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CN108185422A - A kind of relieving alcoholism and protecting liver type fig ferment and preparation method thereof - Google Patents

A kind of relieving alcoholism and protecting liver type fig ferment and preparation method thereof Download PDF

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CN108185422A
CN108185422A CN201810122547.7A CN201810122547A CN108185422A CN 108185422 A CN108185422 A CN 108185422A CN 201810122547 A CN201810122547 A CN 201810122547A CN 108185422 A CN108185422 A CN 108185422A
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fermentation
preparation
enzyme
liver
ferment
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夏其乐
陈剑兵
曹艳
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Zhejiang Academy of Agricultural Sciences
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/065Microorganisms
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus
    • A23V2400/123Bulgaricus
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus
    • A23V2400/169Plantarum
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/21Streptococcus, lactococcus
    • A23V2400/249Thermophilus

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  • Health & Medical Sciences (AREA)
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  • Polymers & Plastics (AREA)
  • Mycology (AREA)
  • Microbiology (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

本发明涉及农产品加工技术领域,具体涉及一种解酒护肝型无花果酵素及其制备方法,所述方法包括如下步骤:(1)原料破碎:将无花果鲜果破碎打浆,得到无花果果浆;(2)加糖调整:按照无花果果浆的量添加白砂糖,搅拌均匀;(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌接入步骤(2)中得到的无花果果浆中,恒温静置,该过程保持密闭状态;(4)通气、后发酵:步(3)得到的无花果果浆经发酵后,通入洁净空气,并充分搅拌,随后密封发酵容器,再静置,即得到无花果酵素原液。利用该制备方法得到的无花果酵素具有解酒护肝功效。

The present invention relates to the technical field of agricultural product processing, in particular to a hangover-protecting liver-protecting fig enzyme and a preparation method thereof. The method comprises the following steps: (1) crushing raw materials: crushing and beating fresh fig fruits to obtain fig pulp; (2) ) sugaring adjustment: add white granulated sugar according to the amount of fig pulp, and stir evenly; (3) add strains to ferment: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the fig pulp obtained in step (2) (4) aeration and post-fermentation: After the fig pulp obtained in step (3) is fermented, it is fed into clean air and fully stirred, then the fermentation container is sealed, and then left to stand , to obtain the fig enzyme stock solution. The fig enzyme obtained by the preparation method has the effect of relieving alcohol and protecting the liver.

Description

一种解酒护肝型无花果酵素及其制备方法A kind of anti-alcoholic and liver-protecting fig enzyme and preparation method thereof

技术领域technical field

本发明涉及农产品加工技术领域,具体涉及一种解酒护肝型无花果酵素及其制备方法。The invention relates to the technical field of agricultural product processing, in particular to a hangover-protecting liver-protecting fig enzyme and a preparation method thereof.

背景技术Background technique

无花果(Ficuscarica L.)属桑科(Moraceae)无花果属(Ficus L.)植物,原产于亚洲西南部和地中海东部地区,现在广泛种植于地中海的大多数国家和美国的加利福尼亚,大约在1000多年前传入我国。无花果栽培利用历史悠久,但是整体面积和产量不大,因此专家学者把它与蓝莓等浆果一起列入“第三代水果”的范畴,具有极其广阔的发展空间。无花果可食率高,鲜果可食用部分达97%,且含酸量低,无大而坚硬的种子,适宜老人和儿童食用。无花果除含有较高的单糖和二糖外,还含有果胶等多糖,具有较好的生理活性。果实中含有18种氨基酸,其中8种是人体必需氨基酸。无花果富含黄酮、多糖、SOD等具有防治心血管疾病和老年性痴呆症的生理活性物质,也含有抗癌功能的呋喃香豆素、补骨酯素、佛手柑内酯等物质。现代医学研究表明无花果有增强机体免疫功能和抑制多种肿瘤细胞增殖的作用,还具有降血糖、降低血胆固醇和抗蠕虫的功效。Fig (Ficuscarica L.) is a plant of the genus Ficus (Ficus L.) of the family Moraceae. It is native to southwestern Asia and the eastern Mediterranean region. It is now widely planted in most countries in the Mediterranean Sea and California in the United States for about 1,000 years. forward into our country. Figs have a long history of cultivation and utilization, but the overall area and output are not large. Therefore, experts and scholars include them in the category of "third-generation fruits" together with blueberries and other berries, and have extremely broad development space. The edible rate of figs is high, the edible part of the fresh fruit is up to 97%, and the acid content is low, without large and hard seeds, suitable for the elderly and children. In addition to high monosaccharides and disaccharides, figs also contain polysaccharides such as pectin, which have good physiological activities. The fruit contains 18 kinds of amino acids, 8 of which are essential amino acids for human body. Figs are rich in flavonoids, polysaccharides, SOD and other physiologically active substances that can prevent and treat cardiovascular diseases and Alzheimer's disease, and also contain anti-cancer substances such as furanocoumarin, psoralen, and bergamot lactone. Modern medical research shows that figs can enhance the immune function of the body and inhibit the proliferