with the lipolytic enzyme according to the present invention to produce the partial hydrolysis product, i.e. the lyso-glycolipid.

In a yet further aspect there is provided a process of preparing a lyso-glycolipid (for example digalactosyl monoglyceride (DGMG) or monogalactosyl monoglyceride (MGMG)), which process comprising treating a glycolipid (e.g. digalactosyl diglyceride (DGDG) or monogalactosyl diglyceride (MGDG)) with a fungal lipolytic 10 enzyme according to the present invention.

The present invention also provides a process of enzymatic degumming of vegetable or edible oils, comprising treating the edible ox vegetable oil with fungal lipolytic enzyme according to the present invention so as to hydrolyse a major part of the polar 15 lipids (e.g. phospholipid and/or glycolipid).

For the avoidance of doubt, a person of ordinary skill in the art would be aware of methodology suitable for carrying out the enzymatic treatment of edible oils (for instance see EP 0 869 167). Known method may suitably be used when carrying out 20 the present invention, with the proviso that the known enzyme is replaced with the enzyme according to the present invention.

In a further aspect the present invention provides the use of a fungal lipolytic enzyme according to the present invention in the manufacture of a vegetable oil or edible oil 25 for reducing the amount phospholipid in the vegetable oil or edible oil whilst maintaining the triglyceride content of the oil and/or preventing or reducing the accumulation of free fatty acids.

In a yet further aspect the present invention provides the use of a fungal lipolytic 30 enzyme according to the present invention in a process comprising treatment of a phospholipid so as to hydrolyse fatty acyl groups. 548497 12 In another aspect the present invention provides the use of a fungal lipolytic enzyme according to the present invention in a process for reducing the content of a phospholipid in an edible oil, comprising treating the oil with the fungal lipolytic enzyme according to the present invention so as to hydrolyse a major part of the 5 phospholipid, and separating an aqueous phase containing the hydrolysed phospholipid from the oil.

In a further aspect the invention provides a lipolytic enzyme which retains activity at low temperatures, i.e. a low temperature lipolytic enzyme. Further aspects of the 10 invention include the use of a low temperature lipolytic enzyme in the methods and uses describes herein, i.e. of the fungal lipolytic enzyme of the present invention.

Preferably, the fungal lipolytic enzyme according to the present invention has a higher ratio of activity on polar lipids (e.g. glycolipids and/or phospholipids) than on 15 triglycerides.

Preferably, the fungal lipolytic enzyme according to the present invention has a higlier ratio of activity on phospholipids than on triglycerides.

Preferably, the fungal lipolytic enzyme according to the present invention has a higher ratio of activity on glycolipids than on triglycerides.

Suitably, the fimgal lipolytic enzyme according to the present invention may have a higher ratio of activity on both glycolipids and phospholipids than on triglycerides.

More preferably, the fungal lipolytic enzyme according to the present invention has a higher ratio of activity on digalactosyl diglyceride (DGDG) than on triglycerides.

Preferably the fungal lipolytic enzyme according to the present invention hydrolyses 30 DGDG or MGDG to DGMG or MGMG, respectively. 548497 13 The term "higher ratio of activity on polar lipids" as referred to herein means that the fungal lipolytic enzyme according to the present invention has a polar lipid:triglyceride hydrolysing activity ratio which is higher when compared with a commercial enzyme Lipopan F™ (Novozymes A/S, Denmark).

The term "polar lipids" as used herein means phospholipids and/or glycolipids. Preferably the term "polar lipids" as used herein means both phospholipids and glycolipids.

The terms "higher ratio of activity on glycolipids" and "higher ratio of activity of phospholipids" as referred to herein means that the fungal lipolytic enzyme according to the present invention has a glycolipiditriglyceride hydrolysing activity ratio or a phospholipid:triglyceride hydrolysing activity ratio, respectively, which is higher than the corresponding ratio achieved with the commercial enzyme Lipopan F™ 15 (Novozymes A/S, Denmark).

Preferably, the lipolytic enzyme according to the present invention may have a polar lipid:triglyceride hydrolysing activity ratio of at least 4. Suitably, the polar lipid:triglyceride hydrolysing activity ratio may be greater than 5. Suitably, the polar 20 lipid:triglyceride hydrolysing activity ratio may be greater than 8, preferably greater than 9, more preferably greater than 10, even more preferably greater than 15.

Preferably, the fungal lipolytic enzyme according to the present invention may have a phospholipidrtriglyceride hydrolysing activity ratio of at least 4. Suitably, the polar 25 lipidrtriglyceride hydrolysing activity ratio may be greater than 5. Suitably, the polar iipid:triglyceride hydrolysing activity ratio may be greater than 8, preferably greater than 9, more preferably greater than 10, even more preferably greater than 15.

Preferably, the fungal lipolytic enzyme according to the present invention may have a 30 glycolipid:triglyceride hydrolysing activity ratio of at least 1.5, preferably at least 1.8, preferably at least 2, preferably at least 3, preferably at least 4. Suitably, the 548497 WO 2005/087918 PCT/IB2005/000875 14 glycolipid;triglyceride hydrolysing activity ratio may be greater than 4. Suitably, the glycolipid:triglyceride hydrolysing activity ratio may be greater than 5.

In a further aspect the present invention provides a fungal lipolytic enzyme having a 5 polar lipidrtriglyceride hydrolysing activity ratio of at least 4. Suitably, the polar lipid:triglyceride hydrolysing activity ratio may be greater than 5. Suitably, the polar lipidrtriglyceride hydrolysing activity ratio may be greater than 8, preferably greater than 9, more preferably greater than 10, even more preferably greater than 15.

In another aspect the present invention provides a fungal lipolytic enzyme having a phospholipid:triglyceride hydrolysing activity ratio of at least 4. Suitably, the polar lipid:triglyceride hydrolysing activity ratio may be greater than 5. Suitably, the polar lipidrtriglyceride hydrolysing activity ratio may be greater than 8, preferably greater than 9, more preferably greater than 10, even more preferably greater than 15.

In a yet further aspect, the present invention provides a fungal lipolytic enzyme having a glycolipidrtriglyceride hydrolysing activity ratio of at least 1.5, preferably at least 1.8, preferably at least 2, preferably at least 3, preferably at least 4, preferably greater than 5, preferably greater than 10, preferably greater than 15.

Preferably the fungal lipolytic enzyme according to the present invention has at least 1.5 times more activity against polar lipids (e.g. phospholipase A2 (E.C. 3.1.1.4) activity and/or phospholipase AI (E.C. 3.1.1.32) activity and/or glycolipase (E.C. 3.1.1.26) activity) as compared with triglyceride lipase activity (E.C. 3.1.1.3), more 25 preferably at least 2-times, more preferably at least 3-times, more preferably at least 4-times.

Preferably the fungal lipolytic enzyme according to the present invention has at least 1.5 times more glycolipase (E.C. 3.1.1.26) activity as compared with triglyceride 30 lipase activity (E.C. 3.1.1.3), more preferably at least 2-times, more preferably at least 3-times, more preferably at least 4-times. 548497 Preferably at the dosage that provides the optimal bread volume using the minibaking assay detailed in example 3, the ratio of hydrolysis of DGDG to triglyceride (TG) ratio is at least 1.7%, preferably at least 1.8%, preferably at least 2% preferably at least 3%, preferably at least 4%, preferably at least 5%, preferably at least 10%, preferably at 5 least 20%, preferably at least 40%, preferably at least 50%.

The term "glycolipase activity" as used herein encompasses "galactolipase activity".

The glycolipase activity, phospholipase activity and triacylglyceride lipase activity of 10 an enzyme can be determined using the assays presented hereinbelow.

Determination of galactolipase activity (glycolipase activity assay): Substrate: 0.6% digalactosyldiglyceride (Sigma D 4651), 0.4% Triton-X 100 (Sigma X-100) 15 and 5 mM CaCk was dissolved in 0.05M HEPES buffer pH 7.

Assay procedure: 400 uL substrate was added to an 1.5 mL Eppendorf tube and placed in an Eppendorf Thermomixer at 37°C for 5 minutes. At time t= 0 min, 50 jiL enzyme solution was added. Also a blank with water instead of enzyme was analyzed. The sample was 20 mixed at 10*100 rpm in an Eppendorf Thermomixer at 37°C for 10 minutes. At time t=10 min the Eppendorf tube was placed in another thermomixer at 99°C for 10 minutes to stop the reaction.

Free fatty acid in the samples was analyzed by using the NEFA C kit from WAKO GmbH.

Enzyme activity GLU at pH 7 was calculated as micromoles of fatty acid produced per minute under assay conditions.

Determination of phospholipase activity (phospholipase activity assay): Phospholipase activity was measured using two different methods which give comparable results. Either of these methods can be used to determine phospholipase 548497 16 activity in accordance with the present invention. Preferably, the PLU assay is used for determining the phospholipase activity of any enzyme.

"PLU assay" for determination of phospholipase activity Substrate: 0.6% L-a Phosphatidylcholine 95% Plant (Avanti #441601), 0.4% Triton-X 100 (Sigma X-100) and 5 mM CaCb was dissolved in 0.05M HEPES buffer pH 7. 10 Assay procedure: 400 pL substrate was added to an 1.5 mL Eppendorf tube and placed in an Eppendorf Thermomixer at 37°C for 5 minutes. At time t= 0 min, 50 pL enzyme solution was added. Also a blank with water instead of enzyme was analyzed. The sample was mixed at 10*100 rpmin an Eppendorf Thermomixer at 37°C for 10 minutes. At time 15 t=T0 min the Eppendorf tube was placed in another thermomixer at 99°C for 10 minutes to stop the reaction.

Free fatty acid in the samples was analyzed by using the NEFA C kit from WAKO GmbH.

Enzyme activity PLU-7 at pH 7 was calculated as micromoles of fatty acid produced 20 per minute under assay conditions "TIPU assay" for determination of phospholipase activity 1 TIPU (Titration Phospholipase Unit) is defined as the amount of enzyme, which 25 liberates 1 umol free fatty acid per minute at the assay conditions.

Phospholipase AI and A2 catalyse the conversion of lecithin to lyso-lecithin with release of the free fatty acid from position 1 and 2, respectively. Phospholipase activity can be determined by continous titration of the fatty acids liberated from lecithin 30 during enzymation, since the consumption of alkali equals the amount of fatty acid liberated. 548497 17 Substrate: 4% lecithin, 4% Triton-X 100, and 6 mM CaC12: 12 g lecithin powder (Avanti Polar Lipids #44160) and 12 g Triton-X 100 (Merck 108643) was dispersed in approx. 200 ml demineralised water during magnetic stirring. 3.0 ml 0.6 M CaC12 (p.a. Merck 5 1.02382) was added. The volume was adjusted to 300 mL with demineralised water and the emulsion was homogenised using an Ultra Thurax. The substrate was prepared freshly every day.

Assay procedure: An enzyme solution was prepared to give a slope on the titration curve between 0.06 and 0.18 ml/min with an addition of 300 |J.L enzyme.

A control sample of known activity is included.

The samples were dissolved in demineralised water and stirred for 15 min. at 300 rpm.

A .00 ml substrate was thermostatted to 37.0 C for 10-15 minutes before pH was 15 adjusted to 7.0 with 0,05 M NaOH. 300 jiL enzyme solution was added to the substrate and the continuous titration with 0.05 M NaOH was carried out using a pH-Stat titrator (Phm 290, Mettler Toledo). Two activity determinations are made on each scaling. After 8 minutes the titration is stopped and the slope of the titration curve is calculated between 5 and 7 minutes. The detection limit is 3 TIPU/ml enzyme solution.

Calculations: The phospholipase activity (TIPU/g enzyme) was calculated in the following way: TIPU/g= mol ml _a-N-10 -V, m • V2 m ■ V2 Where: a is the slope of the titration curve between 5 and 7 minutes of reaction time (ml/min) N is the normality of the NaOH used (mol/1) VI is the volume in which the enzyme is dissolved (ml) 548497 18 m is the amount of enzyme added to VI (g) V2 is the volume of enzyme solution added to the substrate (ml) Determination of triacylglyceride lipase activity: assay based on triglyceride (tributyrin) as substrate (LIPU): Lipase activity based on tributyrin is measured according to Food Chemical Codex, Forth Edition, National Academy Press, 1996, p 803, ith the modifications that the 10 sample is dissolved in deionized water instead of glycine buffer, and the pH stat set point is 5.5 instead of 7. 1 LIPU is defined as the quantity of enzyme which can liberate 1 mol butyric acid per minute under assay conditions.

Based on the assays for activity on galactolipid (GLU), phospholipid (PLU) and triglyceride (LIPU) it is possible to calculate the ratios PLU/LIPU and GLU/LIPU.

The analysis of Lipopan F™ and a lipolytic enzyme according to the present invention derived from Fusarium heterosporum (sample 209) (see Example 3) gave the 20 following results.

The relative activity ratios for Lipopan F™ and Sample 209 are Lipopan F Sample 209 Phospholipid/triglyceride PLU/LIPU 3 9 Galactolipid/triglyceride GLU/LIPU 1 4 Suitably the terms "synergy" or "synergistic effect" as used herein means that the combination produces a better effect than when each component (i.e. enzyme) is used separately. Synergy may be determined by making a product, e.g. a dough and/or baked product, with the addition of each component (i.e. enzyme) separately and in 30 combination, and comparing the effects. 548497 19 The term "fungal lipolytic enzyme" as used herein means that the naturally-occurring source of the enzyme is a fungus. For the avoidance of doubt, however, this term may include a ftmgal enzyme which is isolated from a fungus, one which is expressed in a 5 fungal host (either the native or non-native fungus) or one which is expressed in a non-fungal host (e.g. in a bacterial or yeast for instance).

Preferably, the fungal lipolytic enzyme according to the present invention is a wild type enzyme.

The terms "natural" and "wild type" as used herein mean a naturally-occurring enzyme. That is to say an enzyme expressed from the endogenous genetic code and isolated from its endogenous host organism and/or a heterologously produced enzyme which has not been mutated (i.e. does not contain amino acid deletions, additions or 15 substitutions) when compared with the mature protein sequence (after co- and post-translational cleavage events) endogenously produced. Natural and wild-type proteins of the present invention may be encoded by codon optimised polynucleotides for heterologous expression, and may also comprise a non-endogenous signal peptide selected for expression in that host The term "non-endogenous signal peptide" as used herein means a signal peptide not naturally present in the nascent polypeptide chain of the lipolytic enzyme prior to co-translational cleavage. In the lipolytic enzyme according to the present invention, part or whole of the non-endogenous signal peptide, for example a pro-peptide, may remain 25 attached to the mature polypeptide - this is encompassed by the term "wild-type" as used herein.

As mentioned above, the terms "natural" and "wild type" as used herein mean a naturally-occurring enzyme. However, this does not exclude the use of a synthetic or 30 chemically synthesised polypeptide comprising of the same polypeptide sequence as the naturally occuring mature lipolytic enzyme. 548497 The term "variant" as used herein means a protein expressed from a non-endogenous genetic code resulting in one or more axaino acid alterations (i.e. amino acid deletions, additions or substitutions) when compared with the natural or wild-type sequence within the mature protein sequence.

Preferably the fungal lipolytic enzyme according to the present invention is a lipolytic enzyme which retains activity at a low temperature, i.e. is a low temperature lipolytic enzyme.

The term "a low temperature lipolytic enzyme" means an enzyme which has significant activity at 5-15°C, preferably an enzyme which has significant activity at 10°C.

In one embodiment the low temperature lipolytic enzyme according to the present 15 invention is not a lipolytic enzyme comprising the amino acid sequence motif GDSX as disclosed in W02004/064987 wherein X is one or more of the following amino acid residues: L, A, V, I, F, Y, H, Q, T, N, M or S.

A low temperature lipolytic enzyme according to the present invention may be an 20 enzyme which has a relative activity of at least 5%, preferably at least 7%, more preferably at least 10%, on lecithin substrate at 10°C, at a pH within 20% of the optimal pH of the lipolytic enzyme, as determined by the determination of free fatty acids by the NEFA C method (see Example 5, performed at pH 7). Example 6 provides a method for determining the pH optima for a lipolytic enzyme.

A low temperature lipolytic enzyme according to the present invention may be an enzyme which has a relative activity of at least 10%, preferably at least 15%, more preferably at least 20%, more preferably at least 25% and most preferably at least 30% on lecithin substrated at 20°C, at a pH within 20% of the optimal pH of the lipolytic 30 enzyme, as determined by the determination of free fatty acids by the NEFA C method (see Example 5, performed at pH 7). Example 6 provides a method for determining the pH optima for a lipolytic enzyme. 548497 21 A low temperature lipolytic enzyme according to the present invention may also show significant activity of egg yolk lecithin at 5°C, characterised in that it is capable of releasing at least 1%, preferably at least 1.5%, more preferably at least 2% of free fatty 5 acid after a reaction time of 480 minutes at an enzyme dosage equivalent to 20 U/g egg yolk, using the assay described in Example 9 and illustrated in figures 24 and 25.

Preferably, the fungal lipolytic enzyme according to the present invention may be obtainable (preferably obtained) from a filamentous fungus. More preferably, the 10 fungal lipolytic enzyme is obtainable (preferably obtained) from Fusarium spp. Preferably, the fungal lipolytic enzyme according to the present invention may be obtainable (preferably obtained) from Fusarium heterosporum or Fusarium semitectum. Suitably, the fungal lipolytic enzyme according to the present invention may be obtainable (preferably obtained) from Fusarium heterosporum (CBS 782.83) 15 or Fusarium semitectum (IBT 9507).

Thus in one aspect, preferably the lipolytic enzyme according to the present invention is a filamentous fungal lipolytic enzyme, preferably a filamentous fungal wild-type lipolytic enzyme.

Preferably, the fungal lipolytic enzyme according to the present invention comprises an amino acid sequence which has at least 90%, preferably at least 95%, preferably at least 98%, preferably at least 99% identity with the amino acid sequence shown as SEQ ID No. 1 or SEQ ID No. 2, SEQ ID No. 4 or SEQ ID No.6.

Preferably, the nucleic acid encoding the fungal lipolytic enzyme according to the present invention comprises a nucleotide sequence which has at least 90%, preferably at least 95%, preferably at least 98%, preferably at least 99% identity with the nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7.

Preferably, the fungal lipolytic enzyme according to the present invention is not a fusion protein comprising an amino acid sequence from a Thermomyces protein or part 548497 WO 2005/087918 PCT/IB2005/000875 22 thereof fused with an amino acid sequence from a Fusarium protein or part thereof. In particular, preferably the fungal lipolytic enzyme according to the present invention is not a fusion protein comprising an amino acid sequence from a Thermomyces lanuginosa protein or a part thereof fused with an amino acid sequence from a 5 Fusarium oxysporum protein or part thereof.

Preferably, the ftmgal lipolytic enzyme according to the present invention is not obtained from Thermomyces lanuginosa and/or is not a variant of an enzyme obtained from Thermomyces lanuginosa.

Preferably, the fungal lipolytic enzyme according to the present invention is isolated from a fermentation broth of Fusarium heterosporum CBS 782.83 or Fusarium semitectum (IBT 9507).

Suitably, the enzyme may be purified by liquid chromatography.

The amino acid sequence of the purified fungal lipolytic enzyme may be determined by Edman degradation and MALDI-TOF analysis.

A partly purified lipolytic enzyme from Fusarium heterosporum CBS 782.83 has been tested in mini scale baking tests and in pilot scale baking tests with very good results.

The baking effects of the fungal lipolytic enzyme from F. heterosporum CBS 782.83 were found to be superior to Lipopan F™ and this correlated to a increased ratio of 25 activity on polar lipids, in particular glycolipids, such as digalactosyl diglyceride (DGDG), compared to triglycerides.

Additionally, a lipolytic enzyme from Fusarium semitectum IBT 9507 has been tested for activity on flour lipids in dough slurry with very good results. 548497 23 The lipolytic enzyme from F. semitectum IBT 9507 was shown to have significant activity on galactolipids in a dough and relatively less activity on triglyceride compared with Lipopan F™.

Suitably, the term "foodstuff' as used herein means a substance which is suitable for human and/or animal consumption.

Suitably, the term "foodstuff" as used herein may mean a foodstuff in a form which is ready for consumption. Alternatively or in addition, however, the term foodstuff as 10 used herein may mean one or more food materials which are used in the preparation of a foodstuff. By way of example only, the term foodstuff encompasses both baked goods produced from dough as well as the dough used in the preparation of said baked goods.

In a preferred aspect the present invention provides a foodstuff as defined above wherein the foodstuff is selected from one or more of the following: eggs, egg-based products, including but not limited to mayonnaise, salad dressings, sauces, ice creams, egg powder, modified egg yolk and products made therefrom; baked goods, including breads, cakes, sweet dough products, laminated doughs, liquid batters, muffins, 20 doughnuts, biscuits, crackers and cookies; confectionery, including chocolate, candies, caramels, halawa, gums, including sugar free and sugar sweetened gums, bubble gum, soft bubble gum, chewing gum and puddings; frozen products including sorbets, preferably frozen dairy products, including ice cream and ice milk; dairy products, including cheese, butter, milk, coffee cream, whipped cream, custard cream, milk 25 drinks and yoghurts; mousses, whipped vegetable creams; edible oils and fats, aerated and non-aerated whipped products, oil-in-water emulsions, water-in-oil emulsions, margarine, shortening and spreads including low fat and very low fat spreads; dressings, mayonnaise, dips, cream based sauces, cream based soups, beverages, spice emulsions and sauces.

In one aspect the foodstuff in accordance with the present invention may be a dough product or a baked product, such as a bread, a fried product, a snack, cakes, pies, 548497 24 brownies, cookies, noodles, instant noodles, tortillas, snack items such as crackers, graham crackers, pretzels, and potato chips, and pasta.

In another aspect, the foodstuff in accordance with the present invention may be an 5 animal feed.

In one aspect preferably the foodstuff is selected from one or more of the following: eggs, egg-based products, including mayonnaise, salad dressings, sauces, ice cream, egg powder, modified egg yolk and products made therefrom.

In some of the applications mentioned herein, particularly the food applications, such as the bakery applications, the lipolytic enzyme according to the present invention may be used with one or more conventional emulsifiers, including for example monoglycerides, diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, 15 sodium stearoyl lactylate (SSL) and lecithins.

The lipolytic enzyme according to the present invention is especially preferred in bread recipes with added fat; this is considered to be due to the low activity of the lipolytic enzyme according to the present invention on triglycerides which results in a 20 reduced free fatty acid accumulation and, with respect to short chain triglycerides, reduced or avoidance of off odour.

In the present context, the term "added fat" is used to indicate no lipid or fat is added to the flour dough.

In addition or alternatively, the enzyme according to the present invention may be used with one or more other suitable food grade enzymes. Thus, it is within the scope of the present invention that, in addition to the lipolytic enzyme of the present invention, at least one further enzyme may be added to the baked product and/or the dough. Such 30 further enzymes include starch degrading enzymes such as endo- or exoamylases, pullulanases, debranching enzymes, hemicellulases including xylanases, cellulases, oxidoreductases, e.g. glucose oxidase, pyranose oxidase, sulfhydryl oxidase or a 548497 carbohydrate oxidase such as one which oxidises maltose, for example hexose oxidase (HOX), lipases, phospholipases and hexose oxidase, proteases, and acyltransferases (such as those described in W004/064987 for instance).

It is particularly preferred that the lipolytic enzyme of the invention is used in combination with alpha amylases in producing food products. In particular, the amylase may be a non-maltogenic amylase, such as a polypeptide having non-maltogenic exoamylase activity, in particular, glucan 1,4-alpha-maltotetrahydrolase (EC 3.2. 1.60) activity (as disclosed in W005/003339). A suitable non-maltogenic 10 amylase is commercially available as Powersoft™ (available from Danisco A/S, Denmark). Maltogenic amylases such as Novamyl™ (Novozymes A/S, Denmark) may also be used. In one embodiment, the combined use of alpha amylases and the lipolytic enzyme of the invention may be used in a dough, and/or the production of a baked product, such as bread, cakes, doughnuts, cake doughnuts or bagels. The 15 combination of alpha amylases and the lipolytic enzyme of the invention is also considered as preferable for use in methods of production of tortillas, such as wheat and/or maize tortillas.

In another preferred embodiment, the lipolytic enzyme according to the present 20 invention may be used in combination with a xylanase in producing food products. GRINDAMYL™ and POWERBake 7000 are examples of commercially available xylanase enzymes available from Danisco A/S. Other examples of xylanase enzymes may be found in W003/020923 and WOOl/42433 Preferably, the lipolytic enzyme according to the present invention may be used in combination with a xylanase and an alpha amylase. Suitably the alpha amylase may be a maltogenic, or a non-maltogenic alpha amylase (such as GRINDAMYL™ or POWERSoft, commercially available from Danisco A/S), or a combination thereof.

The lipolytic enzyme of the invention can also preferably be used in combination with an oxidising enzyme, such as a maltose oxidising enzyme (MOX), for example hexose oxidase (HOX). Suitable methods are described in W003/099016. Commercially 548497 26 available maltose oxidising enzymes GRINDAMYL™ and SUREBake are available from Danisco A/S.

Optionally an alpha-amylase, such as a non-maltogenic cxoamylase and/or a 5 maltogenic amylases, and/or a maltose oxidising enzyme (MOX) in combination with the enzyme according to the present invention may be used in methods of preparing a dough, a baked product, tortilla, cake, instant noodle/fried snack food, or a dairy product such as cheese.

The lipolytic enzyme according to the present invention is typically included in the foodstuff or other composition by methods known in the art. Such methods include adding the lipolytic enzyme directly to the foodstuff or composition, addition of the lipolytic enzyme in combination with a stabilizer and/or carrier, and addition of a mixture comprising the lipolytic enzyme and a stabilizer and/or carrier.

Suitable stabilizers for use with the present invention include but is not limited to inorganic salts (such as NaCl, ammonium sulphate), sorbitol, emulsifiers and detergents (such as Tween 20, Tween 80, Panodan AB100 without triglycerides, polyglycerolester, sorbitanmonoleate), oil (such as rape seed oil, sunflower seed oil 20 and soy oil), pectin, trehalose and glycerol.

Suitable carriers for use with the present invention include but is not limited to starch, ground wheat, wheat flour, NaCl and citrate.

Gluten index may be measured by means of a Glutomatic 2200 from Perten Instruments (Sweden). To measure the gluten index: immediately after proofing, 15 g of dough may be scaled and placed in the Glutomatic and washed with 500 ml 2% NaCl solution for 10 min. The washed dough may then be transferred to a Gluten Index Centrifuge 2015 and the two gluten fractions scaled and the gluten index 30 calculated according to the following equation: Gluten index = (weight of gluten remaining on the sieve x 100)/total weight of gluten 548497 27 Preferably the gluten index in the dough is increased by at least 5%, relative to a dough without addition of the polypeptide, the gluten index may be determined by means of a Glutomatic 2200 apparatus mentioned above Further preferable aspects are presented in the accompanying claims and the in the following description and examples.

ADVANTAGES Surprisingly and unexpectedly it has been found that fungal lipolytic enzymes according to the present invention have a much higher ratio of activity on polar lipids (phospholipids and/or glycolipids).'triglycerides, compared with previously identified lipolytic enzymes (particularly LipopanF™) from fungi. This is particularly surprising 15 because prior to the present invention none of the known wild type lipolytic enzymes from fungi showed this activity. Although research had been carried out to investigate lipolytic enzyme variants (i.e. ones which had been exposed to non-natural mutagenesis and/or in some other way altered), it had not been envisaged that a natural, wild-type enzyme from fungi could have possessed these highly beneficial 20 characteristics.

The enzymes identified have been found to have superior functionality when used in baking applications. The use of the fungal lipolytic enzyme according to the present invention advantageously results in significantly improved properties to the dough 25 and/or baked products compared with other lipolytic enzymes from fungi, particularly LipopanF™.

Advantageously lipolytic enzyme which retains activity at lower temperatures, i.e. a low temperature lipolytic enzyme, may be suitable for use in low temperature 30 applications, thus removing the need to heat a substrate. This may be of particular advantage in applications such as enzymatic treatment of egg yolk, enzymatic degumming of edible oils, and in treatment of milk or dairy products, for example 548497 28 treatment of cheese milk prior to cheese manufacture. A further advantage of using a low temperature lipolytic enzyme may be found in foodstuffs and/or animal feeds, where the retention of significant activity at low operating temperatures allows for enzymatic treatment to be performed with reduced risk of microbial, particularly 5 bacterial, contamination. In addition, when the stability of the enzyme is greater at lower temperatures; this allows for efficient dosage of enzyme and longer effective working life of the enzyme in industrial applications.

TECHNICAL EFFECTS For baked products, such as bread, steam buns and US white pan bread, for example, the addition of a lipolytic enzyme of the present invention may result in one or more of the following: improved bread volume and softness, prolonged shelf life and/or an antistaling effect, improved crumb structure, reduced pore heterogeneity, reduced 15 mean pore size, enhanced gluten index, improved flavour and/or odour, and improved colour of the crust.

Advantageously, the enzyme according to the present invention may be used to replace emulsifiers in foodstuffs, such as dough and/or baked products.

The lipolytic enzyme according to the present invention may have synergy with emulsifiers such as DATEM, SSL, CSL, monoglyceride, polysorbates and Tween. Thus, the lipolytic enzyme according to the present invention may be used in combination with one or more emulsifiers. Advantageously, the use of the lipolytic 25 enzyme according to the present invention in combination with one or more emulsifiers may reduce the overall amount of emulsifier used compared with the amount needed when no enzyme according to the present invention is used.

The lipolytic enzyme according to the present invention may also have synergy with hydrocolloids, Guar, xanthum and pectin, and with maltose oxidising enzymes such as hexose oxidase. 548497 29 For doughnuts, cake doughnuts, bagels, snack cakes and muffins, for example, the use of a lipolytic enzyme of the present invention may result in a synergistic effect when used in combination with one or more of alpha-amylases, maltogenic alpha-amylase and non-maltogenic alpha-amylase.

For cakes, sponge cakes and palm cakes, for example, the use of the lipolytic enzyme of the present invention may result in a synergistic effect when used in combination with one or more of hydrocolioids such as Guar, and/or one or more emulsifiers such as DATEM.

For biscuits, for example, use of a lipolytic enzyme according to the present invention confers improved reliability and handling properties, particularly when cold (cold reliability).

Advantageously, in mayonnaise and other egg-based products, for example, use of a lipolytic enzyme according to the present invention may lead to improved texture, reduced mean particle size, and/or reduced mean particle distribution, improved heat stability, improved microwave performance and/or stability.

In calces, use of the present invention advantageously leads to improved softness, volume, improved keeping properties and shelf life.

For noodles or noodle-products, e.g. instant noodles, for example, the lipolytic enzyme of the present invention may confer one or more of the following characteristics: 25 improved colonr/yellowness, more stable colour characteristics, reduced brightness, reduced fat content, improved texture and bite (chewiness), reduced water activity, reduced breakage, increased core firmness and improved shape retention during processing.

Preferably, the lipolytic enzyme of the present invention may be used to reduce the fat content of a noodle or a noodle product, for instance an instant noodle. 548497 In tortilla, for example, use of the enzyme according to the present invention may result in one or more of the following: reduced reliability of the tortilla, for instance by increasing pliability, improved antistaling properties, improving softness and/or 5 reducing off flavour.

Advantageously, improved reliability and/or pliability may lead to a reduced likelihood of the tortilla splitting when rolled.

In cheese and/or cheese-based products, for example, the use of the enzyme according to the present invention may result in one or more of the following: an improved flavour, texture and/or stability, a decrease in the oiling-off effect in cheese and/or an increase in cheese yield.

The term "oiling off effect" as used herein refers to the free oil released when cheese is melted.

The lipolytic enzyme according to the present invention may be used to produce a low fat cheese. Advantageously, the enzyme of the present invention may stabilise fat in 20 milk and/or may enhance flavour.

One advantageous of the present invention is that the enzyme functions (and indeed has a high functionality) at a low temperature. This can have a number of advantages depending upon the use to which the enzyme is put. For instance, in cheese 25 manufacture this functionality may reduce the risk of microbial contamination and microbial growth during enzymatic treatment. The reason for this may be that the cheese can remain chilled during the enzymatic treatment. Thus, the lipolytic enzyme according of the present invention may be particularly suitable for maturation of cheese at low temperature for improved flavour.

In animal feed, for example, the enzyme according to the present invention advantageously may result in one or more the following: enhanced feed 548497 31 utilisation/conversion, efficiency within the animal, improved body weight gain of the animal, improved digestibility of the feed, improved nitrogen uptake by the animal, e.g. from the feed, improved metabolisability of dry matter of the feed and improved palatability of feed.

In degumming of an edible oil, such as a vegetable oil, the lipolytic enzyme of the present invention has a high activity at low temperature. This advantageously may reduce the requirement to heat oil prior to or during enzyme treatment. This has the advantageous effect of reducing the amount of energy needed effect the treatment. 10 The enzyme according to the present invention may improve selectivity the reduction of phospholipids compared with triglycerides. The enzyme according to the present invention in an edible oil (such as a vegetable oil) may there have reduced hydrolytic activity on triglycerides compared to phospholipids. This may lead to less of the triglyceride being hydrolysed (compared with a conventional/phospholipase enzyme) 15 and this may lead to fewer losses in the oil yield and/or a reduced free fatty acid accumulation in the oil (compared with a conventional lipolytic/phospholipase enzyme).

USES The enzyme according to the present invention has many applications.

In particular, the fungal lipolytic enzymes according to the present invention may be useful in the preparation of a foodstuff.

For example, the fungal lipoljtic enzymes according to the present invention may be particularly useful in the treatment of egg or egg-based products.

Phospholipases, particularly phospholipase A2 (E.C. 3.1.1.4), have been used for many 30 years for the treatment of egg or egg-based products (see US 4,034,124 and Dutihl & Groger 1981 J. Sci. Food Agric. 32, 451-458, for example). The phospholipase 548497 32 activity during the treatment of egg or egg-based products results in the accumulation of polar lysolecithin, which can act as an emulsifier.

Treatment of egg or egg-based products with a fungal lipolytic enzyme according to 5 the present invention can improve the stability, thermal stability under heat treatment such as pasteurisation and result in substantial thickening. Egg-based products may include, but are not limited to cakes, mayonnaise, salad dressings, sauces, ice creams and the like.

The fungal lipolytic enzymes according to the present invention are particularly useful in the preparation of baked products, such as those prepared from a dough, including breads, cakes, sweet dough products, laminated doughs, liquid batters, muffins, doughnuts, biscuits, crackers and cookies.

The fungal lipolytic enzymes according to the present invention may also be used in bread-improving additive, e.g. dough compositions, dough additive, dough conditioners, pie-mixes and similar preparations conventionally added to the flour and/or the dough during processes for making bread or other baked products to provide improved properties to the bread or other baked products.

Thus, the present invention further relates to a bread-improving composition and/or a dough-improving composition comprising a fungal lipolytic enzyme according to the present invention; and also to a dough or baked product comprising such a bread-improving and/or dough-improving composition.

The bread-improving composition and/or dough-improving composition may comprise, in addition to a fungal lipolytic enzyme according to the present invention, other substances, which substances are conventionally used in baking to improve the properties of dough and/or baked products. 548497 33 The bread-improving composition and/or dough-improving composition may comprise one or more conventional baking agents, such as one or more of the following constituents: A milk powder, gluten, an emulsifier, granulated fat, an oxidant, an amino acid, a 5 sugar, a salt, flour or starch.

Examples of suitable emulsifiers are: monoglycerides, diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, sugar esters, sodium stearoyl lactylate (SSL) and lecithins.

The bread and/or dough improving composition may further comprise another enzyme, such as one or more other suitable food grade enzymes, including starch degrading enzymes such as endo- or exoamylases, pullulanases, debranching enzymes, hemieellulases including xylanases, cellulases, oxidoreductases, e.g. glucose oxidase, 15 pyranose oxidase, sulfhydryl oxidase or a carbohydrate oxidase such as one which oxidises maltose, for example hexose oxidase (HOX), lipases, phospholipases and hexose oxidase, proteases and acyltransferases (such as those described in W004/064987 for instance).

The term "improved properties" as used herein means any property which may be improved by the action of tire fungal lipolytic enzymes of the present invention. In particular, the use of a fungal lipolytic enzyme according to the present invention results in one or more of the following characteristics: increased volume of the baked product; improved crumb structure of the baked product; anti-staling properties in the 25 baked product; increased strength, increased stability, reduced stickiness and/or improved machinability of the dough.

The improved properties are evaluated by comparison with a dough and/or a baked product prepared without addition of the lipolytic enzyme according to the present 30 invention. 548497 34 The term "baked product" as used herein includes a product prepared from a dough. Examples of baked products (whether of white, light or dark type) which may be advantageously produced by the present invention include one or more of the following: bread (including white, whole-meal and rye bread), typically in the form of 5 loaves or rolls or toast, French baguette-type bread, pitta bread, tortillas, tacos, cakes, pancakes, biscuits, crisp bread, pasta, noodles and the like.

The dough in accordance with the present invention may be a leavened dough or a dough to be subjected to leavening. The dough may be leavened in various ways such 10 as by adding sodium bicarbonate or the like, or by adding a suitable yeast culture such as a culture of Saccharomyces cerevisiae (baker's yeast).

The present invention further relates to the use of fungal lipolytic enzymes in accordance with the present invention to produce a pasta dough, preferably prepared 15 from durum flour or a flour of comparable quality.

The fungal lipolytic enzymes according to the present invention are suitable for use in the en2ymatic degumming of vegetable or edible oils. In processing of vegetable or edible oil the edible or vegetable oil is treated with a fungal lipolytic enzyme 20 according to the present invention so as to hydrolyse a major part of the polar lipids (e.g. phospholipid and/or glycolipid). Preferably, the fatty acyl groups are hydrolysed from the polar lipids. The degumming process typically results in the reduction of the content of the polar lipids, particularly of phospholipids, in an edible oil due to hydrolysis of a major part (i.e. more than 50%) of the polar lipid, e.g. glycolipid and/or 25 phospholipid. Typically, the aqueous phase containing the hydrolysed polar lipid (e.g. phospholipid and/or glycolipid) is separated from the oil. Suitably, the edible or vegetable oil may initially (pre-treatment with the enzyme according to the present invention) have a phosphorus content of 50-250 ppm.

Furthermore, the present invention is directed to the use of a lipolytic enzyme according to the present invention for treatment of cheese products. 548497 The lipolytic enzyme according to the present invention is also particularly suitable for use in the preparation of an animal feed.

As the skilled person is aware, the term "degumming" as used herein means the 5 refining of oil by converting phosphatides (such as lecithin, phospoholipids and occluded oil) into hydratable phosphatides. Oil which has been degummed is more fluid and thus has better handling properties than oil which has not been degummed.

The following table is merely for general guidance and provides an overview of the 10 dosage level for a lipolytic enzyme according to the present invention which may be needed in different applications. The table further provides guidance in respect of the dosage level for a lipolytic enzyme according to the present invention when used in combination with an emulsifier for example. Of course, as would be apparent to the person of ordinary skill in the art optimisation of enzyme dosage, reaction temperature 15 and reaction time may be readily determined, using routine experimentation, for any given application.

Application "Optimal" dosage, TIPU/kg of flour Optimal dosage in combination with emulsifier Dosage range, TIPU/KG of flour Crusty rolls 400 120 300-800 Straight dough toast bread 400 120 300-800 Straight dough long fermentation 120 75-250 High speed mixing - Tweedy procedure 120 300-800 US sponge & dough pan bread on top of DATEM 120 75-400 548497 36 Wheat tortilla 700 Contains emulsifiers 400-2500 Cakes - sponge cakes 2000 Contains cake emulsifiers 1000-4000 Retarded dough (24 hours) 120 Contains emulsifiers 75-250 Steam buns 200 150-500 Instant fried noodles 200-10,000 ISOLATED In one aspect, preferably the sequence is in an isolated form. The term "isolated" means that the sequence is at least substantially free from at least one other component with which the sequence is naturally associated in nature and as found in nature.

PURIFIED In one aspect, preferably the sequence is in a purified form. The term "purified" means that the sequence is in a relatively pure state - e.g. at least about 90% pure, or at least about 95% pure or at least about 98% pure.

NUCLEOTIDE SEQUENCE The scope of the present invention encompasses nucleotide sequences encoding enzymes having the specific properties as defined herein.

The term "nucleotide sequence" as used herein refers to an oligonucleotide sequence or polynucleotide sequence, and variants, homologues, fragments and derivatives thereof (such as portions thereof). The nucleotide sequence may be of genomic or synthetic or 548497 37 recombinant origin, which may be double-stranded or single-stranded whether representing the sense or anti-sense strand.

The term "nucleotide sequence" in relation to the present invention includes genomic 5 DNA, cDNA, synthetic DNA, and RNA. Preferably it means DNA, more preferably cDNA sequence coding for the present invention.

In a preferred embodiment, the nucleotide sequence when relating to and when encompassed by the per se scope of the present invention does not include the native 10 nucleotide sequence according to the present invention when in its natural environment and when it is linked to its naturally associated sequence(s) that is/are also in its/their natural environment. For ease of reference, we shall call this preferred embodiment the "non-native nucleotide sequence". In this regard, the term "native nucleotide sequence" means an entire nucleotide sequence that is in its native environment and when 15 operatively linked to an entire promoter with which it is naturally associated, which promoter is also in its native environment. However, the amino acid sequence encompassed by scope the present invention can be isolated and/or purified post expression of a nucleotide sequence in its native organism. Preferably, however, the amino acid sequence encompassed by scope of the present invention may be expressed 20 by a nucleotide sequence in its native organism but wherein the nucleotide sequence is not under the control of the promoter with which it is naturally associated within that organism.

PREPARATION OF THE NUCLEOTIDE SEQUENCE Typically, the nucleotide sequence encompassed by scope of the present invention is prepared using recombinant DNA techniques (i.e. recombinant DNA). However, in an alternative embodiment of the invention, the nucleotide sequence could be synthesised, in whole or in part, using chemical'methods well known in the art (see Caruthers MH 30 et at, (1980) Nuc Acids Res Symp Ser 215-23 and Horn T et al„ (1980) Nuc Acids Res Symp Ser 225-232). 548497 38 A nucleotide sequence encoding an enzyme which has the specific properties as defined herein may be identified and/or isolated and/or purified from any cell or organism producing said enzyme. Various methods are well known within the art for the identification and/or isolation and/or purification of nucleotide sequences. By way 5 of example, PGR amplification techniques to prepare more of a sequence may be used once a suitable sequence has been identified and/or isolated and/or purified.

By way of farther example, a genomic DNA and/or cDNA library may be constructed using chromosomal DNA or messenger RNA from the organism producing the 10 enzyme. If the amino acid sequence of the enzyme or a part of the amino acid sequence of the enzyme is known, labelled oligonucleotide probes may be synthesised and used to identify enzyme-encoding clones from the genomic library prepared from the organism. Alternatively, a labelled oligonucleotide probe containing sequences homologous to another known enzyme gene could be used to identify enzyme-15 encoding clones. In the latter case, hybridisation and washing conditions of lower stringency are used.

Alternatively, enzyme-encoding clones could be identified by inserting fragments of genomic DNA into an expression vector, such as a plasmid, transforming enzyme-20 negative bacteria with the resulting genomic DNA library, and then plating the transformed bacteria onto agar plates containing a substrate - for the enzyme (e.g. maltose for a glucosidase (maltase) producing enzyme), thereby allowing clones expressing the enzyme to be identified.

In a yet further alternative, the nucleotide sequence encoding the enzyme may be prepared synthetically by established standard methods, e.g. the phosphoroamidite method described by Beucage S.L. et al, (1981) Tetrahedron Letters 22, p 1859-1869, or the method described by Matthes et al, (1984) EMBO J. 3, p 801-805. In the phosphoroamidite method, oligonucleotides are synthesised, e.g. in an automatic DNA 30 synthesiser, purified, annealed, ligated and cloned in appropriate vectors. 548497 39 The nucleotide sequence may be of mixed genomic and synthetic origin, mixed synthetic and cDNA origin, or mixed genomic and cDNA origin, prepared by ligating fragments of synthetic, genomic or cDNA origin (as appropriate) in accordance with standard techniques. Each ligated fragment corresponds to various parts of the entire 5 nucleotide sequence. The DNA sequence may also be prepared by polymerase chain reaction (PCR) using specific primers, for instance as described in US 4,683,202 or in Saiki R K et al, (Science (1988) 239, pp 487-491).

Due to degeneracy in the genetic code, nucleotide sequences may be readily produced 10 in which the triplet codon usage, for some or all of the amino acids encoded by the original nucleotide sequence, has been changed thereby producing a nucleotide sequence with low homology to the original nucleotide sequence but which encodes the same, or a variant, amino acid sequence as encoded by the original nucleotide sequence. For example, for most amino acids the degeneracy of the genetic code is at 15 the third position in the triplet codon (wobble position) (for reference see Stayer, Lubert, Biochemistry, Third Edition, Freeman Press, ISBN 0-7167-1920-7) therefore, a nucleotide sequence in which all triplet codons have been "wobbled" in the third position would be about 66% identical to the original nucleotide sequence. However, the amended nucleotide sequence would encode for the same, or a variant, primary 20 amino acid sequence as the original nucleotide sequence.

Therefore, the present invention farther relates to any nucleotide sequence that has alternative triplet codon usage for at least one amino acid encoding triplet codon, but which encodes the same, or a variant, polypeptide sequence as the polypeptide 25 sequence encoded by the original nucleotide sequence.

Furthermore, specific organisms typically have a bias as to which triplet codons are used to encode amino acids. Preferred codon usage tables are widely available, and can be used to prepare codon optimised genes. Such codon optimisation techniques 30 are routinely used to optimise expression of transgenes in a heterologous host. 548497 40 AMINO ACID SEQUENCES The scope of the present invention also encompasses amino acid sequences of enzymes having the specific properties as defined herein.

As used herein, the term "amino acid sequence" is synonymous with the term "polypeptide" and/or the term "protein". In some instances, the term "amino acid sequence" is synonymous with the term "peptide". In some instances, the term "amino acid sequence" is synonymous with the term "enzyme".

The amino acid sequence may be prepared/isolated from a suitable source, or it may be made synthetically or it may be prepared by use of recombinant DNA techniques.

The enzyme encompassed in the present invention may be used in conjunction with other 15 enzymes. Thus the present invention also covers a combination of enzymes wherein the combination comprises the enzyme of the present invention and another enzyme, which may be another enzyme according to the present invention.

Preferably the amino acid sequence when relating to and when encompassed by the per 20 se scope of the present invention is not a native enzyme. In this regard, the term "native enzyme" means an entire enzyme that is in its native environment and when it has been expressed by its native nucleotide sequence.

IDENTITY/HOMOLO G Y The present invention also encompasses the use of homologues of any amino acid sequence of an enzyme or of any nucleotide sequence encoding such an enzyme.

Here, the term "homologue" means an entity having a certain homology with the amino acid sequences and the nucleotide sequences. Here, the term "homology" can be equated with "identity". These terms will be used interchangeably herein. 548497 41 In the present context, a homologous amino acid sequence is taken to include an amino acid sequence which may be at least 92% identical, preferably at least 95, 96, 97,98 ox 99% identical to the sequence. Typically, the homologues will comprise the same active sites etc. - e.g. as the subject amino acid sequence. Although homology can also 5 be considered in terms of similarity (i.e. amino acid residues having similar chemical properties/functions), in the context of the present invention it is preferred to express homology in terms of sequence identity.

Preferably, an homologous amino acid sequence according to the present invention is 10 one which has at least 90% identity, more preferably at least 95, 96, 97, 98 or 99% identity, over a region of at least 30, more preferably 40, contiguous amino acids.

In the present context, an homologous nucleotide sequence is taken to include a nucleotide sequence which may be at least 92% identical, preferably at least 95, 96, 97, 15 98 or 99% identical to a nucleotide sequence encoding an enzyme of the present invention (the subject sequence). Typically, the homologues will comprise the same sequences that code for the active sites etc. as the subject sequence. Although homology can also be considered in terms of similarity (i.e. amino acid residues having similar chemical properties/functions), in the context of the present invention it 20 is preferred to express homology in terms of sequence identity.

Preferably, an homologous nucleotide sequence according to the present invention is one which has at least 90% identity, more preferably at least 95, 96, 97, 98 or 99% identity, over a region of at least 30, preferably 40, more preferably 60 contiguous nucleotides.

For the amino acid sequences and the nucleotide sequences, homology comparisons can be conducted by eye, or more usually, with the aid of readily available sequence comparison programs. These commercially available computer programs can calculate % homology between two or more sequences. % homology may be calculated over contiguous sequences, i.e. one sequence is aligned with the other sequence and each amino acid in one sequence is directly 548497 42 compared with the corresponding amino acid in the other sequence, one residue at a time. This is called an "ungapped" alignment. Typically, such ungapped alignments are performed only over a relatively short number of residues.

Although this is a very simple and consistent method, it fails to take into consideration that, for example, in an otherwise identical pair of sequences, one insertion or deletion will cause the following amino acid residues to be put out of alignment, thus potentially resulting in a large reduction in % homology when a global alignment is performed. Consequently, most sequence comparison methods are designed to 10 produce optimal alignments that take into consideration possible insertions and deletions without penalising unduly the overall homology score. This is achieved by inserting "gaps" in the sequence alignment to try to maximise local homology.

However, these more complex methods assign "gap penalties" to each gap that occurs 15 in the alignment so that, for the same number of identical amino acids, a sequence alignment with as few gaps as possible - reflecting higher relatedness between the two compared sequences - wall achieve a higher score than one with many gaps. "Affme gap costs" are typically used that charge a relatively high cost for the existence of a gap and a smaller penalty for each subsequent residue in the gap. This is the most 20 commonly used gap scoring system. High gap penalties will of course produce optimised alignments with fewer gaps. Most alignment programs allow the gap penalties to be modified. However, it is preferred to use the default values when using such software for sequence comparisons. For example when using the GCG Wisconsin Bestfit package the default gap penalty for amino acid sequences is -12 for 25 a gap and -4 for each extension.

Calculation of maximum % homology therefore firstly requires the production of an optimal alignment, taking into consideration gap penalties. A suitable computer program for carrying out such an alignment is the GCG Wisconsin Bestfit package 30 (Devereux et al 1984 Nuc. Acids Research 12 p387). Examples of other software than can perform sequence comparisons include, but are not limited to, the BLAST package (see Ausubel et al, 1999 Short Protocols in Molecular Biology, 4th Ed - Chapter 18), 548497 43 FASTA (Altschul et al, 1990 J Mol. Biol. 403-410) and the GENE WORKS suite of comparison tools. Both BLAST and FASTA are available for offline and online searching (see Ausubel et al., 1999, Short Protocols in Molecular Biology, pages 7-58 to 7-60).

However, for some applications, it is preferred to use the GCG Bestfit program. A new tool, called BLAST 2 Sequences is also available for comparing protein and nucleotide sequence (see FEMS Microbiol Lett 1999 174(2): 247-50; FEMS Microbiol Lett 1999 177(1): 187-8 and tatiana@ncbi.nlm.nih.gov).

Although the final % homology can be measured in terms of identity, the alignment process itself is typically not based on an all-or-nothing pair comparison. Instead, a scaled similarity score matrix is generally used that assigns scores to each pairwise comparison based on chemical similarity or evolutionary distance. An example of 15 such a matrix commonly used is the BLOSUM62 matrix - the default matrix for the BLAST suite of programs. GCG Wisconsin programs generally use either the public default values or a custom symbol comparison table if supplied (see user manual for further details). For some applications, it is preferred to use the public default values for the GCG package, or in the case of other software, the default matrix, such as 20 BLOSUM62.

Alternatively, percentage homologies may be calculated using the multiple alignment feature in DNASIS™ (Hitachi Software), based on an algorithm, analogous to CLUSTAL (Higgins DG & Sharp PM (1988), Gene 73(1), 237-244).

Once the software has produced an optimal alignment, it is possible to calculate % homology, preferably % sequence identity. The software typically does this as part of the sequence comparison and generates a numerical result.

The sequences may also have deletions, insertions or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent substance. Deliberate amino acid substitutions may be made on the basis of similarity 548497 44 in amino acid properties (such as polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues) and it is therefore useful to group amino acids together in functional groups. Amino acids can be grouped together based on the properties of their side chain alone. However it is more useful to 5 include mutation data as well. The sets of amino acids thus derived are likely to be conserved for structural reasons. These sets can be described in the form of a Venn diagram (Livingstone C.D. and Barton GJ. (1993) "Protein sequence alignments: a strategy for the hierarchical analysis of residue conservation" Comput.Appl Biosci. 9: 745-756)(Taylor W.R. (1986) "The classification of amino acid conservation" 10 J.Theor.Biol. 119; 205-218). Conservative substitutions may be made, for example according to the table below which describes a generally accepted Venn diagram grouping of amino acids.

SET SUB-SET Hydrophobic FWYHKMILVAGC Aromatic FWYH Aliphatic ILV Polar WYIIKREDCSTNQ Charged HKRED Positively charged HKR Negatively charged ED Small VCAGSPTND Tiny AGS The present invention also encompasses homologous substitution (substitution and replacement are both used herein to mean the interchange of an existing amino acid residue, with an alternative residue) that may occur i.e. like-for-like substitution such as basic for basic, acidic for acidic, polar for polar etc. Non-homologous substitution may also occur i.e. from one class of residue to another or alternatively involving the 20 inclusion of unnatural amino acids such as ornithine (hereinafter referred to as Z), diaminobutyric acid ornithine (hereinafter referred to as B), norleucine ornithine (hereinafter referred to as O), pyriylalanine, thienylalanine, naphthylalanine and 548497 45 phenylglycine.

Replacements may also be made by unnatural amino acids.

Variant amino acid sequences may include suitable spacer groups that may be inserted between any two amino acid residues of the sequence including alkyl groups such as methyl, ethyl or propyl groups in addition to amino acid spacers such as glycine or p-alanine residues. A further form of variation, involves the presence of one or more amino acid residues in peptoid form, will be well understood by those skilled in the art. 10 For the avoidance of doubt, "the peptoid form" is used to refer to variant amino acid residues wherein the a-carbon substituent group is on the residue's nitrogen atom rather than the a-carbon. Processes for preparing peptides in the peptoid form are known in the art, for example Simon RJ et al., PNAS (1992) 89(20), 9367-9371 and Horwell DC, Trends Biotechnol. (1995) 13(4), 132-134.

The nucleotide sequences for use in the present invention may include within them synthetic or modified nucleotides. A number of different types of modification to oligonucleotides are known in the art. These include methylphosphonate and phosphorothioate backbones and/or the addition of acridine or polylysine chains at the 20 3' and/or 5' ends of the molecule. For the purposes of the present invention, it is to be understood that the nucleotide sequences described herein may be modified by any method available in the art. Such modifications may be carried, out in order to enhance the in vivo activity or life span of nucleotide sequences of the present invention.

The present invention also encompasses the use of nucleotide sequences that are complementary to the sequences presented herein, or any derivative, fragment or derivative thereof. If the sequence is complementary to a fragment thereof then that sequence can be used as a probe to identify similar coding sequences in other organisms etc.

Polynucleotides which are not 100% homologous to the sequences of the present invention but fall within the scope of the invention can be obtained in a number of ways. 548497 46 Other variants of the sequences described herein may be obtained for example by probing DNA libraries made from a range of individuals, for example individuals from different populations. In addition, other homologues may be obtained and such homologues and fragments thereof in general will be capable of selectively hybridising to the sequences 5 shown in the sequence listing herein. Such sequences may be obtained by probing cDNA libraries made from or genomic DNA libraries from other species, and probing such libraries with probes comprising all or part of any one of the sequences in the attached sequence listings under conditions of medium to high stringency. Similar considerations apply to obtaining species homologues and allelic variants of the polypeptide or 10 nucleotide sequences of the invention.

Variants and strain/species homologues may also be obtained using degenerate PCR which will use primers designed to target sequences within the variants and homologues encoding conserved amino acid sequences within the sequences of the present invention. 15 Conserved sequences can be predicted, for example, by aligning the amino acid sequences from several variants/homologues. Sequence alignments can be performed using computer software known in the art. For example the GCG Wisconsin PileUp program is widely used.

The primers used in degenerate PCR will contain one or more degenerate positions and will be used at stringency conditions lower than those used for cloning sequences with single sequence primers against known sequences.

Alternatively, such polynucleotides may be obtained by site directed mutagenesis of 25 characterised sequences. This may be useful where for example silent codon sequence changes are required to optimise codon preferences for a particular host cell in which the polynucleotide sequences are being expressed. Other sequence changes may be desired in order to introduce restriction enzyme recognition sites, or to alter the property or function of the polypeptides encoded by the polynucleotides.

Polynucleotides (nucleotide sequences) of the invention may be used to produce a primer, e.g. a PCR primer, a primer for an alternative amplification reaction, a probe e.g. labelled 548497 47 with a revealing label by conventional means using radioactive or non-radioactive labels, or the polynucleotides may be cloned into vectors. Such primers, probes and other fragments will be at least 15, preferably at least 20, for example at least 25, 30 or 40 nucleotides in length, and are also encompassed by the term polynucleotides of the 5 invention as used herein.

Polynucleotides such as DNA polynucleotides and probes according to the invention may be produced recombinantly, synthetically, or by any means available to those of skill in the art. They may also be cloned by standard techniques.

In general, primers will be produced by synthetic means, involving a stepwise manufacture of the desired nucleic acid sequence one nucleotide at a time. Techniques for accomplishing this using automated techniques are readily available in the art.

Longer polynucleotides will generally be produced using recombinant means, for example using a PCR (polymerase chain reaction) cloning techniques. The primers may be designed to contain suitable restriction enzyme recognition sites so that the amplified DNA can be cloned into a suitable cloning vector.

BIOLOGICALLY ACTIVE Preferably, the variant sequences etc. are at least as biologically active as the sequences presented herein.

As used herein "biologically active" refers to a sequence having a similar structural function (but not necessarily to the same degree), and/or similar regulatory function (but not necessarily to the same degree), and/or similar biochemical function (but not necessarily to the same degree) of the naturally occurring sequence. 548497 48 HYBRIDISATION The present invention also encompasses sequences that are complementary to the nucleic acid sequences of the present invention or sequences that are capable of 5 hybridising either to the sequences of the present invention or to sequences that are complementary thereto.

The term "hybridisation" as used herein shall include "the process by which a strand of nucleic acid joins with a complementary strand through base pairing" as well as the 10 process of amplification as carried out in polymerase chain reaction (PCR) technologies.

The present invention also encompasses the use of nucleotide sequences that are capable of hybridising to the sequences that are complementary to the sequences 15 presented herein, or any derivative, fragment or derivative thereof.

The term "variant" also encompasses sequences that are complementary to sequences that are capable of hybridising to the nucleotide sequences presented herein.

Preferably, the term "variant" encompasses sequences that are complementary to sequences that are capable of hybridising under stringent conditions (e.g. 50°C and 0.2xSSC {lxSSC = 0.15 M NaCl, 0.015 M Na3citrate pH 7.0}) to the nucleotide sequences presented herein.

More preferably, the term "variant" encompasses sequences that axe complementary to sequences that are capable of hybridising under high stringent conditions (e.g. 65°C and O.lxSSC {lxSSC = 0.15 M NaCl, 0.015 M Na3citrate pH 7.0}) to the nucleotide sequences presented herein.

The present invention also relates to nucleotide sequences that can hybridise to the nucleotide sequences of the present invention (including complementary sequences of those presented herein). 548497 49 The present invention also relates to nucleotide sequences that are complementary to sequences that can hybridise to the nucleotide sequences of the present invention (including complementary sequences of those presented herein).

Also included within the scope of the present invention are polynucleotide sequences that are capable of hybridising to the nucleotide sequences presented herein under conditions of intermediate to maximal stringency.

In a preferred aspect, the present invention covers nucleotide sequences that can hybridise to the nucleotide sequence of the present invention, or the complement thereof, under stringent conditions (e.g. 50°C and 0.2xSSC).

In a more preferred aspect, the present invention covers nucleotide sequences that can 15 hybridise to the nucleotide sequence of the present invention, or the complement thereof, under high stringent conditions (e.g. 65°C and O.lxSSC).

RECOMBINANT In one aspect the sequence for use in the present invention is a recombinant sequence -i.e. a sequence that has been prepared using- recombinant DNA techniques.

These recombinant DNA techniques are within the capabilities of a person of ordinary skill in the art. Such techniques are explained in the literature, for example, J. Sambrook, 25 E. F. Fiitsch, and T. Maniatis, 1989, Molecular Cloning: A Laboratory Manual, Second Edition, Books 1-3, Cold Spring Harbor Laboratory Press.

SYNTHETIC In one aspect the sequence for use in the present invention is a synthetic sequence -i.e. a sequence that has been prepared by in vitro chemical or enzymatic synthesis. It 548497 50 includes, but is not limited to, sequences made with optimal codon usage for host organisms - such as the methylotrophic yeasts Pichia and Hansenula.

EXPRESSION OF ENZYMES The nucleotide sequence for use in the present invention may be incorporated into a recombinant replicable vector. The vector may be used to replicate and express the nucleotide sequence, in enzyme form, in and/or from a compatible host cell.

Expression may be controlled using control sequences e.g. regulatory sequences.

The enzyme produced by a host recombinant cell by expression of the nucleotide sequence may be secreted or may be contained intracellularly depending on the sequence and/or the vector used. The coding sequences may be designed with signal 15 sequences which direct secretion of the substance coding sequences through a particular prokaryotic or eukaryotic cell membrane.

EXPRESSION VECTOR The term "expression vector" means a construct capable of in vivo or in vitro expression.

Preferably, the expression vector is incorporated into the genome of a suitable host organism. The term "incorporated" preferably covers stable incorporation into the genome.

The nucleotide sequence of the present invention may be present in a vector in which the nucleotide sequence is operably linked to regulatory sequences capable of providing for the expression of the nucleotide sequence by a suitable host organism.

The vectors for use in the present invention may be transformed into a suitable host cell as described below to provide for expression of a polypeptide of the present invention. 548497 51 The choice of vector e.g. a plasmid, cosmid, or phage vector will often depend on the host cell into which it is to be introduced.

The vectors for use in the present invention may contain one or more selectable marker genes such as a gene which confers antibiotic resistance e.g. ampicillin, kanamycin, chloramphenicol or tetracyclin resistance. Alternatively, the selection may be accomplished by co-transformation (as described in W091/17243).

Vectors may be used in vitro, for example for the production of RNA or used to transfect, transform, transduce or infect a host cell.

Thus, in a further embodiment, the invention provides a method of making nucleotide sequences of the present invention by introducing a nucleotide sequence of the present 15 invention into a replicable vector, introducing the vector into a compatible host cell, and growing the host cell under conditions which bring about replication of the vector.

The vector may further comprise a nucleotide sequence enabling the vector to replicate in the host cell in question. Examples of such sequences are the origins of replication 20 of plasmids pUC19, pACYC177, pUBllO, pE194, pAMBl and pIJ702.

REGULATORY SEQUENCES In some applications, the nucleotide sequence for use in the present invention is 25 operably linked to a regulatory sequence which is capable of providing for the expression of the nucleotide sequence, such as by the chosen host cell. By way of example, the present invention covers a vector comprising the nucleotide sequence of the present invention operably linked to such a regulatory sequence, i.e. the vector is an expression vector.

The term "operably linked" refers to a juxtaposition wherein the components described are in a relationship permitting them to function in their intended manner. A 548497 52 regulatory sequence "operably linked" to a coding sequence is ligated in such a way that expression of the coding sequence is achieved under condition compatible with the control sequences.

The term "regulatory sequences" includes promoters and enhancers and other expression regulation signals.

The term "promoter" is used in the normal sense of the art, e.g. an RNA polymerase binding site.

Enhanced expression of the nucleotide sequence encoding the enzyme of the present invention may also be achieved by the selection of heterologous regulatory regions, e.g. promoter, secretion leader and terminator regions.

Preferably, the nucleotide sequence according to the present invention is operably linked to at least a promoter.

Examples of suitable promoters for directing the transcription of the nucleotide sequence in a bacterial, fungal or yeast host are well known in the art.

CONSTRUCTS The term "construct" - which is synonymous with terms such as "conjugate"., "cassette" 25 and "hybrid" - includes a nucleotide sequence for use according to the present invention directly or indirectly attached to a promoter.

An example of an indirect attachment is the provision of a suitable spacer group such as an intron sequence, such as the Shl-intron or the ADH intron, intermediate the promoter 30 and the nucleotide sequence of the present invention. The same is true for the term "fused" in relation to the present invention which includes direct or indirect attachment. In some cases, the terras do not cover the natural combination of the nucleotide sequence 548497 53 coding for the protein ordinarily associated with the wild type gene promoter and when they are both in their natural environment.

The construct may even contain or express a marker, which allows for the selection of the 5 genetic construct.

For some applications, preferably the construct of the present invention comprises at least the nucleotide sequence of the present invention operably linked to a promoter.

HOST CELLS The term "host cell" - in relation to the present invention includes any cell that comprises either the nucleotide sequence or an expression vector as described above 15 and which is used in the recombinant production of an enzyme having the specific properties as defined herein.

Thus, a further embodiment of the present invention provides host cells transformed or transfected with a nucleotide sequence that expresses the enzyme of the present 20 invention. The cells will be chosen to be compatible with the said vector and may for example be prokaryotic (for example bacterial), fungal, yeast or plant cells. Preferably, the host cells are not human cells.

Examples of suitable bacterial host organisms are gram positive or gram negative 25 bacterial species.

Depending on the nature of the nucleotide sequence encoding the enzyme of the present invention, and/or the desirability for further processing of the expressed protein, eukaryotic hosts such as yeasts or other fungi may be preferred. In general, 30 yeast cells are preferred over fungal cells because they are easier to manipulate. However, some proteins are either poorly secreted from the yeast cell, or in some cases 548497 54 are not processed properly (e.g. hyperglycosylation in yeast). In these instances, a different fungal host organism should be selected.

The use of suitable host cells - such as yeast, fungal and plant host cells - may provide 5 for post-translational modifications (e.g. myristoylation, glycosylation, truncation, lapidation and tyrosine, serine or threonine phosphorylation) as may be needed to confer optimal biological activity on recombinant expression products of the present invention.

The host cell may be a protease deficient or protease minus strain.

The genotype of the host cell may be modified to improve expression.

Examples of host cell modifications include protease deficiency, supplementation of 15 rare tRNA's, and modification of the reductive potential in the cytoplasm to enhance disulphide bond formation.

For example, the host cell E. coli may overexpress rare tRNA's to improve expression of heterologous proteins as exemplified/described in Kane (Curr Opin Biotechnol 20 (1995), 6, 494-500 "Effects of rare codon clusters on high-level expression of heterologous proteins in E.coli"). The host cell may be deficient in a number of reducing enzymes thus favouring formation of stable disulphide bonds as exemplified/described in Bessette (Proc Natl Acad Sci USA (1999), 96,13703-13708 " Efficient folding of proteins with multiple disulphide bonds in the Escherichia coli 25 cytoplasm").

ORGANISM The term "organism" in relation to the present invention includes any organism that could 30 comprise the nucleotide sequence coding for the enzyme according to the present invention and/or products obtained therefrom, and/or wherein a promoter can allow 548497 55 expression of the nucleotide sequence according to the present invention when present in the organism.

Suitable organisms may include a prokaryote, fungus, yeast or a plant.

The term "transgenic organism" in relation to the present invention includes any organism that comprises the nucleotide sequence coding for the enzyme according to the present invention and/or the products obtained therefrom, and/or wherein a promoter can allow expression of the nucleotide sequence according to the present invention within the 10 organism. Preferably the nucleotide sequence is incorporated in the genome of the organism.

The term "transgenic organism" does not cover native nucleotide coding sequences in their natural environment when they are under the control of their native promoter which 15 is also in its natural environment.

Therefore, the transgenic organism of the present invention includes an organism comprising any one of, or combinations of, the nucleotide sequence coding for the enzyme according to the present invention, constructs according to the present invention, 20 vectors according to the present invention, plasmids according to the present invention, cells according to the present invention, tissues according to the present invention, or the products thereof.

For example the transgenic organism may also comprise the nucleotide sequence coding 25 for the enzyme of the present invention under the control of a heterologous promoter.

TRANSFORMATION OF HOST CELLS/ORGANISM As indicated earlier, the host organism can be a prokaryotic or a eukaryotic organism. 30 Examples of suitable prokaryotic hosts include E. coli and Bacillus subtilis. 548497 56 Teachings on the transformation of prokaryotic hosts is well documented in the art, for example see Sambrook et al (Molecular Cloning: A Laboratory Manual, 2nd edition, 1989, Cold Spring Harbor Laboratory Press). If a prokaryotic host is used then the nucleotide sequence may need to be suitably modified before transformation - such as 5 by removal of introns.

Filamentous fungi cells may be transformed using various methods known in the art -such as a process involving protoplast formation and transformation of the protoplasts followed by regeneration of the cell wall in a manner known. The use of Aspergillus 10 as a host microorganism is described in EP 0 238 023.

Another host organism can be a plant. A review of the general techniques used for transforming plants may be found in articles by Potrykus (Annu Rev Plant Physiol Plant Mol Biol [1991] 42:205-225) and Christou (Agro-Food-Industry Hi-Tech 15 March/April 1994 17-27). Further teachings on plant transformation may be found in EP-A-0449375.

General teachings on the transformation of fungi, yeasts and plants are presented in following sections.

TRANSFORMED FUNGUS A host organism may be a fungus - such as a filamentous fungus. Examples of suitable such hosts include any member belonging to the genera Thermomyces, Acremonium, 25 Aspergillus, Penicillium, Mucor, Neurospora, Trichoderma and the like.

Teachings on transforming filamentous fungi are reviewed in US-A-5741665 which states that standard techniques for transformation of filamentous fungi and culturing the fungi axe well known in the art. An extensive review of techniques as applied to N 30 crassa is found, for example in Davis and de Serres, Methods Enzymol (1971) 17A: 79-143. 548497 57 Further teachings on transforming filamentous fungi are reviewed in US-A-5674707.

In one aspect, the host organism can be of the genus Aspergillus, such as Aspergillus 5 niger.

A transgenic Aspergillus according to the present invention can also be prepared by following, for example, the teachings of Turner G. 1994 (Vectors for genetic manipulation. In: Martinelli S.D., Kinghorn J.R.( Editors) Aspergillus: 50 years on. 10 Progress in industrial microbiology vol 29. Elsevier Amsterdam 1994. pp. 641-666).

Gene expression in filamentous fungi has been reviewed in Punt et al. (2002) Trends Biotechnol 2002 May;20(5):200-6, Archer & Peberdy Crit Rev Biotechnol (1997) 17(4):273-306.

TRANSFORMED YEAST In another embodiment, the transgenic organism can be a yeast.

A review of the principles of heterologous gene expression in yeast are provided in, for example, Methods Mol Biol (1995), 49:341-54, and Curr Opin Biotechnol (1997) 0ct;8(5):554-60 In this regard, yeast - such as the species Saccharomyces cerevisiae or Pichia pastoris 25 (see FEMS Microbiol Rev (2000 24(l):45-66), may be used as a vehicle for heterologous gene expression.

A review of the principles of heterologous gene expression in Saccharomyces cerevisiae and secretion of gene products is given by E Hinchcliffe E Kenny (1993, "Yeast as a 30 vehicle for the expression of heterologous genes", Yeasts, Vol 5, Anthony H Rose and J Stuart Harrison, Eds., 2nd edition, Academic Press Ltd.). 548497 58 For the transformation of yeast, several transformation protocols have been developed. For example, a transgenic Saccharomyces according to the present invention can be prepared by following the teachings of IHnnen et al.5 (1978, Proceedings of the National Academy of Sciences of the USA 75, 1929); Beggs, J D (1978, Nature, London, 275, 5 104); and Ito, H et al (1983, J Bacteriology 153,163-168).

The transformed yeast cells may be selected using various selective markers - such as auxotrophic markers dominant antibiotic resistance markers.

TRANSFORMED PLANTS/PLANT CELLS A host organism suitable for the present invention may be a plant. A review of the general techniques may be found in articles by Potrykus (Annu Rev Plant Physiol Plant 15 Mo I Biol [1991] 42:205-225) and Christou (Agro-Food-Industry Hi-Tech March/April 1994 17-27).

CULTURING AND PRODUCTION Host cells transformed with the nucleotide sequence of the present invention may be cultured under conditions conducive to the production of the encoded enzyme and which facilitate recovery of the enzyme from the cells and/or culture medium.

The medium used to cultivate the cells may be any conventional medium suitable for growing the host cell in questions and obtaining expression of the enzyme.

The protein produced by a recombinant cell may be displayed on the surface of the cell. 548497 59 The enzyme may be secreted from the host cells and may conveniently be recovered from the culture medium using well-known procedures.

SECRETION Often, it is desirable for the enzyme to be secreted from the expression host into the culture medium from where the enzyme may be more easily recovered. According to the present invention, the secretion leader sequence may be selected on the basis of the desired expression host. Hybrid signal sequences may also be used with the context of 10 the present invention.

Typical examples of heterologous secretion leader sequences are those originating from the fungal amyloglucosidase (AG) gene (gkiA - both 18 and 24 amino acid versions e.g. from Aspergillus), the a-factor gene (yeasts e.g. Saccharomyces, 15 KJuyveromyces and Hansenula) or the ra-amylasc gene (Bacillus).

By way of example, the secretion of heterologous proteins in E. coli is reviewed in Methods Enzymol (1990) 182:132-43.

DETECTION A variety of protocols for detecting and measuring the expression of the amino acid sequence are known in the art. Examples include enzyme-linked immunosorbent 25 assay (ELISA), radioimmunoassay (R1A) and fluorescent activated cell sorting (FACS).

A wide variety of labels and conjugation techniques are known by those skilled in the art and can be used in various nucleic and amino acid assays. 548497 60 A number of companies such as Pharmacia Biotech (Piscataway, NJ), Promega (Madison, WI), and US Biochemical Corp (Cleveland, OH) supply commercial kits and protocols for these procedures.

Suitable reporter molecules or labels include those radionuclides, enzymes, fluorescent, chemiluminescent, or chromogenic agents as well as substrates, cofactors, inhibitors, magnetic particles and the like. Patents teaching the use of such labels include US-A-3,817,837; US-A-3,850,752; US-A-3,939,350; US-A-3,996,345; US-A-4,277,437; US-A-4,275,149 and US-A-4,366,241. 0 Also, recombinant immunoglobulins may be produced as shown in US-A-4,816,567.

FUSION PROTEINS The amino acid sequence for use according to the present invention may be produced as a fusion protein, for example to aid in extraction and purification. Examples of fusion protein partners include glutathione-S-transferase (GST), 6xHis, GAL4 (DNA binding and/or transcriptional activation domains) and (|3-galactosidase). It may also 20 be convenient to include a proteolytic cleavage site between the fusion protein partner and the protein sequence of interest to allow removal of fusion protein sequences.

Preferably, the fusion protein will not hinder the activity of the protein sequence.

Gene fusion expression systems in E. coli have been reviewed in Curr Opin Biotechnol (1995) 6(5):501-6.

In another embodiment of the invention, the amino acid sequence may be ligated to a heterologous sequence to encode a fusion protein. For example, for screening of 30 peptide libraries for agents capable of affecting the substance activity, it may be useful to encode a chimeric substance expressing a heterologous epitope that is recognised by a commercially available antibody. 548497 61 LARGE SCALE APPLICATION In one preferred embodiment of the present invention, the amino acid sequence is used 5 for large scale applications.

Preferably the amino acid sequence is produced in a quantity of from Ig per litre to about 2g per litre of the total cell culture volume after cultivation of the host organism.

Preferably the amino acid sequence is produced in a quantity of from lOOmg per litre to about 900mg per litre of the total cell culture volume after cultivation of the host organism.

Preferably the amino acid sequence is produced in a quantity of from 250mg per litre 15 to about 500mg per litre of the total cell culture volume after cultivation of the host organism.

FOOD The composition of the present invention may be used as - or in the preparation of - a food. Here, the term "food" is used in a broad sense - and covers food for humans as well as food for animals (i.e. a feed). In a preferred aspect, the food is for human consumption.

The food may be in the form of a solution or as a solid - depending on the use and/or the mode of application and/or the mode of administration.

FOOD INGREDIENT The composition of the present invention may be used as a food ingredient. 548497 62 As used herein the term "food ingredient" includes a formulation, which is or can be added to functional foods or foodstuffs and includes formulations which can be used at low levels in a wide variety of products that require, for example, acidifying or emulsifying.

The food ingredient may be in the form of a solution or as a solid - depending on the use and/or the mode of application and/or the mode of administration.

FOOD PRODUCTS The composition of the present invention can be used in the preparation of food products such as one or more of: confectionery products, dairy products, poultry products, fish products and bakery products.

The present invention also provides a method of preparing a food or a food ingredient, the method comprising admixing a lipolytic enzyme according to 1h.e present invention with another food ingredient.

EXAMPLES The present invention will now be described, by way of example only, in which reference may be made to the following figures: Figure 1 shows profiles of lipase activity (indicated by hatched areas, marked as pool B) and protein (broken line) obtained after IEC chromatography.

Figure 2 shows purified fungal lipolytic enzyme, (lane 3-5) applied to a gel (NU-PAGE, 4-12%, Mes-buffer, prepared as described by the manufacturer, Novex, USA), which was then commassie stained.

Figure 3 shows chromatogram #61. 548497 63 Figure 4 shows SDS-PAGE of fractions from the Butyl Sepharose column (P: Pool #172-174 lOOU/mL diluted 1:10; Std = standard protein series).

Figure 5 shows mini baking experiments with 1) Chr #61 frac. 9. 2) Pool #172-# 174. 5 3) Chr. #61 frac. 14. 4) Control. 5) Lipase #3044.

Figure 6 shows GLC analysis of dough lipids digalactosyldiglyceride (DGDG) and digalactosylmonoglyceride (DGMG) from BS8948-2 Figure 7 shows alignment of amino acid sequences of all CBS peptides to the lipase of the Japanese strain of F. heterosporum (Nagao et al. 1994). Identical and similar (well-conserved) amino acids are marked below the alignment with * and ■, respectively.

Figure 8 shows a nucleotide sequence and translated amino acid sequence of the 15 synthetic F. heterosporum (CBS 782.83) lipolytic enzyme gene fused to the synthetic alpha-signal sequence. The amino acid sequence is presented above the nucleotide sequence. The nucleotides containing the restriction enzyme sites Eco RI and Bam HI are underlined and the translational start and stop codons are double underlined. An arrowhead marks the position of the fusion between the alpha-signal sequence and the 20 lipolytic enzyme gene. Arrows indicate the primers used for the assembly of the gene.

Figure 9 shows a schematic representation of the Hansenula expression vector pB14 containing the synthetic F. heterosporum (CBS 782.83) lipolytic enzyme gene (LIPASE) fused to a synthetic alpha-signal sequence (alpha ss). URA3, orotidine-5'-25 phosphate-decarboxylase gene for uracil complementation for selection in Hansenula. HARS. Autonomously replicating sequence for replication in Hansenula. FMD-P, FMD promoter for expression in Hansenula.

Figure 10 shows phospholipase activity of selected Hansenula polymorpha clones 30 containing the synthetic F. heterosporum lipolytic enzyme gene. Lecithin was used as substrate and the free fatty acid was determined using the NEFA kit (Roche). 548497 64 Figure 11 shows a minibread baked with increased dosage(PLU) of phospholipase sample 205 and Lipopan F™.

Figure 12 shows GLC analysis of dough lipids. DGDG^ digalactosyldiglyceride. 5 DGMG digalactosylmonoglyceride. Sum= DGDG+DGMG (Example 3).

Figure 13 shows a HPTLC chromatogram of A) References: 1. Fractionated flour lipid, 2. Hydrolyzed DGDG, 3. DGDG. B) Lipids extracted from dough: 4. Control, 5. 2000 PLU-7/kg sample 205, and 6. 40 ppm Lipopan F™.

Figure 14 shows GLC analysis of isomer digalactosyl- monoglyceride in dough treated with a lipolytic enzyme derived from Fusarium heterosporum.

Figure 15 shows activity of lipolytic enzyme derived from Fusarium heterosporum 15 determined by 10 minutes of enzymation on lecithin substrate, pH 7.0, at various temperatures and subsequent determination of free fatty acids by the NEFA C method.

Figure 16 shows activity of lipolytic enzyme derived from Fusarium heterosporum determined after 30 minutes of incubation in 50 mM phosphate buffer at 3 TIPU/ml 20 and various temperatures (50 mM phosphate buffer, pH 7.0) by 10 minutes of enzymation on lecithin substrate (without CaCL) at 37°C and pH 7.0 and subsequent determination of free fatty acids by the NEFA C method.

Figure 17 shows activity of lipolytic enzyme derived from Fusarium heterosporum 25 determined after 10 minutes of enzymation on lecithin substrate (without CaCli) at 37°C and various pH (50 mM phosphate buffer) and subsequent determination of free fatty acids by the NEFA C method.

Figure 18 shows activity of lipolytic enzyme derived from Fusarium heterosporum 30 determined after 30 minutes of incubation in 50 mM phosphate buffer at 3 TIPU/ml and various pH (50 mM phosphate buffer) by 10 minutes of enzymation on lecithin 548497 65 substrate (without CaCl2) at 37°C and pH 7.0 and subsequent determination of free fatty acids by the NEFA C method.

Figures 19a and 19b show the determination of the molecular weight, as determined by 5 SDS-PAGE, of a lipolytic enzyme derived from Fusarium heterosporum Figure 20 depicts the temperature optimum for a lipolytic enzyme according to the present invention. The enzyme reaction was carried out at various temperatures.

Figure 21 depicts the amount of lecithin in enzyme-modified egg yolk as a function of reaction time at A: 30°C, B: 40°C, and C: 50°C. The amount of lecithin was analysed by LC/MS-MS and is expressed as percentage of egg yolk.

Figure 22 depicts the amount of lyso-lecithin in enzyme-modified egg yolk as a 15 function or reaction time at A: 30°C, B: 40°C, and C: 50°C. The amount of lysolecithin was analysed by LC/MS-MS and is expressed as percentage of egg yolk.

Figure 23 depicts the amount of free fatty acid in enzyme modified egg yolk as a function of reaction time at A: 30°C, B: 40°C, and C: 50°C. The amount of free fatty 20 acid was analysed by the NEFA C method and is expressed as percentage of egg yolk.

Figure 24 depicts the enzymatic conversion of egg yolk with a lipolytic enzyme according to the present invention (Example 4). The amounts of lyso-lecithin (A), free fatty acid (B), and lecithin (C) as a function of reaction time. The error bars indicate 25 the standard deviation of the double determinations (n=2). The amount of lecithin and lysolecithin were determined by LC/MS-MS and the amount of free fatty acid was determined by the NEFA C method. Results are expressed as percentage of egg yolk.

Figure 25 depicts the enzymatic conversion, of egg yolk with Lecitase® Ultra 30 phospholipase from Novozymes A/S (Example 4). The amounts of lyso-lecithin (A), free fatty acid (B), and lecithin (C) as a function of reaction time. The error bars indicate the standard deviation of the double determinations (n=2). The amount of 548497 66 lecithin and lysolecithin were determined by LC/MS-MS and the amount of free fatty acid was determined by the NEFA C method. Results are expressed as percentage of egg yolk.

Figure 26 shows TLC analysis (the solvent was chloroform:methanol:water (65:24:4)) of lipid extract from modified egg yolk (Example 4). 1:PC and LPC standard. 2: Lipolytic enzyme according to the present invention, 10°C, 240 min. 3: Lipolytic enzyme according to the present invention, 20°C, 240 min. 4: Lipolytic enzyme according to the present invention, 53 °C, 240 min. 5: Lipolytic enzyme according to 10 the present invention, 20°C, 1440 min. 6: Lecitase® Ultra, 10°C, 4h. 7: Lecitase® Ultra, 20°C, 240 min. 8: Lecitase® Ultra, 53°C, 4h. 9: Lecitase® Ultra, 20°C, 1440 min. 10: Control sample. The compounds listed to the left of the TLC plate are cholesterol (C)5 triacylglyceride (TG), diacylglyceride (DG), free fatty acid (FFA), monoacylglyceride (MG), phosphatidylethanoiamme (PE), phosphatidylcholine (PC), 15 lyso-pbosphatidy lethanolamine (LPE), and lyso-phosphatidylcholine (LPC).

Figure 27 depicts the relation between change in lyso-lecithin and free fatty acid content during enzymation of egg yolk with a lipolytic enzyme according to the present invention and Lecitase® Ultra phospholipases, respectively (Example 4). The 20 results are based on a molar weight of lyso-lecithin of 523 and a molar weight of free fatty acids of283. Free fatty acid was determined by the NEFA C method, lysolecithin and lecithin was determined by LC/MS-MS.

Figure 28 shows HPTLC analysis (the solvent was p-ether:MTBE:acetic acid 25 (50:50:1)) of lipid extract from modified egg yolk (Example 4). The compounds listed to the left of the TLC plate are triacylglyceride (TG), free fatty acid (FFA), 1,3 diacylglyceride (1,3 DG); 1,2 diacylglyceride (1,2 DG),cholesterol (C), monoacylglyceride (MG), phosphatidylethanolamine (PE), phosphatidylcholine (PC), lyso-phosphatidylethanolamine (LPE), and lyso-phosphatidylcholine (LPC).

Figure 29 shows TLC analysis (solvent IV) of mayonnaise made with enzyme-modified egg yolk from Srnofa A/S (Example 5). 548497 67 Figure 30 shows mayonnaise prepared from enzyme-modified egg yolk from Sanofa A/S heat-treated in a microwave oven (Example 5). Sample 1 was a control with water added instead of enzyme solution, sample 2 contained 30 U/g lipolytic enzyme 5 according to the present invention, and sample 3 contained 30 U/g Lecitase® Ultra.

Figure 31 shows the specific bread volume of hard crusty rolls baked with different concentrations of a lipolytic enzyme according to the present invention alone or in combination with Panodan® M2020 DATEM emulsifier and tested against a 10 combination of Lipopan F™ and DATEM as well as pure Lipopan F™ or pure DATEM.

Figure 32 shows'the specific bread volume of hard crusty rolls baked with different concentrations of a lipolytic enzyme according to the present invention alone or in 15 combination with Panodan® A2020 DATEM or SSL P 55 emulsifier and tested against a combination of Lipopan F™/SSL P 55 or Lipopan™/DATEM as well as pure Lipopan F. pure DATEM and pure SSL P 55.

Figure 33 shows nucleotide sequence (SEQ ID No, 5) and deduced amino acid 20 sequence (SEQ ID No.4) of the F. semitectum (IBT 9507) lipase cDNA. The deduced amino acid sequence is presented above the nucleotide sequence. Arrows indicate the primers used for the amplification of the cDNA.

Figure 34 shows a schematic representation of the Hansenula expression vector 25 pDB14-alp-sem containing the F. semitectum lipase gene (Lipase) fused to the a-signal sequence (alpha ss.). AP(R), URA3, orotidine-5' phosphate-decarboxylase gene for uracil complementation for selection. HARS, Autonomously replicating sequence for replication in Hansenula. FMD-P, FMD promoter for expression in Hansenula.

Figure 35 shows phospholipase activity of a lipolytic enzyme from Fusarium semitectum IBT9507 as a function of temperature. 548497 68 Figure 36 shows phospholipase activity of a lipolytic enzyme from Fusarium semitectum IBT9507 as a function of pH.

Figure 37 shows an amino acid sequence (SEQ ID No. 1) of a fungal lipolytic enzyme 5 derived from Fusarium heterosporum.

Figure 38 shows an amino acid sequence of a fungal lipolytic enzyme derived from Fusarium heterosporum comprising an N terminal signal sequence (underlined) (SEQ ID No. 2).

Figure 39 shows a nucleotide sequence (SEQ ID No. 3) encoding a fungal lipolytic enzyme derived from Fusarium heterosporum in accordance with the present invention.

Figure 40 shows an amino acid sequence (SEQ ID No. 4) of a lipolytic enzyme derived from Fusarium semitectum.

Figure 41 shows a nucleotide sequence (SEQ ID NO. 5) encoding a lipolytic enzyme derived from Fusarium semitectum.

Figure 42 shows an amino acid sequence (SEQ ID No.6) of a lipolytic enzyme derived from Fusarium heterosporum (EAEA is a pro-peptide originally from the a-factor signal sequence).

Figure 43 shows a nucleotide sequence (SEQ ID No.7) of a lipolytic enzyme derived from Fusarium heterosporum which includes a a-factor signal sequence.

Example 1. Expression, purification, sequencing and baking trials of a Fusarium heterosporum lipolytic enzyme. 548497 69 FERMENTATION Fusarium heterosporum CBS 782.83 strain was obtained from Centraalbureau voor Schimmelcultures (the Netherlands).

Growth media Glucose-yeast extract agar Yeast extract 4g/L KH2P04 1 g/L MgS04,7H20 0.5 g/L Glucose 15 g/L Agar 20 g/L Glucose was added after autoclaving 1.4 Pre-fermentation medium Soy flour 50 g/L Glucose monohydrate 50 g/L KH2P04 2 g/L Na2HP04 3 g/L Soy oil 1 g/L The medium was prepared in 500 mL shake flasks with baffles and 100 mL was added pr shake flask. The soy oil was added to each flask separately.

Glucose was added after autoclaving.

Production medium Peptone 10 g/L Tween TM-80 12 g/L MgS04, 7H20 2 g/L CaCI2, 2H20 0.1 g/L The medium was prepared in 500 mL shake flasks with baffles and 100 mL was added pr shake flask. The Tween TM-80 was added to each flask separately. 548497 70 pH was adjusted to 6.0 before autoclaving.

Culture conditions Fusarium heterosporum CBS 782.83 was inoculated on glucose-yeast extract agar 5 plates, which were incubated at 24°C until development of spores.

A shake flask containing pre-fermentation medium was inoculated with 4 cm2 of agar plate containing a well sporulating culture. The shake flask was incubated at 30°C and 200 RPM. After three days of growth, 30 production medium shake flasks were each inoculated with 5 mL fermentation broth from the pre-fermentation shake flask. The 10 production medium shake flasks were incubated at 30°C and 200 RPM.

Ten production medium shake flasks were harvested after 2,3 and 4 days of growth. The biomass was removed by centrifugation followed by sterile filtration of the supernatant through 0.2 jam filters (VacuCap 90 Filter Unit w/0.2 (am Supor Membrane) from Gelman Laboratory. After filtration, the filtrate was frozen at -80 °C 15 and stored until analysis.

ANALYTICAL PROCEDURES Phospholipase activity was determined according to the "PLU assay" previously 20 described herein.

APPLICATION TLC analysis TLC-plate was activated in a heat cupboard (110 °C) for Vi h. 100 mL running buffer was poured into a chromatography chamber with lid. The walls of the chamber were covered with filter paper (Whatman 2) in order to saturate the chamber with the solvent vapor.

The TLC-plate was placed in a frame and the sample was applied onto the TLC plate 2 30 cm from the bottom. The TLC plate was then placed in the TLC chamber with the chosen running buffer. When the running buffer reached 14 cm from the bottom of the 548497 71 plate, the TLC plate was taken out and dried in fume board, and then placed in the heat cupboard at 110°C for 10 minutes.

The TLC-plate was then immersed in the developing reagent, and dried in the heat cupboard at 110° C for 15 minutes Running-buffer: Nr. IV: Chloroform : Methanol: H20 ( 65:25:4) Nr. I : P-ether : methyl-tert-butyl ether (MTBE): Acetic acid (60:40:1) Developing buffer (Vanadate-buffer): 32 g Na2C03 ad 300 mL H20 (1M) 18.2 g vanadate pentoxide (V205) was added and dissolved during gentle heating and baked in a "BACO-LINE" oven for 6 minutes.

The solution was cooled to ambient.

Carefully 460 mL 2.5 M H2SO4. (460 mL H20 + 61 mL H1SO4) is added Water was added to 1000 mL.

Gas Chromatography Perkin Elmer 8420 Capillary Gas Chromatography equipped with WCOT fused silica 20 column 12.5 m x 0.25 mm ID x 0.1 jim 5%phenyl-methyl-silicone (CP Sil 8 CB from Crompack).

Carrier: Helium.

Injection: 1.5 |xL with split.

Detector: FID. 385 °C.

Oven program: 1 2 3 4 Oven temperature [°C] 80 200 240 360 Isothermal, time [min] 2 0 0 Temperature rate [°C/min] 12 Sample preparation: 50 mg wheat lipid was dissolved in 12 mL heptane: pyridine 2:1 containing an internal standard heptadecane, 2 mg/mL. 500 p.L of the sample was 548497 72 transferred to a crimp vial. 100 pL MSTFA (N-Methyl-N-trimethylsilyl-trifluoraeetamid) was added and the reaction incubated for 15 minutes at 90°C. Calculation: Response factors for mono-di-triglycerides, free fatty acid and galactolipids were determined from reference mixtures of these components. Based on 5 these response factors the lipids in the dough were calculated.

Mini Baking Test.

The following ingredients were added to a 50 g Brabrender mixing bowl and kneaded for 5 minutes at 30°C: flour 50 g, dry yeast 10 g, sugar 0.8 g, salt 0.8 g, 70 ppm 10 ascorbic acid and water (to a dough consistency of 400 Brabender units). Resting time was 10 min. at 34 °C. The dough was scaled 15 g per dough. Then molded on a special device where the dough was rolled between a wooden plate and a Plexiglas frame. The doughs were proofed in tins for 45 min. at 34 °C, and baked in a Voss household oven for 8 min. 225 °C.

After baking the breads were cooled to ambient temperature and after 20 min. The breads were scaled and the volume was determined by rape-seed displacement method. The breads were also cut and crumb and crust evaluated.

Pilot Baking tests (Hard Crust Rolls) Flour, Danish reform 1500 gs Compressed Yeast 90 g, sugar 24 g, salt 24 g. water 400 Brabender units + 2% were kneaded in a Hobart mixer with hook for 2 minutes at low speed and 9 minutes at high speed. The dough temperature was 26°C. The dough was scaled 1350 gram. The dough was rested for 10 minutes at 30°C and molded on a Fortuna molder. The dough was then proved for 45 minutes at 34 °C. The dough was 25 baked in a Bago-oven for 18 minutes at 220°C and steamed for 12 seconds After cooling, the rolls were scaled and the volume of the rolls was measured by the rape seed displacement method.

Specific bread volume Specific volume - Volume of the bread, ml 3 0 weight of the bread, gram 548497 73 RESULTS AND DICUSSION Fermentation The fermentation samples were analyzed for phospholipase activity, and the results are 5 shown in Table 1.

Table 1 Results of fermentation 1 ID Organism Sample label PLU-7 f 172 1 Fusarium heterosporum CBS 782.83 aMedium D. day 2 j 173 Fusarium heterosporum CBS 782.83 Medium D. day 3 33 j 174 Fusarium heterosporum CBS 782.83 Medium D. day 4 26 aMedium D = production medium It was seen that the phospholipase activity was almost identical at days 2, 3 and 4, and all samples were therefore pooled and named JBS-2254-97-3.

Purification and sequencing Purification of phospholipase from crude extract using anion exchange chromatography: The column (Q-Sepharose FF, 1.5 X 2.8 cm, 5 mL gel) was prepared as described by 20 the maaufacturer (Amersham Bio.), and then equilibrated in 20 mM tris/HCl buffer, 0.1 M NaCl, pH 7.5 (buffer A). The sample (15 mL) was added 0.1 M NaCl and applied to the column at a flow rate of 3.5 mL/min. The lipolytic enzyme was eluted with a linear gradient of 0-0.6 M NaCl in buffer A (See Figure 1). Fractions of 3.5 mL were collected during the entire run. 10 pL of each fraction were subjected to spot 25 plate assay. Lipase activity was determined by tributyrin and lecithin spot plate assay (10 (iL of each fraction were transferred to the hole and the plate was incubated at 40°C. Formation of haloes in the agarose gels takes place as a function of time. A 548497 74 blank without enzyme was also added to one of the holes for comparison). The fractions containing lipolytic activity was then subjected to SDS-PAGE (See Figure 2) and N-terminal analyses.

Enzymatic fingerprinting by MALDI-TOF and amino acid sequencing The protein was reduced with Dithiothreitol and the cysteine residues were protected by carboxymethylation using iodoacetamide. The protein was cleaved by trypsin and the fragmentation pattern of the tryptic peptides were examined by MALDI-TOF 10 analysis. The peptides were separated by chromatography on a Cis - reverse-phase HPLC column, and the degree of purification was monitored by MALDI-TOF analysis. The amino acid sequence was determined by Edman degradation as previously described in details in TR6452.

The entire amino acid sequence of Fusarium heterosporum lipolytic enzyme has been determined. The digestion with trypsin gave very specific peptides where the MW (MALDI-TOF) could be determined conclusively. The amino acid sequences for all the peptides were also determined by Edman degradation. The amino acid sequence determined by Edman degradation covers 99.64% of the polypeptides chain of the F. 20 heterosporum lipolytic enzyme.

Summary of the MALDI-TOF and Edman degradation studies is shown in Table 2.

Table 2 Enzymatic fingerprinting and MW of the tryptic peptides from the Fusarium heterosporum lipolytic enzyme, and determination of the 25 entire amino acid sequence by Edman degradation.

Fusarium heterosporum Lipolytic enzyme (2254-97-3) nr From Sequence M+H calc M+H obs 548497 75 1 1-13 AVGVTSTDFTNFK 1387.5 2+ 14-33 F YIQHGAAA Y CNSGTAAGAK 2059.2 2059. 0 3+ 34-59 ITCSNNGCPTIESNGVTVVASFTGSK 2701.9 4+ 60-72 TGIGGYVSTDSSR 1300.4 + 73-73 K 147.2 6+ 74-80 EIVVAIR 780.0 780.0 7 81-86 GSSNIR 632.7 8+ 87-128 NWLTNLDFDQSDCSLVSGCGVHSGFQNAWA EISAQASAAVAK 4514.8 9 129-130 AR 246-3 131-131 K 147.2 11 132-137 ANPSFK 663.8 12+ 138-158 VVATGHSLGGAVATLSAANLR 1966.3 1966. 1 13+ 159-173 AAGTP VDIYTY GAPR 1552.7 1552. 6 14+ 174-192 VGNAALSAFISNQAGGEFR 1910.1 1910. 0 193-197 VTHDK 599.7 16 198-202 DPVPR 583.7 17+ 203-211 LPPLIFGYR . 1076.3 1076. 3 18+ 212-226 HTTPEYWLSGGGGDK 1605.7 19+ 227-235 VDYAISDVK 1010.1 20a 236-274 VCEGAANLMCNGGTLGLDIDAHLHYFQATD ACNAGGFSW* 4231.5 4233. 2 20b+ 236-275 VCEGAANLMCNGGTLGLDIDAHLHYFQATD ACNAGGFSW*R 4387.7 4387. 8 + = Confirmed by Edman sequencing * = oxidised Tryptophan Sequence coverage = 99.64% 548497 76 The complete amino acid sequence of Fusarium heterosporum lipolytic enzyme is shown as SEQ ID No. 1 (see Figure 37).

Application trials A pool of 2 litres from the three samples of F. heterosporum (Table 1), labeled Pool #172-174, was concentrated by ultrafiltration (10 kDa filter) on an Amicon Ultra Filtration unit. 250 ml of the retentate contained approx. 100 PLU-7/ml. The retentate was adjusted to 1 M Ammonium-acetate and applied onto a 27 ml Butyl Sepharose 10 column (2.5 cm id.) and eluted with A-buffer 1M NELracetate in 20 mM TEA pH 7.4 and B-buffer 20 mM TEA pH 7.4. The chromatogram (#61) from the purification is shown in Figure 3.

Fractions from the chromatogram #61 were analyzed by SDS-PAGE as shown in 15 Figure 4. mL fractions from this chromatography were collected and analyzed for phospholipase activity as shown in Table 3. These results indicate a quite high amount of phospholipase activity in the fractions eluted in the main peak of the chromatogram. 20 Small amount of activity is not bound to the column but is eluted in the front. Although the SDS gel did not run so nicely, it is observed that the fractions contain several proteins but fraction 14 and 15 contain one main band, which is expected to be the fungal lipolytic enzyme.

Table 3 Chromatogram #61.

PLU-7 Frac. 8 32 Frac. 9 89 Frac. 10 69 Frac. 11 51 548497 77 Frac. 12 39 Frac. 13 81 Frac. 14 23 Frac. 15 17 Fraction 9 and fraction 14 from chromatogram #61 were used for a mini baking test and also the non-purified pool #172-174 was tested in mini baking test. Results from 5 this baking experiment are shown in Table 4. This clearly shows that purified lipolytic enzyme from F. heterosporum CBS 7S2.83 gives very good baking results in term of improved bread volume. Also the non-purified sample contributed to a very nice bread volume. The crumb structure of the breads were also improved very much by F. heterosporum lipolytic enzyme as indicated in Figure 5 and evaluated better than a 10 lipase from Pseudomonas cepacia #3044.

Table 4 Sample Enzyme PLU-7/50 g flour Bread volume, mL/g 1 Chr #61 frac 9 100 U 4.33 2 Pool #172-174 100 U 4.33 3 Chr #61 frac. 14 100 U 4.60 4 Control 0 3.29 Lipase, #3044 40ppm 4.38 Dough from this mini-baking experiment were extracted with water-saturated-butanol and the lipids were analysed by TLC. TLC analysis confirmed that Lipase #3044 is more active on triglyceride than the lipolytic enzyme from F. heterosporum samples. The amount of free fatty acids (FFA), are also higher with lipase #3044. TLC in solvent IV indicates a component (DGMG), which is clearly higher in the samples of 20 dough lipids treated with F. heterosporum compared with a triglyceride hydrolysing lipase #3044. 548497 78 The purified fractious from F. heterosporum were also tested in pilot baking experiment with the results shown in Table 5.

Table 5 Use of purified chromatography fractions from Fusarium heterosporum in pilot baking test and effects on bread volume.

No.

Specific volume (ccm/g) 1 Control .11 2 500UF. het. Pool #172-#174 6.28 3 1000U F. het Pool #172-#174 6.79 4 40ppm #3044 (Pseudomonas) .27 2000U F. het Pool #172-#174 6.24 6 4000U F. het. Pool #172-#174 4.95 7 1000U 2254-97 C61 6.95 8 40 ppm#3016 (LipopanFIM) 6.97 Dough from this baking test were extracted with water-saturated-butanol and the 10 dough lipids analyzed by GLC analysis with results shown in Table 6.

Table 6 GLC analysis of dough lipids. GL=glycerol. FFA~ free fatty acid. MGMG=monogalactosylmonoglyceride. DAG- Diglyceride. DGMG digalactosylmonoglyceri.de. MGDG= monogalactosyldiglyceride.

DGD G=digalacto syldigly ceri de. TRI- triglyceride.

GL FFA MGMG DAG DGMGMGDG DGDG TRI Control 0.120 0.152 0.0015 0.0771 0.0195 0.0644 0.172 0.770 500U F. het. Pool #172-#174 0.121 0.250 0.012 0.059 0.057 0.030 0.139 0.792 1000U F. het Pool #172-# 174 0.121 0.277 0.018 0.056 0.087 0.010 0.102 0.738 WO 2005/087918 PCT/IB2005/000875 79 40ppm #3044 0.127 0.368 0.002 0.132 0.022 0.066 0.173 0.276 2000U F. het. Pool #172-#174 0.122 0.320 0.018 0.060 0.119 0.013 0.062 0.723 4000U F. het. Pool #172-#174 0.128 0.332 0.021 0.065 0.146 0.010 0.033 0.739 1000U 2254-97 C61 0.125 0.287 0.019 0.067 0.088 0.016 0.099 0.655 40 ppm#3016 0.124 0.284 0.017 0.058 0.086 0.014 0.101 0.723 dTRI dDGDG dDGDG/dTRI Control 500U F. het. Pool #172-#174 0 0.033 n/a 1000U F. het Pool #172-#174 0.032 0.07 2.19 40ppm #3044 0.494 0 n/a 2000U F. het. Pool #172-# 174 0.047 0.11 2.34 4000U F. het. Pool #172-#174 0.031 0.139 4.4 1000U 2254-97 C61 0.115 0.073 0.63 The ratio of DGDG hydrolysis compared to triglyceride hydrolysis is shown in Table 7.

The GLC analysis of galactolipids, are also illustrated graphically in Figure 6.

The GLC results confirm that the amount of DGMG produced in dough by F. heterosporum is higher than the amount produced by 40 ppm Lipopan F (#3016). The results also indicate a higher degree of hydrolysis of MGDG than DGDG. The results also indicate that the amount of hydrolyzed triglyceride is low compared with a normal triglyceride-hydrolyzing enzyme like #3044 from P. cepacia. The pilot scale baking results and the lipid analysis confirmed that the lipolytic enzyme from F.heterosporum CBS 782-83 has clear hydrolytic activity on digalactosyldiglyceride (DGDG) and the formation of digalactosylmonoglyceride (DGMG) in a dough.

Table 7 Ratio of DGDG hydrolysis compared to triglyceride hydrolysis of purified chromatography fractions from Fusarium heterosporum 548497 80 40 ppm#3016 0.047 0.071 1.5 4. CONCLUSIONS In this study, a fungal lipolytic enzyme from F. heterosporum CBS 782.83 was produced by fermentation in shake flasks. The enzyme was purified and the amino acid sequence was determined. The enzyme has about 83% homology to a commercial lipase from F. oxysporum (LipopanF™). The enzyme gave very good results in baking 10 trial in terms of improved bread volume and improved crumb structure. Lipid analysis from dough confirmed that the enzyme was active on galactolipids during production of galactomonoglycerides. Without any optimization of dosage, the baking results indicate that the a fungal lipolytic enzyme from F. heterosporum CBS 782.83 is at least equivalent to the commercial eri2yme LipopanF, and the comparative DGDG to 15 triglycerides activity indicate that this enzyme has a superior enzymatic activity in a dough environment compared to LipopanF™.

EXAMPLE 2. Construction and expression of a synthetic gene encoding a 20 lipolytic enzyme from Fusarium heterosporum (CBS 782.83) in Hansenula polymorpha.

The amino acid sequence of a fungal lipolytic enzyme isolated from Fusarium heterosporum (CBS 782.83) was determined and used to design and clone a synthetic 25 lipolytic enz3Tne gene for expression in Hansenula polymorpha. To favour high expression, the codons of the synthetic gene were optimised to be in accordance with the codon preferences of Hansenula polymorpha, A codon optimised alpha-factor signal sequence was synthesised as well and cloned in front of the synthetic lipolytic enzyme gene. The assembled construct was transferred into the expression vector 548497 81 pB14 and transformed into Hansenula polymorpha. pB14 is a plasmid without genes conferring antibiotic resistance and can therefore be used in production facilities.

A number of lipolytic enzyme producing Fusarium strains were screened for activities 5 with a high ratio of activity on of galactolipids and/or phospholipids when compared to triglycerides.

Several of the strains have been selected as producing lipolytic enzymes of interest. Among these is the Fusarium heterosporum (CBS 782.83). The lipolytic enzyme from 10 this strain has therefore been isolated and the amino acid sequence has been determined. The amino acid sequence was back translated into a nucleic acid sequence that was used to design and construct a synthetic gene for expression in Hansenula polymorpha.

EXPERIMENTAL The strain of Hansenula used in this study was the uracil-auxotrophic Hansenula polymorpha strain RB11 {odd) obtained from Rhein Biotech GmbH (Diisseldorf, Germany).

Enzymatic fingerprinting by MALDI-TOF and amino acid sequencing.

A protein having lipolytic enzyme activity was isolated from Fusarium heterosporum (CBS 782.83). The protein was reduced with dithiothreitol and the cysteine residues 25 were protected by carboxymethylation using iodoacetamide. The protein was cleaved by trypsin and the fragmentation pattern of the tryptic peptides were examined by MALDI-TOF analysis. The peptides were separated by chromatography on a Cis -reverse-phase HPLC column, and the degree of purification was monitored by MALDI-TOF analysis. The amino acid sequence was determined by Edman 30 degradation as previously described in details in TR6452. 548497 82 Design and construction of a synthetic lipolytic enzyme gene.

The amino acid sequences of the peptide fragments were ordered by alignment with the Japanese strain of F. heterosporum (Nagao et al. 1994). The complete amino acid 5 sequence thus obtained was back translated into a nucleic acid sequence to reveal all possible codons. For each codon the codon most favourable for expression in Hansenula polymorpha was chosen according to the codon preference table of genes expressed in Hansenula polymorpha. Synthetic oligonucleotides, each about 100 nucleotides long, comprising the complete gene, were synthesised, and the gene was 10 assembled by PCR. For the final amplification of the gene was used an upstream primer (alps.cbss) designed with the most 5' nucleotides from the 3'-end of the alpha-factor signal sequence to allow in frame fusion, and a downstream primer (cbss.t) designed with a Bam HI restriction enzyme site for cloning purposes (Table 8).

A nucleotide sequence encoding the signal sequence from the yeast alpha mating factor was similarly synthesised with favourable codons by oligonucleotides and amplified by PCR. For the final amplification of the alpha-signal sequence was used an upstream primer (alpsynt) designed with an Eco RI restriction enzyme site for cloning purposes, and a downstream primer (cbss.alps) designed with the most 5' 20 sequences from the 5'-end of the synthetic lipolytic enzyme gene to allow in frame fusion (Table 8).

To fuse the synthetic alpha-factor signal sequence to the synthetic lipolytic enzyme gene the two fragments were mixed and re-amplified with the outer primers alpsynt 25 and cbss.t (Table 8). The PCR product was cloned into the vector pCR 2.1-TOPO (Invitrogen) and the nucleotide sequence of the inserts were determined using a BigDye Terminator v3.0 cycle sequencing kit (Applied Biosystems) and an ABI Prism 3100 Genetic Analyzer (Applied Biosystems). 548497 83 Gene Primer sequence Restric tion site CBSLip '- alps.cbss '- TCCTTGGAC A A CtACtAGCCGTTGGAGTGACC None TCTACTG 3'-cbss.t '- AGGATCCAATTCTCTCCATGGCCTATCTCCA GGAGAA ACCTCCG Bam HI a-signal '-alpsynt '- AGAATT C AAACGAT GAGATT CC CAT C CAT C TTTACCG Eco RI 3'- '- None cbss.alps AGGTCACTCC A ACGGCTCTCTTGTCC A AGG AAACAC CTTCC Table 8. Primer sequences used for the amplification and assembly of the synthetic F. heterosporum (CBS 782.83) lipolytic enzyme gene and the synthetic alpha-signal sequence. The restriction enzyme sites introduced for cloning purposes in each primer 5 are underlined. The nucleotides included allowing fusion of the synthetic lipolytic enzyme gene and the synthetic alpha-signal are double underlined.

Expression of lipolytic enzyme in Hansenula polymorpha.

To express the synthetic F. heterosporum (CBS 782.93) lipolytic enzyme gene in Hansenula the combined alpha-signal sequence/lipolytic enzyme gene was inserted behind the FMD-promoter into the Hansenula expression vector pB14, a plasmid without genes conferring antibiotic resistance. After conformation of the expected 15 structure of the assembled plasmid in E. coli, the plasmid was transformed into competent Hansenula polymorpha cells by electroporation. Transform ants were 548497 84 selected on YND plates and colonies were further selected for multiple integration of the gene by 3 and 8 passages of 1:200 dilutions in liquid cultures of YND. Finally, the selected cultures were stabilised by transferring twice in YPD medium. To farther select for high expressers each cultures showing high level of expression were plated 5 for single colonies, which each were assayed for expression level.

To determine the level of expression of the lipolytic enzyme gene the selected clones were grown in YPD with 1.8% glycerol and 0.2% glucose for 2 days at 24°C.

Enzyme activity Samples of the culture medium were analysed for lipolytic enzyme activity with Lecithin or DGDG as substrates and using the NEFA Kit (Roche) scaled down to volumes suitable for micro titre plates for determination of the liberated free fatty acids.

RESULTS Enzymatic fingerprinting by MALDI-TOF and amino acid sequencing.

The entire amino acid sequence of Fusarium heterosporum lipolytic enzyme has been determined (See SEQ ID No. 1 - Figure 37). The digestion with trypsin gave very specific peptides where the MW (MALDI-TOF) could be determined conclusively. The amino acid sequences for all the peptides were also determined by Edman degradation. The amino acid sequences determined by Edman degradation covers 25 99.64% of the polypeptide chain of the F. heterosporum (CBS 782.83) lipolytic enzyme. The amino acid sequences of all peptides were aligned to the lipase of the Japanese strain of F. heterosporum (Nagao et al. 1994 J. Biochem. 116: 536-540) thus revealing the order of the peptides identifying the amino acid sequence of the mature protein. The alignment is shown in Figure 7. Summary of the MALDI-TOF and 30 Edman degradation studies is shown in Table 9 with the peptides order according to the alignment with the Nagao sequence. 548497 85 Fusarium heterosporum Phospholipase (2254-97-3) Partial cleavage Nr From Sequence m+h calc m+h obs Peptides m+h calc m+h obs 1 1-13 avgvtstdftnfk 1387.5 2+ 14-33 fyiqhgaaay cnsgtaagak 2059.2 2059 1+2 3427 3427 3+ 34-59 itcsnngcptiesngvtwasftgsk 2701.9 4+ 60-72 tgiggyvstdssr 1300.4 3+4+5 4111 4112 + 73-73 k 147.2 6+ 74-80 eivvair 780.0 780.0 4+5+6 2209 2209 7 81-86 gssnir 632.7 8+ 87-128 nwltnldfdqsdcslvsgcgvhsgfq nawaeisaqasaavak 4514.8 7+8 5129 5129 9 129-130 ar 246.3 8+9 4743 4743 131-131 k 147.2 11 132-137 anpsfk 663.8 12+ 138-158 watgiislggavatlsaanlr 1966.3 1966 +11 +12 2739 2739 13+ 159-173 aagtpvdiytygapr 1552.7 1552 14+ 174-192 vgnaalsafisnqaggefr 1910.1 1910 193-197 vthdk 599.7 16 198-202 dpvpr 583.7 17+ 203- 211 lpplifgyr 1076.3 1076 +16 +17 2221 2221 18+ 212-226 httpeywlsggggdk 1605.7 19+ 227-235 vdyaisdyk 1010.1 18+19 2596 2596 20a 236-274 v cegaanlmcnggtlgldldah lhyfqatdacnaggfsw* 4231.5 4232 20b + 236-275 v cegaanlmcn ggtlgldidahl hyfoatdacnaggfsw*r 4387.7 4387 Table 9. Enzymatic fingerprinting, MW determination of the entire amino acid sequence by Edman degradation of the tryptic peptides from the Fusarium 5 heterosporum (CBS 782.83) lipolytic enzyme. Peptide sequences confirmed by Edman 548497 86 degradation are marked +. Oxidised Tryptophan is marked by *. Sequence coverage = 99.64%.

Identity to other Fusarium lipases Alignments of the amino acid and nucleotide sequence of F. heterosporum (CBS 782.83) lipolytic enzyme with sequences from other Fusarium lipases show the relationships between some of the Fusarium lipases (Table 10).

LIPASE IDENTITIES F. heterosporum (Nagao supra) F. oxysporum (Lipopan F™) F. heterosporum (CBS 782.83) amino acid (SEQ ID No. 1) 58.7% 85.1% F. heterosporum (CBS 782.83) nucleotide sequence (SEQ ID No. 3) 61.8% 69.2% Table 10. Amino acid and nucleotide identity of F. heterosporum (CBS 782.83) lipolytic enzyme compared to other Fusarium lipases.

Mixing and amplification by PCR of the synthetic oligonucleotides for the lipolytic 15 enzyme gene and the alpha-signal sequence resulted in DNA fragments, which were cloned and sequenced. Fragments containing the correct sequences were used to assemble the complete gene by re-amplification using the primers shown in Table 8. The assembled nucleotide sequence is shown in Figure 8 with its translated amino acid sequence, and the primers used are indicated with arrows.

The DNA fragment containing the assembled gene construct was transferred to the Hansenula expression vector pB14 using the introduced restriction enzyme sites. The resulting plasmid pB14-alps.cbss is schematically shown in Figure 9. 548497 87 Expression of fungal lipolytic enzyme activity in selected clones.

The clones, which have been through the selection process, were analysed for 5 expression of lipolytic enzyme. 10-microlitre samples of the supernatant of 2 day cultures were incubated with either DGDG or lecithin for 10 minutes and 10 microlitres of these reactions were analysed with the NEFA kit. The results after single colony isolation of 3 of the clones are shown in Figure 10.

The amino acid sequence of a lipolytic enzyme from a strain of Fusarium heterosporum (CBS 782.83) has been determined and a synthetic gene encoding this lipolytic enzyme has been constructed and optimised for expression in Hansenula polymorpha. The gene that encoded the mature enzyme was fused to a synthetic signal sequence derived from the yeast mating alpha-factor. The combination of the alpha-15 signal sequence with the FMD promoter of the Hansenula pB 14 vector has previously been shown to be suitable for expression of Fusarium lipases.

EXAMPLE 3: Expression of a Fusarium heterosporum CBS 782.83 lipolytic 20 enzyme in Hansenula polymorpha and characterization of the product in baking trials The Hansenula polymorpha strain B14:8-3,8 (DCDK0172), containing a lipolytic enzyme-encoding gene from the filamentous fungus Fusarium heterosporum 25 CBS782.83, was fermented in the fed-batch mode. After 160 hours of fermentation the phospholipase activity reached 1200 U/mL. Based on the fermentations three products were made and tested further. The products are named the following: sample 205, -206 and -209.

A lipolytic enzyme sample 205 from F. heterosporum expressed in H. polymorpha 30 was tested in miniscale baking experiments. Dough from the baking experiment was analyzed by GLC and HPTLC. 548497 88 The baking results from mini scale baking confirm a very strong improvement of lipolytic enzyme sample205 on bread volume and improvement of crumb structure. Lipolytic enzyme analysis confirmed a strong hydrolytic activity of lipolytic enzyme sample 205 on digalactosyldiglyceride(DGDG) concomitant with the accumulation of 5 digalactosylmonoglyceride(DGMG).

The enzyme had only minor activity on triglycerides in the dough.

Samples 206 and 209 were tested in pilot scale baking trials and confirmed the good baking performance of the lipolytic enzymes both with respect to increased bread volume and improved crumb structure. From the baking trials, it is indicated that 10 sample 206 perform a bit better compared to sample 209 in a straight dough procedure, however the two products have not been compared directly to each other and more baking trials has to confirm this. 2. EXPERIMENTAL Fermentation Microorganism The strain of H. polymorpha transformed with the plasmid containing the lipolytic from F. heterosporum CBS 782.83 as described in EXAMPLE 2 was used in this study. The promoter used in the construct was the formate dehydrogenase promoter 20 from II. polymorpha.

Growth media and culture conditions YNB-glycerol medium The medium used for preparation of inoculum for the bioreactor fermentations and for 25 growth in shake flasks contained: 1.7 g/L Yeast Nitrogen Base (DIFCO. Detroit, USA, 0335-15-9), 5 g/L (NH^SCU, 10 g/L glycerol, and 0.1 M 2-[N-Morpholino]ethanesulfonic acid (MES) as a buffer. The pH was adjusted to 6.1 (the pKa of MES) with 4 M NaOH (before autoclaving). Yeast Nitrogen Base and (NH4)2S04 were filter-sterilized to the medium after autoclaving. This medium was 30 used for growth in shake flasks (250 mL medium in a shake flask with a total volume of 500 mL). 548497 89 YNB agar The defined medium used for plating of stock cultures (kept at -80°C in 25% (w/v) glycerol) contained: 1.7 g/L Yeast Nitrogen Base (DIFCO, Detroit, USA, 0335-15-9), 5 5 g/L (NH4)2S04, 10 g/L glycerol, and 20 g/L agar (DIFCO, Detroit, USA, 0140-01). Yeast Nitrogen Base and (NH4)2S04 were filter-sterilized to the medium after autoclaving.

YPD medium The rich medium was used for contamination check in the fermentors. The medium contained: 10 g/L yeast extract, 10 g/L peptone and 20 g/L glycerol.

Fermentations Three fermentations were carried out in this study: HET0401, HET0402 and 15 HET0410, all with the strain described above. The variations between the three fermentations are in the composition of the batch medium and the feed medium. All other parameters were identical for the three fermentations.

The batch medium (3L) used for the fermentation in 6 L fermentor contained: 13.3 g/L NH4H2PO4, 3.0 g/L MgS04H20, 3.3 g/L KC1, 0.3 g/L NaCl, 15 g/L glycerol, and 3 20 mL/L ADD APT® Foamstop Sin 260 (ADD APT Chemicals AG, Helmond, The Netherlands), 1.0 g/L CaCl22H20, 67 mg/L (NH4)2Fe(S04)2 6H20, 5 mg/L CuS04 5H20, 20 mg/L ZnS047H20, 21 mg/L MnS04H20, and 67 mg/L EDTA), 0.65 mg/L NiS04'6H20, 0.65 mg/L CoCl2, 0.65 mg/L H3BO4, 0.65 mg/L KI, 0.65 mg/L Na2Mo04'2H20), 2 mg/L D-biotin and 0.67 g/L thiaminchloride-hydrochloride. 25 In addition to the batch medium described above, fermentation HET0402 contained 10 g/L peptone in the batch medium.

In addition to the batch medium described above, fermentation HET0410 contained 10 g/L Bacto tryptone in the batch medium.

Feed medium HET0401 and HET0402: The feed medium contained 635 g/kg glycerol and 130 g/kg formic acid.

Feed medium HET0410: 548497 90 The feed medium contained 570 g/kg glycerol, 120 g/kg formic acid and 95 g/kg Bacto tryptone.

The pH was controlled by adding 25% (w/v) NHa-water.

The fermentation was carried out in the fed-batch mode in an in house build 6 L fermentor. The following fermentation conditions were used: pH 5, aeration 1 wm, temperature 26°C, and stirring from 400 to 700 rpm.

The fermentor was inoculated with 2*250 mL YNB-glycerol culture grown at 25°C and 180 rpm, and with an OD-6oo of approximately 10.

The feed flow in the fermentation was controlled by tire accumulated CO2 evolution, and based on the following equations: Feed ~ flow\g / /z] = 0, AcC02 < 0.45 Feed - flow\g / /z]~1.33 ■ V • AccC02,0.45 < AccC02 < 3.25 Feed - flow[g/ ft]-4.33 • V,3.25 < AccC02 V: The fermentation broth volume [l] AccC02 : The accumulated CO 2 evolution [moles] Harvest The fermentations were harvested by centrifugation for 10 minutes at 16000 x g followed by sterile filtration of the supernatant through 0.2 ^m filters (VacuCap 90 Filter Unit w 0.8/0.2 um Supor Membrane) from Gelman Laboratory. The product was kept at 4°C until use in baking trials.

Analytical procedures Determination of lipase activity A fermentation sample (10 mL) was centrifuged 9000 x g for 10 minutes, and the supernatant was used for the analysis of phospholipase activity according to the "PLU 25 assay" taught previously herein. 548497 91 Biomass growth The biomass concentration in a culture fluid was determined by centrifugation of 10 mL of culture fluid at 9000 x g for 10 minutes in a pre weighed container. After centrifugation, the supernatant was removed and the biomass was dried for 24 hours at 5 100°C and then weighed. The biomass concentration was calculated as g dry weight of cells per L culture fluid.

Enzyme characterisation and mini bakins Enzymes and flour Sample 205: Sample 7 (161 hours fermentation) from HET0401 Phospholipase Lipopan F, #2938 Flour: Reform 2003055 Minibaking The following ingredients were added to a 50 g Brabrender mixing bowl and kneaded for 5 minutes at 30°C: flour 50 g, dry yeast 10 g, sugar 0.8 g, salt 0.8 g, 70 ppm ascorbic acid and water (to a dough consistency of 400 Brabender units). Resting time was 10 min. at 34°C. The dough was scaled 15 g per dough. Then molded on a special device where the dough was rolled between a wooden plate and a Plexiglas frame. The 20 doughs were proofed in tins for 45 min. at 34°C, and baked in a Voss household oven for 8 min. 225°C.

After baking the breads were cooled to ambient temperature and after 20 min. The breads were scaled and the volume was determined by rape-seed displacement method. The breads were also cut and crumb and crust evaluated Lipid extraction g of fully proofed dough was immediately frozen and freeze dried. The freeze-dried dough was milled in a coffee mill and passed through a 800 micron screen. 1.5 g freeze-dried dough was scaled in a 15 mL centrifuge tube with screw lit. 7.5 ml water 30 saturated butanol (WSB) was added. The centrifuge tube was placed in a boiling water bath for 10 min. The tubes were placed in a Rotamix and turned at 45 rpm for 20 min. at ambient temperature. Then place in boiling water bath again for 10 min, and turn on 548497 92 the Rotamix for 30 min. at ambient temperature. The tubes were centrifiiged at 3500 g for 5 min. 5 ml supernatant was transferred into a vial. WSB was evaporated to dryness under a steam of nitrogen.

Gas chromatography Gas chromatography was performed as described under analytical procedures in example 1 above.

HPTLC Applicator: LINOMAT 5, CAMAG applicator.

HPTLC plate: 10 x 10 cm, Merck no. 1.05633 The plate is dried before use in an oven at 180°C for 20-30 minutes.

Application: l.OjxL of a 1% solution in CHC13:MeOH85:15 is applied to the HPTLC 15 plate using LINOMAT 5 applicator.

Running-buffer: No. IV: Chloroform : Methanol: H20 ( 65:25:4 ) No. I: P-ether : methyl-tert-butylether (MTBE) : Acetic acid (60:40:1) Application/Elution time: 11 minutes for running buffer I and 18 minutes for running buffer IV.

The plate is dried in an oven at 180°C for 10 minutes, cooled and developed in 6% cupri acetate in 16% H3PO4. Dried additional 10 minutes at 180°C and evaluated directly.

Baking trials Products tested: #3016 - Lipopan F containing 8700 LIPU/g ID Strain/host Fermentation 548497 93 Sample 206 containing 390 LIPU/g F. heterosporum/H. polymorpha HET0401+HET0402 Sample 209 containing 950 LIPU/g F. heterosporum/H. polymorpha HET0410 Recipe: Hard crusty rolls performed with Reform flour: 2003159 Bakers % Amount, g Flour- reform 2003159 100 2000 Water 58.5 1170 Compressed yeast 6 120 Salt 1.6 32 Sugar 1.6 32 Ascorbic acid lOppm 0.02 15 Standard alpha-amylase GRINDAMYL™ A 1000 90 ppm 0.180 Baking Procedure: Diosna mixer system • Dry mix for 1 min slow • Mix 2 min slow + 4 min fast • Dough temperature: 26°C 25 • Scaling: 1350 g • Resting: 10 min. at 30°C in heating cabinet • Moulding: Fortuna 3/17/7 • Proofing: 45 min. at 34°C, 85% RH.

• Baking: Bago oven: 13 min. at 220°C, 13sec. steam + 5 min damper open 30 • MIWE stone deck: prog, nr 1 548497 94 • After baking the rolls are cooled for 25 min before weighing and measuring of volume RESULTS AND DISCUSSION 5 Fermentation physiology and phospholipase production The addition of tryptone to the batch and feed medium of HET0410 resulted in a faster production of biomass and a higher final level of biomass compared to HET0401-. 0402.

HET0401 and HET0402 are almost identical with respect to the phospholipase activity development, whereas the phospholipase productivity is significantly higher in HET0410.

Harvest The fermentations were harvested after 168 hours (HET0401-0402) and 161 hours (HET0410) of fermentation. The product was kept at 4°C until use in baking trials. Some of the product of HET0401 was named sample 205, and contained approximately 700 PLU-7/mL. Some of the product from HET0401 and HET0402 was pooled and named sample 206. This product contained approximately 390 PLU-7/mL. 20 The lower enzyme activity of sample 206 compared to the end product of HET0401 and HET0402 may be caused by storage and sterile filtration. The product of HET0410 was named sample 209 and contained approximately 950 PLU-7/mL.

Enzyme characterization and mini baking Lipolytic enzyme sample 205 from fermentation HET0401 was tested in a minibaking experiment.

In different dosage and compared with a control and Lipopan F™. The specific bread volume of bread from this baking test is shown in Table 11. Picture of the bread are shown in Figure 11. 548497 95 Table 11 Lipolytic enzyme from Fusarium heterosporum (sample 205) in minibaldng experiments. Effect on bread volume.

Dosage Bread volume Sample PLU-7/kg flour mL/g 205 0 3.56 205 200 U/kg 3.98 205 500 U/kg 4.87 205 1000 U/kg .05 205 1500 U/kg .13 205 2000 U/kg 4.82 205 5000 U/kg .05 205 10000 U/kg 4.51 Lipopan F 40 ppm 4.57 The baking results confirmed a very strong effect of sample 205 on improvement of 5 bread volume, and the volume effect was better than Lipopan F™ in a standard dosage of 40 ppm.

From Figure 11 it is also seen that sample 205 contributes to a strong improvement in crumb structure and color.

Fully proofed dough from this baking experiment was freeze-dried and extracted with water saturated butanol, and the isolated lipids analyzed by GLC and HPTLC.

The GLC analysis of the dough lipids (Table 12) confirms the hydrolytic effect of 15 lipolytic enzyme sample 205 on digalactosyldiglyceride (DGDG) concomitant with an accumulation of digalactosylmonoglyceride (DGMG). The activity of the enzyme on DGMG is quite low because the total molar amount of DGDG (mmol% = mmol/100 g freeze-dried dough) and DGMG (mmol%) remains constant at increased enzyme dosage (Figure 12). The GLC results also indicate a very low activity of sample 205 on 20 triglyceride. 548497 96 Table 12 GLC analysis. of dough lipids. FFA= free fatty acid.

MGMG=monogalactosylmonoglyceride. DGMG digalactosylmonoglyceride. MGDG= monogalactosyldiglyceride. 5 DGDG=digalactosyldiglyceride. TRI— triglyceride Sample (S-) % % % % % % mmol% mmol% mmol% FFA MGMG DGMG MGDG DGDG TRI DGMG DGDG DGMG+ DGDG 0 U S-205 0.232 0.002 0.023 0.013 0.214 0.641 0.034 0.228 0.262 200 U S-205 0.321 0.007 0.050 0.038 0.193 0.660 0.074 0.205 0.279 500 U S-205 0.384 0.012 0.069 0.021 0.132 0.610 0.101 0.140 0.241 1000 U S-205 0.418 0.014 0.117 0.008 0.087 0.614 0.173 0.093 0.265 1500 U S-205 0.444 0.016 0.140 0.011 0.057 0.600 0.206 0.060 0.267 2000 U S-205 0.438 0.026 0.148 0.011 0.039 0.594 0.218 0.041 0.259 5000 U S-205 0.456 0.022 0.171 0.011 0.012 0.533 0.252 0.013 0.264 10000 U S-205 0.453 0.017 0.163 0.013 0.009 0.547 0.241 0.010 0.251 40 ppm Lipopan F 0.372 0.017 0.077 0.027 0.134 0.577 0.114 0.142 0.256 mmol% = mmol/100 g freeze-dried dough Comparing the baking results and the lipid analysis it is interesting to observe that the best baking effect is not obtained by a complete hydrolysis of DGDG to DGMG, but 10 the results indicate that a partly hydrolysis of DGDG to DGMG may give the best baking performance.

The high enzyme dosage produces more DGMG but also more free fatty acid is produced which is expected to give a negative baking effect, which might be another 15 explanation why only a partly hydrolysis of DGDG is preferable. Table 13 shows the ratio of DGDG and triglycerides hydrolysis, calculated from Table 12. The results illustrates that the best baking performance is obtained when at a dosage where the ratio of DGDG to triglycerides activity is greatest. 548497 97 Table 13. Ratio of DGDG and triglyceride hydrolysis from GLC analysis of dough lipids.

Sample (S) dTRI dDGDG dDGDG/dTRI Bread volume mL/g 0 U S-205 3.56 200 U. S-205 0 0.023 3.98 500 U S-205 0.031 0.088 2.84 4.87 1000 U S-205 0.027 0.135 0.030 .05 1500 U S-205 0.041 0.168 4.1 .13 2000 U S-205 0.047 0.187 3.98 4.82 5000 U S-205 0.108 0.215 1.99 .05 10000 U S-205 0.094 0.218 2.3 4.51 40 ppm Lipopan F 0.064 0.086 1.34 4.57 Some of the lipid samples were also analyzed by HPTLC as shown in Figure 13. Sample 4, 5 and 6 are dough lipids from the baking experiment. The HPTLC analysis confirms the hydrolysis of DGDG and formation of DGMG by lipolytic enzyme sample 205.

The relative polar lipid:triglyceride activity ratio of Lipopan F and Sample 209 using the assays taught hereinabove are: Phospholipid/triglyceride (PLU/LIPU) Lipopan F = 3 15 Sample 209 = 9 Galactolipid/triglyceride (GLU/LIPU) Lipopan F = 1 Sample 209 - 4 548497 98 Fusarium heterosporum CBS 782.83 lipolytic enzyme gave very strong effects in miniscale baking experiments with strong increase in bread volume and improvement of crumb structure. Lipid analysis confirms strong hydrolytic activity on DGDG in dough concomitant with the accumulation of DGMG. Fusarium heterosporum CBS 5 782.83 lipolytic enzyme showed low activity on triglycerides in a dough.

Example 4. Characterization of activity on lipid substrates and position specificity of a Fusarium heterosporum CBS 782.83 lipolytic enzyme expressed in Hansenula polymorpha.

A lipolytic enzyme according to the present invention from Fusarium heterosporum was expressed in Hansenula polymorpha as described in Example 3.

Analytical procedures Phospholipase activity was determined using the PLU assay described previously herein.

Galactolipase activity was determined using the galactolipase assay described previously herein.

Activity on triglyceride (tributyrin) was determined using the LIPU assay described previously herein.

Activity on sunflower oil (LUSol. pH-stat pH 6): Reagents: 8,4 g gum arabic is dissolved in 100 ml deionized water and 100 ml 30 mM CaCl2 is added. 36 g sunflower oil is slowly added during mixing with a Turrax mixer (20000 rpm) Assay: ml sunflower oil emulsion in a beaker is equilibrated at 30°C for 5 min. pH is adjusted to 6,3-6,5 using a pH stat. 2 ml enzyme solution is added, and 0.05 N NaOH 548497 99 is continuously added keeping the pH at 6.5 for 10 minutes. The slope of the curve for the addition of 0.05 NaOH as a function of time is calculated. 1 LUSol is defined as the quantity of enzyme, which can liberate 1 pmol fatty acid per min. under assay conditions The lipolytic enzyme was analysed for activity on different substrates according to procedures mentioned above. The results are shown in Table 14.

Table 14, Activity of a lipolytic enzyme Fusarium heterosporum according to the 10 present invention on different lipid substrates.

Activity Substrate pH Temperature UNIT/ml LIPU Tributyrin .5 754 LUSol Sunflower oil 6.5 48 PLU-7 Phosphatidylcholine 7 37 4650 GLU Digalactosyldiglyceride 7 37 1600 The lipolytic enzyme from Fusarium heterosporum expressed in Hansenula polymorha hydrolysis primarily fatty acids in the sn-1 position of galactolipid and phospholipids in dough. The specificity of the enzyme was investigated by adding different concentrations of the enzyme to a bread dough. The fully proofed dough was frozen and freeze dried, and the dough lipids were extracted with water saturated butanol.

The dough lipids were analysed by GLC and HPLC analysis.

By GLC analysis it was possible to analyse digalactosyl diglyceride(DGDG) and digalactosylmonoglyceride(DGMG). Further it was possible to analyse the position isomers of digalactosyl monoglyceride (lrdigalactosyl 1-monoglyceride and 2: digalactosyl 2-monoglyceride, see structure below). These components were separated and quantified by GLC. 548497 WO 2005/087918 PCT/IB2005/000875 100 1: R1 == H and R2= Fatty acyl ch2oh ch 20c0r r £ oc 0 ch I ch 20 0—1 oh ch2° j 0 1 oh 0h \y oh 2: R1 - Fatty acyl and R2=H ch 2 oh In a baking test for production of hard crust rolls different dosages of the lipolytic enzyme were added and galactolipids in the fully proofed dough were analysed. The amount of the isomer digalactosylmonoglycerides are shown in Table 15 and illustrated graphically in Figure 14. 548497 101 Table 15. Amount of isomer digalactosylmonoglycerides in a baking test using lipolytic enzyme from Fusarium heterosporum Enzyme dosage Digalactosyl 2-monoglyceride Digalactosyl 1-monoglyceride TP U/kg flour %, based on dough dry weight %, based on dough dry weight 0 200 400 400 800 1000 1200 1500 2000 0,0102 0,0092 0,0071 0,0067 0,0103 0,0071 0,0081 0,0064 0,0084 0,0399 0,0167 0,0100 0,0057 0,0063 0,0060 0,0053 0,0057 0,0047 Conclusion From the results in Table 15 and Figure 14 it is concluded that digalactosyl diglyceride is primarily hydrolysed in 1-position during production of digalactosyl 2-monoglyceride. A smaller increase in the amount of digalactosyl 1-monoglyceride is also observed. It is well known that acyl migration from 2 to 1 position of acyl fatty 10 acid in lipids will occur. This acyl migration depends on temperature and as a function of time an equilibrium between digalactosyl-2-monoglyceride and digalactosyl 1-monoglyceride will occur. This phenomena explains the fact that a small increase in digalactosyl 1-monoglyceride also is observed.

Example 5. Determination of temperature optimum and stability of lipolytic enzyme derived from Fusarium heterosporum.

The enzyme activity of spray dried lipolytic enzyme derived from F. Heterosporum and expressed in Hansenula Polymorpha was determined at various temperatures according to 20 PLU-7 with modifications as described below. The substrate was an emulsion of 0.6% phosphatidylcholin, 0.4% Triton X-100, 6 mM CaCk, and 50 mM HEPES, pH 7.0. The 548497 102 spray dried lipolytic enzyme ferment was diluted with demineralised water to 3 TIPU/ml. 400 j-il of substrate was thermostatted for 5 minutes at 10, 20, 30, 40, 50, 45, 50 and 60°C and 50 |il sample was added. After exactly 10 minutes, the enzymation was stopped by incubation at 99°C for another 10 minutes. Finally, the amount of free fatty acids was 5 determined by NEFA C method (Wako Chemicals GMbH, Neuss, Germany). Colour reagent A and B was made according to manufacturers protocol. 10 fil redispersed extracted lipid and 100 pi reagent A were pipetted to a microtiter plate and incubated at 37°C for 10 minutes. 200 pi reagent B was added to the microtiter plate and incubated at 37°C for 10 minutes. The optical density at 540 run was measured. The amount of free 10 fatty acid was determined, using the read absorbance and a standard curve based on oleic acid. Results are shown in Figure 15.

Enzyme stability of spray dried lipolytic enzyme ferment was determined at various temperatures. Spray dried lipolytic enzyme ferment was diluted with 50 mM phosphate 15 buffer, pH 7.0 to 3 TIPU/ml. After 30 minutes of incubation at 20, 30, 37, 40 and 45°C the sample was stored on ice. Subsequently, phospholipase activity was determined according to PLU-7 with modifications as described below. The substrate was an emulsion of 0.6% phosphatidylcholin. 0.4% Triton X-100, and 50 mM phosphate buffer.. CaCl2 was left out to prevent precipitation of calcium phosphate and does not affect the enzyme activity. 400 20 pi of substrate was thermostatted for 5 minutes at 37°C and 50 pi sample was added. After exactly 10 minutes, the enzymation was stopped by incubation at 99°C for another 10 minutes. Finally, the amount of free fatty acids was determined by the NEFA C method (Wako Chemicals GmbH, Neuss, Germany). Colour reagent A and B was made according to manufacturer's protocol. 10 pi redispersed extracted lipid and 100 pi reagent A were 25 pipetted to a microtiter plate and incubated at 37°C for 10 minutes. 200pl reagent B was added to the microtiter plate and incubated at 37°C for 10 minutes. The optical density at 540 nm was measured. The amount of free fatty acid was determined using the red absorbance and a standard curve based on oleic acid. Results are shown in Figure 16. 548497 103 Example 6. Determination of pH optimum and stability of a lipolytic enzyme derived from Fusarium heterosporum.

The enzyme activity of spray dried lipolytic enzyme derived from F. heterosporum and 5 expressed in Hansenula Polymorpha was determined at various pH. The substrate was an emulsion of 0.6% phosphatidylcholin, 0.4% Triton X-100, and 50 mM phosphate buffer pH 4.0, 5.0, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, 9.0 and 10.0. CaCk was left out to prevent precipitation of calcium phosphate and does not affect the enzyme activity. The spray dried lipolytic enzyme ferment was diluted with demineralised water to 3 TIPU/ml. 400 p.1 10 of substrate was thermostatted for 5 minutes at 37°C and 50 ul sample was added. After exactly 10 minutes, the enzymation was stopped by incubation at 99°C for another 10 minutes. Finally, the amount of free fatty acids was determined by NEFA C method (Wako Chemicals GMbll, Neuss, Germany). Colour reagent A and B was made according to manufacturers protocol. 10 jj.1 redispersed extracted lipid and 100 |_il reagent A were 15 pipetted to a microtiter plate and incubated at 37°C for 10 minutes. 200 ul reagent B was added to the microtiter plate and incubated at 37°C for 10 minutes. The optical density at 540 nm was measured. The amount of free fatty acid was determined, using the read absorbance and a standard curve based on oleic acid. Results axe shown in Figure [17].

The enzyme stability of spray dried lipolytic enzyme ferment was determined at various pH. Spray dried lipotytic enzyme ferment was diluted with 50 mM phosphate buffer at pH 4.0, 5.0, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5, 9.0 and 10.0 to 3 TIPU/ml. After 30 minutes of incubation at 37°C the sample was stored on ice. Subsequently, the phospholipase activity was determined according to PLU-7 with modifications as described below. The substrate 25 was an emulsion of 0.6% phosphatidylcholin, 0.4% Triton X-100, and 50 mM phosphate buffer, pH7. CaCl2 was left out to prevent precipitation of calcium phosphate and does not affect the enzyme activity. 400 jj.1 of substrate was thermostatted for 5 minutes at 37°C and 50 i_l1 sample was added. After exactly 10 minutes, the enzymation was stopped by incubation at 99°C for another 10 minutes. Finally, the amount of free fatty acids was 30 determined by the NEFA C method (Wako Chemicals GmbH, Neuss, Germany). Colour reagent A and B was made according to manufacturers protocol. 10 p.1 redispersed 548497 104 extracted lipid and 100 jxl reagent A were pipetted to a microtiter plate and incubated at 37°C for 10 minutes. 200jal reagent B was added to the microtiter plate and incubated at 37°C for 10 minutes. The optical density at 540 nm was measured. The amount of free fatty acid was determined using the read absorbance and a standard curve based on oleic 5 acid. Results are shown in Figure 18.

Example 7. Determination of molecular weight of purified lipolytic enzyme derived from Fusarium heterosporum Purified lipolytic enzyme according to the present invention derived from Heterosporum Fusarium was run on an SDS-PAGE gel, Figures 19a and 19b. Based on a Novex standard marker, the molecular weight was calculated as shown in Table 15 Table 15: Determination of the molecular weight of the lipolytic enzyme according to the present invention Sample Rf ^ Calculations L (kDa) Mw n Afi Log Mw (kDa) - -5,30-Rf3 + 7,50-Rf2 - 5,00-Rf + 2,7986 0.78 r2 = 0,9989 1.15 1.23 1.45 1.58 1.69 1.79 1.99 2.27 Lipolytic enzyme according to the 0.52 present invention Novex standard 0.91 3.0 0.82 6.0 0.71 14 0.66 17 0.55 28 0.47 38 0.38 49 0.31 62 0.23 98 0.13 188 log Mw - -5.30-0.523 + 7.50-0.522 - 5.00-0.52 + 2.80- => Mw = 29.9 kDa The weight of the lipolytic enzyme was calculated to 29.9 kDa. 548497 105 Example 8. Determination of the isoelectrical point (pi) of lipolytic enzyme derived from Fusarium heterosporum.

The isoelectrical point (pi) of a lipolytic enzyme derived from F. heterosporum was 5 determined theoretically based on the amino acid sequence SEQ ID NO. 6.

The calculation was made using the software Vector NTI Suite 9 from Informax (Invitrogen, CA, USA) and resulted in a pi of 6.40.

EXAMPLE 9. Characterization of enzymatic conversion of lecithin to lysolecithin in egg yolk at different temperatures by a Fusarium heterosporum CBS 782.83 lipolytic enzyme.

Lipolytic enzymes can convert lecithin (phosphatidylcholine) to lyso-lecithin (lyso-15 phosphatidylcholine) with release of a free fatty acid. Enzymatic conversion of lecithin to lyso-lecithin in egg yolk creates better emulsifying properties because lysolecithin is a better emulsifier than lecithin. Good emulsifying properties of egg yolks are of importance when making heat stable mayonnaise and other foods and food applications, such as, but not limited to, cakes and maturation of cheese.

Enzyme preparation: A lipolytic enzyme from Fusarium heterosporum, CBS 782.83, expressed in Hansenula polymorpha from fermentation HET0420 was spray dried on wheat starch . The resulting enzyme preparation had a phospholipase activity of 1265 U/g, 25 determined by TIPU assay previously described herein.. A 10% (w/v) or 20% (w/v) enzyme stock solution was prepared by dissolving the spray dried enzyme powder in demineralised water. After 15 minutes of stirring, the solution was centrifuged for five minutes at 1370 x g. The supernatant was used as the enzyme stock solution.

Enzymation: Two different experiments were set up to determine the optimal combination of enzyme dosage, reaction temperature and time for the enzymatic conversion of lecithin 548497 106 to lyso-lecithin in egg yolk. In the first, enzymation was carried out with a lipolytic enzyme according to the present invention at the three following temperatures: 30°C, 40°C and 50°C, each with the four following dosages: 5 U/g egg yolk, 10 U/g egg yolk, 20 U/g egg yolk and 30 U/g egg yolk.

In the second experiment, enzymation was carried out for a lipolytic enzyme according to the present invention and with Lecitase® Ultra from Novozymes A/S (Denmark), respectively, at the following five temperatures: 5°C, 10°C, 15°C, 20°C, and 53°C with an enzyme dosage of 30 U/g egg yolk. At 53°C the enzyme dosage of 60 U/g egg yolk was also tested.

In both experiments, 10.0 g pasteurised egg yolk from Dan/£g (Christiansfeld, Denmark) was transferred to a Wheaton tube and placed in a heating block thermostatted to the appropriate temperature. The samples were continuously mixed on a magnetic stirrer. At time t=0 enzyme stock solution was added to the egg yolk according to Table 16. Each experiment was made in duplicate. 1.0 g samples were taken from the egg yolk/enzyme solutions according to Table 17. After incubation times according to Table 17, the enzymatic reaction in the samples was stopped by adding 7.5 ml organic solvent (CHCl3:MeOH, 2:1).

Table [16]: Enzyme stock solution was added to egg yolk to obtain different enzyme dosages, including a control. Demineralised water was added to a total of 2.35 ml to disregard any difference in volume upon addition of different volumes of enzyme stock solution.

Sample Amount egg yolk Enzyme activity Enzyme activity of stock solution Volume enzyme stock solution added Volume dem. H2O added Control .0 g 0 U - 0 ml 2.35 ml .0 g SOU 127 U/ml 0.40 ml 1.95 ml Lipolytic .0 g 100 U 127 U/ml 0.80 ml 1.55 ml enzyme .0 g 200 U 127 U/ml 1.60 ml 0.75 ml .0 g 300 U 127 U/ml 2.35 ml 0 ml 548497 107 .0 g 600 U 253 U/ml 2.35 ml 0 ml Lecitase® 10.0 g 300 U 3620 U/ml 83 jil 2,25 ml Ultra 10.0 g 300 U 3620 U/ml 165 ^1 2,20 ml Table [17]: Reaction times at sample extraction in the different experiments.

Reaction temperature Enzyme dosage Reaction time (min) °C, 10°C, 15°C, 20°C U/g 5,10,20 and 30 60 120 240 360 480 1440 - °C 40°C U/g ,10,20 and 30 U/g , 10,20 and 30 U/g 30 U/g 30 60 60 120 120 240 240 360 360 - 50°C 53°C 15 60 120 60 240 90 360 -120 240 53°C 60 U/g 60 90 120 240 330 Lipid extraction: Addition of 7.5 ml organic solvent (CHCl3:MeOH, 2:1) to the sample not only stopped the enzyme reaction but also extracted the lipids. Furthermore, 0.2 ml demineralised H2O was added to the sample before it was dispersed, using a Whirley mixer for 1 minute. The sample was then centrifuged for ten minutes at 110 x g. Approximately 3 10 ml of the organic phase was transferred to another tube and this extracted lipid was used for various analyses. The samples were stored at -18°C.

Determination of free fatty acids: 100 pi of the extracted lipid solution was evaporated under nitrogen at 50°C. 1.0 ml 15 demineralised H2O was added and the lipid was dispersed using a Whirley mixer. The amount of free fatty acid was determined using the NEFA C kit from WAKO Chemicals GmbH (Neuss, Germany). Colour reagent A and B were made according to 548497 108 manufacturers protocol. 10 pi redispersed extracted lipid and 100 pi solution A were pippetted to a microtiter plate. The plate was incubated at 37°C for 15 minutes. 200 pi solution B was added to the microtiter plate, and the plate was incubated at 37°C for 10 minutes. The optical density at 540 nm was measured. The amount of free fatty acid 5 was determined, using the read absorbance and a standard curve based on oleic acid.

Determination of lecithin and lyso-lecithin by LC/MS-MS: Materials Acetone, methanol, chloroform were all from Lab Scan, Dublin, Ireland, ethanol 96% 10 was from De Danske Spritfabrikker, and formic acid was from AppliChem, Darmstadt, Germany.

Instrumentals The HPLC system consisted of a quarternary pump (G1311A), a capillary pump 15 (G1376A), an autosampler (G1377A), and a column compartment (G1316A) all from Agilent Technologies (Waldbronn, Germany). An Acurate™ flowsplitter (ACM-CU-CR) from LC Packings (Amsterdam, Netherlands) was used to split the column effluent to the mass spectrometer and to introduce polar make-up solvent. The mass spectrometer was an LCQ Deca Ion Trap from Thermo Finnigan (San Jose, CA, USA).

The column was a Hypersil SI, 100 x 4.6 mm id, 5pm from Thermo Hypersil-Keystone.

Chromatogi'aphic and MS conditions Mobile phases A: — not used 25 B: Chloroform C: Methanol / Formic Acid (1000/0,190) D: Chloroform/MethanolAVater/Formic Acid (300/550/150/0,190) Make-up: Ethanol 96% ~ , 548497 „ , WO 2005/087918 PCT/IB2005/000875 109 Flow Time B C D [ml/min] [min] [%] [%] [%] 0.6 0 40 60 0 0.6 2 0 0 100 0.6 8 0 0 100 0.6 9 40 60 0 0.6 16 40 60 0 Tlie injection volume was 5|il and the column temperature was 45°C.

Flow splitter LC-flow MakeuD-flow ~ LC-flow: Make-up flow: ELSD/FC tubing: MS tubing: -► ELSD/FC -► MS 0.60 ml/min 100 pl/min 100 cm x 0.100 mm id (SS) 100 cmx 150 [im (FS-150-MS) Approximate split is 20:1 MS conditions MS parameter settings: Parameter Value Capillary temp [°C] 325 Sheath gas flow 70 Auxiliary gas flow 4 Source ESI Polarity Positive Source voltage [kV] 6.0 SIM micro Scans 5 SIM Max Ion Time [ms] 200 548497 110 MS detector setting: Parameter Value Duration [min] Tune method LPC_544_SIM_00.LCQTun e Scan Event 1 - SIM Ranges Mass Interval LPC(16:0) -If 494.0-498.0 LPC (18:2) -H1" 517.0-527.0; 541.0-549.0 PC (34:2) -H+ 778.0 - 786.0 PC (36:4) - H+ 801.0-813.0 Standard and sample preparation Lyso-phosphatidylcholine (LPC) (Egg, chicken) (89865) and phosphatidylcholin (PC) 5 (plant) (441601) were from Avanti Polar Lipids, Inc, Alabaster, AL, USA. A stock solution of PC and LPC (10 mg/20 ml CHCk/MeOH) was prepared. Dilutions hereof were prepared to cover the concentrations from 50 ng/ml to 2.5 pg/ml. 7.5 pi lipid extract from 1 g of egg yolk was reconstituted in 1.5 ml CHC^MeOH (1:1).

TLC analysis: The TLC analysis was carried out as described in Example 1.

For visualisation of the different glycerides, 2 pi lipid extract was applied in 3 mm bands to a HPTLC silica 60 plate (Merck) by an automatic TLC sampler 4 (CAMAG). The silica plate was placed in a horizontal developing chamber (CAMAG) with 15 running buffer I (P-ether: methyl tertiary butyl ether:acetic acid (50:50:1)). 20 ml running buffer was used for the gas phase and 5 ml for the through and the plate was eluted until approx. 5 cm from the application position. The plate was dried in a heating cupboard (160°C) for 5 minutes. Finally, the TLC plate was immersed in the developing reagent (6% Cu(CH3COO)2 in 16% aqueous H3PO4) and carbonised in a 20 heating cupboard (160°C) for 10 minutes. 548497 111 RESULTS To determine the optimal combination of enzyme dosage, reaction temperature and time for the enzymatic conversion of lecithin to lyso-lecithin in egg yolk four different enzyme dosages were tested at three different temperatures and five different reaction 5 times.

The four enzyme dosages used, 5 U/g, 10 U/g, 20 U/g, and 30 U/g, as well as tlie reaction times used, 30 minutes, 60 minutes, 120 minutes, 240 minutes, and 360 minutes, were based on initial trials not covered herein. The three temperatures, 30°C, 10 40°C, and 50°C, were chosen based on the temperature optimum curve for the lipolytic enzyme, see Figure 20.

The amount of lecithin and lyso-lecithin in enzyme modified egg yolk was analyzed by HPLC and depicted in Figure 21 and Figure 22 as a function of reaction time. In Figure 23, the amount of free fatty acid in enzyme modified egg yolk is depicted as a 15 function of reaction time.

The experiment shows that conversion of lecithin to lyso-lecithin by a lipolytic enzyme according to the present invention was optimal using 20 U/g egg yolk of the lipolytic enzyme at 30°C for 120 minutes. The dosage of 20 U/g egg yolk is chosen 20 due to an observed decrease in LPC levels at 30 U/g egg yolk from 120 minutes of reaction to 240 minutes of reaction.

Based on this result, it was examined whether the lipolytic enzyme according to the present invention and Lecitase® Ultra have an effect on egg yolk lipids at 25 temperatures lower than 30°C and to compare their activities at 53 °C, which is the temperature currently used industrially for Lecitase® Ultra.

The enzymatic conversion of lecithin to lyso-lecithin in egg yolk was tested at five different temperatures (5°C. 10°C, 15°C, 20°C, and 53°C) and six different reaction 30 times. An enzyme dosage of 30 U/g egg yolk was tested because this would be the highest dosage of commercial interest due to cost of the enzyme and because reaction 548497 112 rates were expected to be low at the temperatures tested. All enzyme units mentioned have been determined by TIPU. 30 U/g egg yolk is also the recommended dosage of Lecitase® Ultra. In addition, a dosage of 60 U/g egg yolk was tested at 53°C. The reaction times used were 60 minutes, 120 minutes, 240 minutes, and 360 minutes, 480 5 minutes and 1440 minutes. However, at 53°C the reaction times were 15 minutes, 30 minutes, 60 minutes, and 90 minutes, 120 minutes and 240 minutes. At 53°C using 60 U/g a sample was also taken at 330 minutes of reaction.

In Figures 24 and 25 the amount of lyso-lecithin, free fatty acid, and lecithin in 10 enzyme-modified egg yolk is depicted as a function of reaction time using the lipolytic enzyme according to the present invention and Lecitase® Ultra phospholipases, respectively. The lecithin and lyso-lecithin contents of the samples were determined by LC-MS and the free fatty acid content was determined by the NEFA C method. The amount of FFA in the control samples (results not shown) and the sum of lyso-lecithin 15 and lecithin remained constant during the experiments shown in Figures 24 and 25.

Figure 24 shows the results of enzymation of egg yolk with the lipolytic enzyme according to the present invention. At 53°C the activity of the lipolytic enzyme ceased after 30 minutes of reaction reaching a level of LPC of 1.7% (w/w) with 30 U/g egg 20 yolk (Figure 24b). The levels of FFA were 1.0% (w/w) and 1.3% (w/w) with 30 U/g egg yolk and 60 U/g egg yolk, respectively. Using Lecitase® Ultra, the amounts of LPC and FFA increased during the period 15-240 minutes (figure 19), yielding 2.7% LPC (w/w) after 240 minutes of reaction with 30 U/g egg yolk. The levels of FFA were 1.4% (w/w) and 2.1% (w/w) after 240 minutes of reaction using 30 and 60 U/g 25 egg yolk, respectively. The activity of Lecitase® Ultra ceased after 330 minutes of reaction using 60 U/g egg yolk. The lipolytic enzyme of the present invention had a higher initial reaction rate than Lecitase® Ultra.

At 20°C and 53°C the initial reaction rates were similar with the lipolytic enzyme of 30 the present invention (figure 24). At temperatures 5-20°C the amount of LPC and FFA increased during the experiment. Although at temperatures below 20°C the initial velocity decreased markedly with decreasing temperatures. At 20°C a LPC level of 548497 113 3.3% (w/w) and a FFA level of 1.6% (w/w) was reached after 60 minutes of reaction with 30 U/g egg yolk. This level was similar to 240 minutes of reaction at 53 °C with Lecitase® Ultra. It was not possible to resuspend the solvent-free lipid extract for FFA analysis after 1440 of reaction at 20°C. After 1440 minutes at 5°C and 10°C the 5 samples with the lipolytic enzyme had a high viscosity which made stirring impossible. This was most likely due to crystallisation of FFA. The decrease in LPC levels which was seen in TN 6642 at 30 U/g egg yolk, 30°C from 120 to 240 minutes of reaction was not observed in any of these experiments.

Enzymation of egg yolk with Lecitase® Ultra phospholipase gives significantly decreasing initial velocities at 20°C and temperatures below compared to the initial velocity of Lecitase® Ultra at 53°C (figure 25). At 20°C a LPC level of 3.0% (w/w) and a FFA level of 1.5% (w/w) was reached after 1440 minutes of reaction with 30 U/g egg yolk. This level was similar to 240 minutes of reaction at 53°C.

Figure 26 shows TLC analysis of extracted lipid from enzyme modified egg yolk. This analysis confirmed the results from LC-MS and showed that the lipolytic enzyme according to the present invention and Lecitase® Ultra phospholipase increased the amount of lyso-lecithin.

The enzymatic reaction, which is catalysed by lipolytic enzymes, produces equivalent amounts of lyso-lecithin and free fatty acids. A possible and unwanted side reaction is hydrolysis of triacylglycerides. The relation between change in amount of lyso-lecithin and free fatty acids during the enzymatic reaction is shown in Figure 27.

With Lecitase® Ultra there is a good correlation of equivalent formation of lysolecithin and free fatty acids (figure 27). However, in most samples treated with Lecitase® Ultra there was very little reaction. Enzymation of egg yolk with the lipolytic enzyme of the present invention results in production of more than one free fatty acid per lyso-lecithin formed at lyso-lecithin levels above 40 mM and free fatty acid levels above 60 mM. The maximal conversion with Lecitase® Ultra is 30 mM lyso-lecithin and 25 mM free fatty acid. Samples with a free fatty acid to lyso-lecithin 548497 114 ratio below 0.8 or above 1.2 (n/n) and LPC content above 1.0% (w/w) are shown in table 18.

Table 18: Samples with free fatty acid (FFA) to lyso-lecithin (LPC) ratios below 0.8 or 5 above 1.2 (n/n) and LPC content above 1% (w/w). The samples were treated with lipolytic enzyme or Lecitase® Ultra. FFA was determined by the NEFA C method. LPC and PC was determined by LC-MS.

Temp.

Reaction AFFA/ALPC %LPC %FFA %PC Enzyme (°C) time (min) (n/n) (w/w) (w/w) (w/w) Lipolytic enzyme 1440 1.99 3.0 2.9 2.0 Lipolytic enzyme 480 1.97 2.3 2.3 2.5 Lipolytic enzyme 480 1.48 4.1 3.5 0.6 Lipolytic enzyme 360 1.64 3.6 3.4 1.0 Lipolytic enzyme 1440 1.98 4.2 4.7 0.1 Lipolytic enzyme 60 0.67 3.3 1.6 2.0 Lipolytic enzyme 360 1.30 4.7 3.6 0.3 Lipolytic enzyme 480 1.43 .0 4.1 0.3 Lecitase® Ultra 1440 0.72 3.0 1.5 2.0 Lipolytic enzyme 53 0.69 1.5 0.9 3.7 Lipolytic enzyme 53 60 0.70 1.7 1.0 2.6 Lipolytic enzyme 53 90 0.71 1.8 1.0 2.7 Lipolytic enzyme 53 240 0.72 1.7 1.0 2.8 Lipolytic enzyme 53 0.72 1.8 1.0 3.0 Lecitase® Ultra 53 120 0.61 2.4 1.1 2.3 Lecitase® Ultra 53 60 0.62 1.6 0.9 2.9 548497 115 Samples with a free fatty acid to lyso-lecithin ratio above 1.2 (n/n) and LPC content above 1.0% (w/w) (figure 27) are generally seen at prolonged reaction times or in samples containing less than 1.0% PC (w/w). The lipolytic enzyme sample at 15°C has elevated free fatty acid to lyso-lecithin ratios in all samples. This indicates that the 5 enzymes change substrate specificity at prolonged reaction times or when the content of PC is low. This could be due to hydrolysis of phosphatidylethanolamine. digalactosyl diacylglyceride, or triacylglycerides that are found in egg yolk. Samples with a free fatty acid to lyso-lecithin ratio below 0.8 (n/n) and LPC content above 1.0% (w/w) are generally seen at a reaction temperature of 53°C (Table 18). This 10 could be explained by interesterifications.

Figure 28 shows that the lipolytic enzyme of the present invention does have hydrolytic activity on triacylglycerides and 1,3 diacylglycerides at prolonged reaction times or low concentrations of PC. The accumulation of 1,2 diacylglycerides shows 15 that the lipase activity is 1,3-specific. The formation of monoglycerides shows that Lecitase® Ultra had a hydrolytical effect on tri- or diacylglycerides at 20°C. It is not possible to determine whether the lipolytic enzyme of the present invention or Lecitase® Ultra phospholipase has the highest degree of hydrolysis of triacylglycerides because the levels of formation of LPC differ significantly. Lowering 20 the enzyme dosage and reaction time of lipolytic enzyme could reduce the hydrolysis.Table 18A shows the reaction time, temperature and dosage applied to the subjects of lanes 1-30 in Figure 28.

Table 18A Irane number I 2 4 6 B 9 11 12 13 14 16 17 18 19 21 22 23 24 26 27 28 29 | Eozjme* B K K L B K K L B K K K K K K L L L L B K K K U L L B K L 9 3 Q £ Reaction time (h) 8 24 24 8 24 24 8 24 g 24 4 6 24 1 2 4 1 2 4 4 4 ' Temperature (°C> 53 53 53 53 53 53 53 53 53 53 &OS02C fU/a) 3D 3D 3(1 69 60 60 *) B: Blank, K: Llnolvtie protein according to the crcssnt invention. L: Lecitase® Ultra phospho rase It will be apparent to tlie skilled person that, using routine experimentation, optimisation of enzyme dosage, reaction temperature and reaction time may be readily determined for any given food application. 548497 116 Conclusion Enzymation of egg yolk from DanJEg A/S of a lipolytic enzyme according to the present invention and Lecitase® Ultra phospholipases was carried out to determine the conversion of lecithin to lyso-lecithin. This was done using an enzyme dosage 30 U/g 5 egg yolk at five temperatures (5-20°C, and 53°C), and six different reaction times (60-1440 minutes, however at 53 °C, 15-240 min) was carried out to examine the enzyme activity. 53 °C is the temperature currently used in the industry for modifying egg yolk with Lecitase® Ultra.

The lipolytic enzyme according to the present invention had a higher initial reaction rate than Lecitase® Ultra at all temperatures tested. At 53°C reaction with lipolytic enzyme ceased after only 30 minutes of reaction. At a dosage of 30 U/g egg yolk at 53°C the LPC level was 1.7 and 2.7% (w/w) with lipolytic enzyme and Lecitase® Ultra, respectively. A level of 3.3% (w/w) LPC was reached after only 60 minutes of 15 reaction at 20°C with lipolytic enzyme.

At low temperatures (5-20°C) the conversion of lecithin to lyso-lecithin with lipolytic enzyme was significantly better than with Lecitase® Ultra. The reaction velocity of the lipolytic enzyme was markedly lower at 10°C and below compared to at 15°C and 20 above. The lipolytic enzyme was active at 5°C and formation of more than 2% (w/w) lyso-lecithin was detectable after 24 hours of reaction. Also, the samples with the lipolytic enzyme were more viscous at 10°C and below compared to higher temperatures.

The lipolytic enzyme was found to change substrate specificity and hydrolyse phosphatidyl-ethanolamine, digalactosyl diacylglyceride, or triacylglycerides in addition to phospholipids at prolonged reaction times or when the content of PC is low. This may be avoided by using a lower enzyme dosage and shorter reaction times and substantiates the need for thorough optimization of conditions of treatment for 30 each product in question. At 53°C interesterifications can explain that less than one equivalent free fatty acid per lyso-lecithin is produced with lipolytic enzyme and Lecitase® Ultra. 548497 117 In conclusion, the lipolytic enzyme according to the present invention is a potential candidate for enzymation of egg yolk at low temperatures. The observed activity at low temperatures is also of interest in other applications.

EXAMPLE 10. Production of mayonnaise by use of a Fusarium heterosporum CBS 782.83 lipolytic enzyme.

Production of mayonnaise: 6.25 g lipolytic enzyme prepared as described in Example 4 was dissolved in 50 mL demineralised H2O corresponding to a phospholipase activity of 150 U/mL. After 15 minutes of stirring, the solution was centrifuged for five minutes at 1370 x g. The supernatant was used for enzymation of 150 g egg yolk from Sanofa A/S according to Table 19. Another 150 g egg yolk from Sanofa A/S was treated with Lecitase© Ultra 15 (Novozymes A/S, Denmark) according to Table. The enzymations were carried out at 30°C for 180 minutes with slow agitation. Lipid extraction was carried out as described in Example 4.

Table 19: Enzymation of egg yolk from Sanofa A/S using lipolytic enzyme according 20 to the present invention and Lecitase® Ultra, respectively. The lipolytic enzyme solution used had an activity of 150 U/mL, and the Lecitase® Ultra had a phospholipase activity of 34500 U/mL.

Sample Amount egg yolk Lipolytic enzyme added Lecitase® Ultra added Dem H20 added U/g egg yolk Control 150 g .0 mL 0 Lipolytic enzyme 150 g .0 mL Lecitase® Ultra 150 g 0.13 mL 29.9 mL Mayonnaise with enzyme-modified egg yolk from Sanofa A/S was produced using a Korurna mixer (Disho V60/10). During processing the mayonnaise was heated to 95°C for five minutes. 548497 118 Table 20: Ingredients used to produce mayonnaise.

Ingredient Mayonnaise Control Mayonnaise Lipolytic enzyme Mayonnaise Lecitase® Ultra Water 34.5 % 34.5 % 34.5 % Oil 50.0 % 50.0 % 50.0 % Salt 1.0% 1.0 % 1.0% Sugar 3.0 % 3.0 % 3.0 % Potassium Sorbate 0.1 % 0.1 % 0.1 % Grindsted FF 1102 1.7% 1.7% 1.7% Egg yolk 1 4.23 % Egg yolk 2 4.23 % Egg yolk 3 4.23 % Vinegar 10% 4.00 % 4.00 % 4.00 % Mustard 1.50 % 1.50% 1.50% Sum 100 % 100% 100 % TLC-analysis: TLC analysis was carried out as described above.

Particle size determination in mayonnaise: 2.0 g mayonnaise sample was dissolved in 22.5 g 0.2% SDS and stirred for minimum 10 30 minutes at 300 rpm. The particle size distribution was then measured on a Malvern Mastersizer.

RESULTS For production of mayonnaise with enzyme-modified egg yolk, egg yolk from Sanofa 15 A/S was used. This egg yolk contained 8% salt (compared to 0% in egg yolk from DamEg). Initial trials (not shown) showed that the higher salt concentration in egg yolk from Sanofa A/S influenced the lipolytic activity and, therefore, an enzyme dosage of 30 U/g was used instead of 20 U/g.

TLC analysis of extracted lipid from enzyme modified egg yolk from Sanofa A/S (figure 29) showed that the lipolytic enzyme according to the present invention reduced the amount of lecithin concurrent with increasing the amount of lyso-lecithin 548497 119 (Figure 29). In comparison, the conversion of lecithin to lyso-lecithin when using Lecitase® Ultra was negligible. The high conversion of lecithin to lyso-lecithin shown by TLC correlated well with the free fatty acid determination made on extracted lipid from enzyme modified egg yolk from Sanofa A/S (Table 21). The amount of free fatty 5 acid liberated using lipolytic enzyme was 3.5 times higher than the amount of free fatty acid liberated using Lecitase® Ultra.

Table 21: Amount of free fatty acid in enzyme modified egg yolk from Sanofa A/S. The amount of free fatty acid was analysed by the NEFA.C method and is expressed as 10 percentage of egg yolk.

Sample Free fatty acid (% (w/w)) Control 0.39 Lipolytic enzyme 2.4 Lecitase® Ultra 0.68 The size distribution of oil droplets in mayonnaise was analysed in order to evaluate the emulsification properties of the differently enzyme-modified egg yolk from Sanofa A/S. As can be seen in, the mayonnaise produced with egg yolk treated with the 15 lipolytic enzyme according to the present invention had the smallest mean particle size as well as the narrowest particle size distribution compared to mayonnaise produced with either Lecitase® Ultra treated egg yolk or non- treated egg yolk. A small mean particle size as well as a narrow particle size distribution indicates good emulsification properties, hence the egg yolk modified with lipolytic enzyme had the best 20 emulsification properties.

Table 22: Particle size distribution in mayonnaise made with enzyme modified egg yolk from Sanofa A/S.

Sample Mean particle % quantile 90% quantile size (|rm) (ixm) (Hm) Control 13.7 2.0 21.5 Lipolytic enzyme 4.4 1.2 7.3 Lecitase® Ultra 13.3 1.8 21.9 548497 120 To evaluate the heat stability of emulsions made with enzyme modified egg yolk from Sanofa A/S, the mayonnaises were heated in a microwave oven for 4 seconds. As can be seen in Figure 30, the mayonnaises containing enzyme-modified egg yolk produced heat stable emulsions, whereas the control containing non-treated egg yolk separated 5 upon the heat treatment in the microwave oven and the emulsion was therefore not heat stable.

Conclusion Results from TLC analysis and free fatty acid determination of enzyme modified egg 10 yolk from Sanofa A/S, and particle size distribution and heat stability test of the mayonnaises produced with the enzyme modified egg yolk from Sanofa A/S correlated well. Egg yolk modified using a lipolytic enzyme according to the present invention had the highest conversion rate of lecithin to lyso-lecithin and the highest amount of free fatty acid. As expected, this change in the lecithin:lyso-lecithin ratio resulted in a 15 mayonnaise, which was heat stable and had the most optimal particle size distribution.

Using Lecitase® Ultra to modify egg yolk from Sanofa A/S did not result in a very large change in the lecithin:lyso-lecithin ratio or a high amount of free fatty acids. This less pronounced conversion of lecithin to lyso-lecithin was reflected in the particle size 20 distribution of the mayonnaise, which was similar to that of tlie non-modified egg yolk. The change in lecithin:lyso-lecithin ratio that occurred using Lecitase® Ultra was enough, though, to make the mayonnaise heat stable.

Egg yolk from Sanofa A/S modified with 30 U/g of lipolytic enzyme at 30°C for 120 25 minutes showed a high conversion rate of lecithin to lyso-lecithin, and the mayonnaise produced with this egg yolk was heat stable and had an optimal particle size distribution. In comparison, egg yolk from Sanofa A/S treated with 30 U/g Lecitase® Ultra at 30°C for 120 minutes showed only a minor change in the lecithin:lysolecithin ratio, and the mayonnaise produced had a particle size distribution similar to 30 mayonnaise with non-treated egg yolk, but it was in fact heat stable. Hence the 548497 121 lipolytic enzyme according to the present invention was superior to Lecitase® Ultra in the production of mayonnaise.

Example 11. Application test of a lipolytic enzyme derived from Fusarium 5 heterosporum in combination with emulsifier for preparation of hard crusty rolls.

In this test ferments of lipolytic enzyme according to the present invention and derived from Fusarium heterosporum was used alone or in combination with Panodan® A2020 DATEM and GRINDSTED® SSL P55, both emulsifiers from Danisco A/S, 10 for the baking of hard crusty rolls. The effect on specific bread volume was compared to the effect of Lipopan F™ from Novozymes alone or in combination with emulsifier on specific bread volume.

APPLICATION Hard crusty rolls were baked using the following recipe and baking procedure.

Baking recipe Amount Bakers % of flour Flour- Danish Reform 2004002 2000g 100 Compressed yeast Sugar Ascorbic acid Salt Water 1140 g 120 g 32 g 32 g 57 6 1.6 1.6 0 0 ppm Standard alpha amylase/GRINDAMYL™ A 1000 from Danisco A/S 75 ppm 0.150 Baking procedure Diosna mixer system 1. Dry mix for 1 min slow 2. Mix 2 min slow + 4 min fast 3. Dough temperature: 26°C 4. Scaling of the dough: 1350 g 548497 122 . Resting: 10 min. at 30°C in heating cabinet 6. Moulding: Fortuna 3/17/7 molder 7. Proofing: 45 min. at 34°C, 85% RH. 8. Baking in a Bago oven: 13 min. at 220°C, 13sec. steam + 5 min damper open 5 9. MIWE stone deck: prog, nr 1 . After baking the rolls are cooled for 25 min before weighing. The volume of the rolls was measured by the rape seed displacement method.

Specific bread volume: Specific volume = Volume of the bread, ccm/ weight of the bread, g Addition of spray dried lipolytic enzyme is based on flour. The enzyme is added to flour after first mixing together with water, ascorbic acid and compressed yeast. All other dry ingredients are mixed in step 1.

RESULTS Spray dried lipolytic enzyme derived from Fusarium heterosporum is used in combination with Panodan® M2020 DATEM from Danisco A/S and tested against a combination of Lipopan F™ / DATEM as well as pure Lipopan F™ or pure DATEM. The results are shown in Table 23 and Figure 31.

Table 23 Sample Control Lipopan F™ Amount Specific volume, g/ccm ,89 ppm 5,98 ppm 7,54 40 ppm 8,18 96 ppm 6,07 191 ppm 6,2 548497 123 Lipolytic enzyme 287 ppm 7,06 383 ppm 8,13 478 ppm 8,01 PAN M2020 0.3% 7,89 0.15% 6,5 PAN M2020 + 0.15% Lipolytic enzyme 96 ppm 7,68 PAN M2020 + 0.15% Lipolytic enzyme 191 ppm 8,29 PAN M2020 + 0.15% Lipopan F™ 10 ppm 7,69 Freeze dried lipolytic enzyme derived from Fusarium heterosporum was used in combination with Panodan® A2020 DATEM and GRINDSTED® SSL P55 and tested 5 against a combination of Lipopan F™ / SSL or Lipopan F™ / DATEM as well as pure Lipopan F™, pure DATEM and pure SSL.

The results are shown in Table 24 and Figure 32 Table 24 Sample Amount Specific volume, g/ccm Control 5,98 0,3% Panodan® A2020 0.3% 7.98 0,3% SSL P 55 0.3% 7.78 Lipopan F™ ppm 6.42 548497 Lipopan F™ + 0.15% Panodan® A2020 Lipopan F™ + 0.15% SSLP 55 Lipolytic enzyme Lipolytic en2yme + 0.15% Panodan® A2020 Lipolytic enzyme + 0.15% Panodan® A2020 Lipolytic enzyme + GRINDSTED® SSL P55 124 40 ppm 7.77 15 ppm 0.15% 8,44 15 ppm 0.15% 8,62 43 ppm 5,93 86 ppm 6,43 ppm 0.15% 7,86 43 ppm 0.15% 7,86 43 ppm 0.15% 8,1 CONCLUSION The conclusion of Table 23 and Figure 31 is that an optimal dosage of spray dried 5 lipolytic enzyme according to the present invention is approximately 383 ppm lipolytic enzyme and that the product can be used in a low dosage in combination with a low dosage of the DATEM emulsifier. In a parallel experiment it was shown that at dosages from 574 ppm to 1912 ppm lipolytic enzyme the specific bread volume decreased (data not shown). The performance of 383 ppm lipolytic enzyme according 10 to the present invention is similar to 40 ppm Lipopan F™. When used in combination with emulsifier the lipolytic enzyme according to the present invention also performs on level with Lipopan F™. According to determination of phospholipase activity using the TIPU assay described previously herein, 10 ppm Lipopan F™ is approx. 120 TIPU per kg flour and 96 ppm lipolytic enzyme of the present invention correspond to 117 15 TIPU per kg flour. 548497 125 In addition, based on the trial results of Table 24 and Figure 32, we conclude that a lipolytic enzyme according to the present invention can be used in combination with SSL as well as DATEM and thereby boost the effect of a low emulsifier level. The functionality of lipolytic enzyme according to the present invention can be compared 5 to the functionality of Lipopan F™ when dosed equally. Again the optimal level of phospholipase activity in combination with an emulsifier is determined to be approx. 100-150 TIPU per kg flour.

Conclusively, an optimal dosage of the pure lipolytic enzyme according to the present 10 invention is around 500 TIPU per kg flour and in combination with emulsifier the level of lipolytic enzyme should be 1/5 to Va of the optimal level of lipolytic enzyme, meaning approx. 120 TIPU per kg flour.

Example 12. Application test of a lipolytic enzyme derived from Fusarium heterosporum for preparation of wheat tortilla.

The effect of a lipolytic enzyme according to the present invention and derived from Fusarium heterosporum on reliability of wheat tortilla made with fumaric acid (US 20 procedure) has been tested as explained in the following example.

Wheat tortilla was baked using the ingredients in Table 25: Table 25: Recipe for preparation of wheat tortilla.

Recipe: Type: Dosage (% of flour) Grams Flour Classic (no. 200406B) 100 3000 Sugar 1,0 Fat (shortening, margarine, oil) Shortening 8,7 267 Salt 1,5 45 Potassium sorbate 0,3 9 Ca-propionate 0,3 9 Sodium bicarbonate 0,9 27 548497 126 Acid Fumaric 0,8 24 Water 48 144 The procedure for making the wheat tortilla dough: 1. Desired dough temperature: 32°C 2. Kneading is conducted at ambient temperature in a Kemper mixer. 3. Place all dry ingredients in mixer bowl (optionally including lipolytic enzymes and/or emulsifiers). 4. Dry mix for 1 min.

. Add Water 6. Mixing: 11 min at speed 1 7. Scaling: 1350 g x 3 8. Shaping: into dough balls on glimek divider / rounder 9. Resting for 10 min at 32°C . Baking: in a tortilla oven CFO 40, with the following setting: Top: 230°C, middle: 228°C and bottom: 160°C. 11. Cooling: 12 min at 20°C, 80% RH A lipolytic enzyme according to the present invention was added to the dough at increasing concentrations (Trial no. 3-7). For comparison, a control (Trial no. 1) and a trial with the Panodan® 205 emulsifier from Danisco A/S (Trial no. 2) were included. 20 See Table 26.

The lipolytic enzyme, Panodan® 205, and L-cystein, when added, are added to tlie first mixing process (steps 3 and 4 above). L-cystein may be added to increase the extensibility of the dough made and thereby improve the pressing process of the dough 25 before baking. 548497 127 Table 26. Trial set-up Ingredients Trial no.

Lipolytic enzyme PANODAN® 205 L'cystein (ppm) 1 2 1.03% 3 lOOpprn 4 200ppm 400ppm 6 1200ppm 7 2400ppm The tortillas are evaluated by means of a cold reliability test performed at room temperature, where the tortilla is rolled around different wooden sticks of different 5 diameters, starting with the wooden stick with the biggest diameter. The reliability is indicated by the number of wooden sticks around which the tortilla can be rolled without breaking. The higher the number the better the rollability.

Visual evaluation Penetration Sample Rollability Force (g) 1-day 7 2-1-1 432 2-day 7 1-1-1 421 3-day 7 1-1-1 369 4-day 7 2-2-2 439 -day 7 2-2-1 489 6-day 7 2-1-2 448 7-day 7 2-2-2 533 From the results we conclude that a dosage of 200 ppm or more of a lipolytic protein according to the present invention seems to give an improved rollability compared to the control system. Using the TEPU assay described previously herein it was determined that the level of activity needed in order to improve the rollability (in a dosage of 200 ppm) corresponds to approximately 650 TIPU units per kg flour. From 548497 128 the results it can also be concluded that the force for making the penetration test is increased at a higher level of lipolytic enzyme, meaning that the resistance of the tortilla is improved. The penetration test is conducted by use of the texture analyser TAXT2 produced by Stable Micro System, where the force needed in order to 5 penetrate/break the tortilla is measured.

This equipment is set up with the following parameters: Force is measured in Compression Pre-test Speed Test Speed Post Test Speed Rupture Test Dist. Distance 15 Force Time Load Cell Temperature lOmm/s 2 mra/s lOmm/s 1mm 25mm lg 5 sec 5kg -22 deg C (room temperature) Example 13. Molecular cloning, sequence analysis and heterologous expression of a synthetic gene encoding a lipolytic enzyme from Fusarium semitectum (IBT9507) in Hansenula polymorpha.

A fragment of a F. semitectum lipolytic enzyme gene was cloned from genomic DNA using PCR with primers designed from conserved blocks of amino acids within aligned protein sequences of lipolytic enzymes from different Fusarium strains. The degenerate PCR primers were designed using the computer programs CODEHOP (Rose et al. 30 2003(Nucleic Acid Res., 18:3763-3766)). 548497 129 To clone tlie ends of the gene the methods for 5- and 3'- RACE (Frohnian et al. 1988 Proc. Natl. Acad. Sci. USA 85:8998-9002) were used. Total RNA was isolated from a culture of the F. semitectum strain induced with 1% sunflower oil and the primers used were designed from the sequence of the gene fragment obtained with the CODEHOP primers.

The three fragments obtained by the above procedures were assembled in silico to reveal the full-length cDNA sequence. Analysis of the 1236 nucleotides long cDNA sequence showed an open reading frame comprising 352 amino acids (Figure 33).

To express the F. semitectum lipolytic enzyme gene in Hansenula the gene was furnished with a signal sequence form the yeast a mating factor and inserted behind the FMD-promoter into the Hansenula expression vector pB14. The resulting plasmid, pB14-alp.sem (schematically shown in Figure 34) was transformed into competent Hansenula polymorpha cells by electroporation. Transformants were selected on YND plates and 15 colonies were further selected for multiple integration of the gene by 10 passages of 1:200 dilutions in liquid cultures of YND. Finally, the selected cultures were transferred twice in YPD medium.

To determine the level of expression of the lipolytic enzyme gene the selected clones were 20 grown in YPD with 1.8% glycerol and 0.2% glucose for 2 days at 37°C.

Example 14. Determination of optimum pH and temperature for activity of a Fusarium semitectum lipolytic enzyme.

A lipolytic enzyme according to the present invention from Fusarium semitectum IBT 9507 and expressed in Hansenula polymorpha as described in Example 8 was used in functional assays in dough slurry for determination of phospholipase and galactolipase activity and the activity of this enzyme was studied in relation to variations in pH and temperature. 548497 130 ANALYTICAL PROCEDURES Gas Chromatography 0.8 gram Wheat flour is scaled in a 12 ml centrifuge tube with lid. 1.5 ml water containing 5 the enzyme is added. The sample is mixed on a Whirley and placed in a heating cabinet at 30°C for 60 minutes. 6 ml n-Butanol:Ethanol 9:1 is added, and the sample is mixed again until tlie flour is finely distributed in the solvent. The tubes are then placed in a water bath at 95°C for 10 minutes. Then, mixed again and placed on a rotation device 45 rpm, for 45 minutes. The sample is then centrifuged at 2000 g for 10 minutes and 2 ml supernatant is 10 transferred to a 10 ml dram glass. The solvent is evaporated at 70°C under a steam of nitrogen. The isolated lipids are analysed by GLC.

Gas Chromatograph and Galactolipase activity assay were performed as described in Example 1.

Temperature optimum Phospholipase activity For the determination of activity as a function of temperature the Phospholipase assay was conducted as in Example 1 but the temperature was set at 30°C, 37°C, 45°C, 52°C or 20 60°C. pH optimum Phospholipase activity For the determination of activity as a function of pH the Phospholipase assay was 25 conducted as in Example 1 but the 0.6% L-a Phosphatidylcholine 95% Plant (Avanti #441601) and 0.4% Triton-X 100 (Sigma X-100) was dissolved in 0.05M phosphate buffer pH 5, pH 6, pH 7, pH 8 or pH 9. 548497 131 RESULTS A lipolytic enzyme according to the present invention from Fusarium semitectum IBT9507 was analysed for phospholipase activity PLU-7 and galactolipase activity GLU with results shown in table 27 Table 27. Enzyme activity of Fusarium semitectum. Assay Activity Phospholipase Galactolipase 0,8 PLU-7/ml 1,3 GLU/ml Fusarium semitectum IBT9507 was tested in dough slurry experiments by adding 1 PLU-7 10 to 0.8 gram flour according to the procedure mentioned. A control sample with water instead of enzyme and a sample with Lipopan F™ was also prepared. Lipids extracted from the dough was analysed by GLC with results shown in table 28.

Table 28. GLC of dough lipid, % based on flour weight. FFA = free fatty acids MGMG = 15 monogalactosylmonoglyceride, DGMG = digalactosylmonoglyceride MGDG = monogalactosyldiglyceride. DGDG = digalactosyldiglyceride, TRI = triglyceride.

Enzyme Dosage FFA MGMG DGMG MGDG DGDG TRI % % % % % % Control 0 0,148 0,007 0,025 0,047 0,160 0,516 F. semitectum 1 PLU—7/g g flour 0,268 0,001 0,120 0,033 0,045 0,446 LipopanF™ 1 PLU—7/ggflour 0,229 0,027 0,090 0,016 0,069 0,415 The results in table 28 indicate that the lipase from F. semitectum has significant activity 20 on galactolipids, and relative less activity on triglyceride compared with Lipopan F™.

Fusarium semitectum IBT9507 was also analysed with regard to activity as a function of temperature (table 29) and pH (table 30), 548497 132 Table 29. Phospholipase activity as a function of temperature for F. semitectum.

Temperature, °C Relative activity, PLU 79 37 92 45 100 52 20 60 2 Table 30. Phospholipase activity as a function of pH for F. semitectum. pH Relative activity, PLU _ _ 6 83 7 100 8 80 9 17 The activities listed in table 29 and 30 are also illustrated graphically in Figures 35 and 36.

CONCLUSION Lipolytic enzyme according to the present invention from Fusarium semitectum has shown 10 very strong activity on galactolipids in dough and the activity on triglyceride is less than the triglyceride activity of Lipopan F™. Temperature optimum for activity of this enzyme is approx. 45°C and the pH optimum is 7.

Example 15; Use of a lipolytic enzyme according to the present invention in 15 animal feed To assess the efficacy of a lipolytic enzyme according to the present invention at various dose levels used in normal feed for the full production period of broiler chickens. 548497 133 Summary: Preliminary results suggest that addition of a lipolytic enzyme according to the present invention in the diets of broiler chickens is an effective nutritional strategy to improve 5 the performance of the birds, to improve nutrient retention and to reduce nitrogen excretion. Specifically, preliminary investigations suggest that addition of a lipolytic enzyme according to the present invention to the animal's diet improves the body weight gain, feed conversion efficiency, and metabolisability of dry matter and of nitrogen of the animal.

Treatment details Number of treatments 8 Replicates per Treatment 0-2Id, 13 replicates 22-42d, 9 replicates Birds per Replicate 0-2Id, 8 birds/replicate (6 in large cage, 2 in small cage) 22-42d, 2 birds/replicate (2 in large cage) Species of bird Broiler Breed of bird Ross or Cobb Sex of bird Male Range of trial 0-42 days Diet form (pellet/mash) Mash Diet Coccidiostat / Growth promoter used None Age at which birds / feed are weighed 0,21 and 42 days/ 0,21 and 42 days Stocking density (birds/m2) Lighting programme 23h light days 0-4, 16h light days 4-21, 20 h light days 22-31 and 23 h light days 32 -42.

House temperature programme House humidity programme 548497 134 Vaccination programme Elancoban (starter ration) Ventilation — Air changes/hr Diet formulation and feeding schedule Ingredients Starter (%) Finisher (%) Maize 55.55 59.22 Rye .00 9.00 SBM (48% CP) 33.47 24.79 Soy Oil 1.85 3.06 Salt 0.41 0.33 DL Methionine 0.21 0.14 Lysine HC1 0.05 0.10 Limestone 1.18 1.15 Dicalcium Phosphate 1.48 1.41 Vit/Min 0.50 0.50 Ti02 0.30 0.30 TOTAL 100.00 100.00 Nutrient Provision (calculated) CP (%) 21.50 18.06 .

ME (keal/kg) 3000.0 3125.0 ME (MJ/kg) 12.55 13.08 Calcium (%) 0.90 0.85 Phos(%) 0.68 0.63 Av. Phos (%) 0.40 0.38 Fat (%) 4.48 .73 Fibre (%) 2.59 2.48 Met (%) 0.55 0.43 Cys (%) 0.36 0.32 Met+Cys (%) 0.91 0.75 548497 135 Lys (%) Try (%) 1.20 1.00 0.25 0.20 Na (%) 0.18 0.15 The feed is prepared as a mash, either with or without a lipolytic enzyme according to the present invention.

Diets and water are offered ad libitum. Test diets are fed continuously throughout the trial period. The feed samples are optionally supplemented with a lipolytic enzyme according to tlie present invention at 330g/tonne. The enzyme may be added as a dry enzyme whilst mixing the feed.

Observations are taken at: Live weight (cage basis): day 0,21 and 42 FCR (food conversion rate): 0-21 d, 22-42d, 0-42days Collection of ileal contents: day 21 and 42 Total cage weights for feed and birds are determined, as well as total mortality weight and number of birds for each cage per period analysed.- Feed consumption per cage is 20 determined uncorrected for mortality. Feed conversion efficiency data is determined as total consumption per live weight and total weight (including mortality weight) basis.

Prior to the study start the animals are examined for signs of ill health and injury. Any 25 that appear to be in poor condition are removed from the study.

Weight gain: Feed Intake: 0-2Id, 22-42d, 0-42days 0-21 d, 22-42d, 0-42days Study animals are assigned to their treatment groups using a randomisation technique. Animals and their storage pens are uniquely identified before the start of administration of test feed. 548497 WO 2005/087918 PCT/IB2005/000875 136 Data from the treated groups are compared with those of their relevant control group using the appropriate statistical tests and accepting a level of probability of less than 0.05 as indicating significance.

Body weights, food intakes and food conversion rates are analysed by analysis of variance and least significant difference tests.

Animals Treatment Number : 2 Number of replicates : 13 to 21 days and 9 to 42 days Animals per replicate : 8 to 21 days and 2 to 42 days Species of Animal : Broiler Breed of animal : Ross Sex : Male Age of test animals : 0-42d Weights of test animals : ~40g Diet/Housing 20 Diet Information Diet Form Coccidiostat Starter Coccidiostat Finisher Growth Promoter Starter 25 Growth Promoter Finisher See above Mash None None None None Main Measurements made Variables : weight gain, feed conversion, nutrient digestibility When : 0-2Id, 22-42d WO 2005/087918 PCT/IB2005/000875 137 Enzymes/additives Enzymes used (1) : Lipolytic enzyme from Fusarium semitectum and/or Fusarium heterosporum - 330g/Tonne Example 16: Evaluation of the effect of a Fusarium heterosporum CBS 782.83 lipolytic enzyme on instant noodle quality made from Chinese flour.

Introduction The instant noodle (IN) market has seen a phenomenal growth in the last 5-8 years in SE 10 Asia, and to some extent in Europe and USA. This growth is evident even in regions that are traditionally rice and/or pasta based markets (Food Navigator, 2000). The recent popularity of IN can be mainly attributed to its very affordable cost, convenience and clean production procedures.

Flour with an average protein content (9-11%), low ash value (-0.50%), high L* (85) brightness and b* (>8.0) yellowness and high starch paste viscosity (<750 BU) produces a creamy/yellow coloured instant noodle (IN) and has the desired mouth feel characteristics. There are several different types of noodles consumed, each with specific flour quality characteristics that impact on end product quality.

Meeting end user demands is challenging in the flour industry owing to the large number of end products and wide range of customer expectations. Specifically designed ingredients and additives at the right doses play a very important role in improving taste, texture, appearance, shelf life and/or nutritive value of the final end product Whilst the importance of colour and texture of cooked IN cannot be underestimated, customers are getting increasingly discerning and health conscious and are seeking low fat alternatives without compromising on quality. 548497 138 A lipolytic enzyme according to the present invention was tested on Chinese flour in order to evaluate the effect on fat content of IN and study the changes to texture and colour during processing.

Materials and Methods The standard Agrifood Technology procedure for IN production and an extended evaluation method was used for this project. Chinese flour was used as the control flour and was run at the start of each day. The protein content, moisture, ash, colour, 10 wet gluten and diastatic activity of the Chinese flour were measured using AACC (American Association for Clinical Chemistry) approved methods. Dough rheology tests included: farinogram, extensogram (45 min pull), alveogram and amylogram.

The IN production can be summarized as follows: Each batch of IN was made from 350 g flour and mixed at low speed during which 33 parts of aqueous salt solution containing 1% sodium chloride and 0.2% alkaline salts (potassium carbonate: sodium carbonate in the ratio 6:4) was gradually added. For dosed samples, the flour was mixed thoroughly with the measured amount of 20 ingredient prior to the addition of the aqueous salty solution.

The crumbly dough was mixed for a further 4 minutes at medium speed and sheeted 8 times. Sheeting commenced with a steel compactor, followed by two plastic fluted rollers and finally by five stainless steel smooth rollers, with a 30% reduction ratio 25 between each roll. The final dough sheet thickness was 1.35 mm. The dough sheet was sheeted once more prior to cutting. The differential in speed between the cutting rolls and the conveyor belt resulted in tight curls being formed. The tightly curled noodle strands were steamed for two minutes, fried in palm oil on both sides at 180°C for 1 minute. The noodle blocks were cooled and packed in clip seal bags for further 30 analyses. 548497 139 Samples were collected at several stages of production for analyses. The colour and particle size of the crumb were measured using the Minolta Chromameter and the vernier calipers, respectively. The colour of the dough sheet and the final product were recorded with the Minolta Chromameter and a digital photo was taken of both (not 5 shown). Water activity measurements were conducted on the steamed noodles. Water activity may be measured by determining the weight of the steamed noodles, both immediately after steaming and after complete removal of water content by drying in an oven at 90°C - the water content can then be determined by dividing the weight difference before and after drying by the weight after drying.

Optimal cooking time, cooking yield, cooking losses (gravimetric method), colour and texture (firmness) of cooked noodles were measured using standard Agrifood Technology procedures known to a person skilled in the art. Texture profile analysis (TPA) was also conducted on cooked noodle texture in order to measure cohesiveness, 15 springiness and chewiness.

Cohesiveness is defined as how well the product withstands a second deformation relative to how it behaved under the first deformation. It is measured as tlie area of work during the second compression divided by the area of work during the first 20 compression and hence has no units of measurements. Cohesiveness, in this instance relates to product 'al-dente', which is not a desirable attribute for IN.

Springiness is defined as how well a product physically springs back after it has been deformed during the first compression. Springiness is measured in several ways, but 25 most typically, by the distance of the detected height of the product on the second compression.

Chewiness only applies to solid products, and is calculated as gumminess multiplied by springiness. Chewiness is mutually exclusive with gumminess. 548497 140 One noodle block representing each dosage rate was ground in a coffee grinder and a homogenous sub sample was used for fat analysis by acid hydrolysis method (alternative standard methods for determining fat content may be used).

Results and Discussion The protein content and colour (with respect to brightness, L*) of the flour was within the acceptable range for the production of instant noodles. The water absorption was slightly on the higher end for IN production; however, as the noodle dough is quite crumbly it did not impact machinability.

The flour had good single (extensogram) and bi-axial (alvcogram) extensibility, which would have a positive impact on the eating qualities of the noodle. Peak viscosity of the amylograph was 870 BU, which is desirable for IN.

Cooking loss of IN containing the second highest dose of lipolytic enzyme was higher than the control and the IN containing the least amount of the lipolytic enzyme according to the present invention. The fat content of IN with the highest amount of the lipolytic enzyme was significantly lower than the control and the experimental IN with the lowest amount of lipolytic enzyme. Springiness and chewiness of some 20 experimental IN were better than the control. Based on this data, the lipolytic enzyme should be investigated further at different dosages.

Conclusions Some of the salient points that can be made from this study are: The addition to IN of a lipolytic enzyme according to the present invention did not dramatically impact on crumb size, dough stickiness, machinability or processing characteristics. Importantly, increasing dosages of lipolytic enzyme resulted in a 30 reduction in fat content of IN. Lipolytic enzyme improved noodle firmness at 548497 141 increasing doses compared to control while cohesiveness was not affected. Lipolytic enzyme had a positive effect on yellowness of cooked noodles.

Thus, lipolytic enzyme reduced fat content in IN, improved texture and increased 5 yellowness of cooked noodles.

All publications mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described methods and system of the present invention will be apparent to those skilled in the art without departing from the scope and 10 spirit of the present invention. Although the present invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in biochemistry and biotechnology or related fields are intended to 15 be within the scope of the following claims. 5W$37

Claims (17)

WHAT WE CLAIM IS:

1. A fungal lipolytic enzyme wherein the enzyme comprises an amino acid sequence as shown in SEQ ID No. 1 or SEQ ID No. 2 or SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity to any one of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 4 or SEQ ID No. 6.

2. A fungal lipolytic enzyme according to claim 1 wherein the enzyme is obtained from a filamentous fungus

3. A fungal lipolytic enzyme according to claim 1 or claim 2 wherein the enzyme is obtained from Fusarium spp.

4. A fungal lipolytic enzyme according to claim 3, wherein the enzyme is obtained from Fusarium heterosporum.

5. A nucleotide sequence encoding a fungal lipolytic enzyme according to any one of claims 1-5.

6. A nucleic acid encoding a fungal lipolytic enzyme, which nucleic acid is selected from the group consisting of: a) a nucleic acid comprising a nucleotide sequence shown in SEQ ID No. 3 or SEQ ID No. 5 or SEQ ID No. 7; b) a nucleic acid which is related to the nucleotide sequence of SEQ ID No. 3 or SEQ ID No. 5 or SEQ ID No. 7 by the degeneration of the genetic code; and c) a nucleic acid comprising a nucleotide sequence which has at least 90% identity with the nucleotide sequence shown in SEQ ID No. 3 or SEQ ID No. 5 or SEQ ID No. 7.

7. A method of making a foodstuff comprising adding the fungal lipolytic enzyme according to any one of claims 1-4 or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to one or more ingredients of the foodstuff. #6062462 RFCEIVEt 1 6 SEP 2MB ^f$t97

8. A method of making a baked product comprising adding a fungal lipolytic enzyme according to any one of claims 1-4 or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to a dough and baking the dough to make the baked product.

9. A method according to claim 7 wherein the foodstuff is one or more of: egg or an egg-based product; a baked product; confectionery; a frozen product; a dairy product including a cheese; a mousse; a whipped vegetable cream; an edible oil and fat; an aerated and non-aerated whipped product; an oil-in-water emulsions and water-in-oil emulsions; margarine; shortening; a spread, including low fat and very low fat spreads; a dressing; mayonnaise; a dip; a cream based sauce; a cream based soup; a beverage; a spice emulsion and a sauce.

10. A method according to any one of claim 7-9, wherein the lipolytic enzyme is used in combination with an alpha-amylase.

11. A method of preparing a lyso-phospholipid comprising treating a phospholipid with the fungal lipolytic enzyme according to any one of claims 1-4 or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to produce the lyso-phospholipid.

12. A method of preparing a lyso-glycolipid comprising treating a glycolipid with a fungal lipolytic enzyme according to any one of claims 1 -4 or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides to produce a lyso-glycolipid.

13. A method of enzymatic degumming of vegetable or edible oils, comprising treating the edible or vegetable oil with a fungal lipolytic enzyme according to any one of claims 1-4 or a fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides so as to hydrolyse a major part of the polar lipids present therein.

14. A method according to any one of claims 7-13 wherein the enzyme has a phospholipid:triglyceride hydrolysing activity ratio of at least 4. #6062462 intellectual property OFFICE OF N Z. 1 6 SEP 2009 RECEIVED RECEIVED at IPONZ on 25 November 2009 548497 144

15. A foodstuff obtained by the method according to claim 7 or 9.

16. A baked product obtained by the method of claim 8.

17. A bread improving composition or dough improving composition comprising the fungal lipolytic enzyme according to any one of claims 1-4 and an alpha-amylase. 2294033_l.doc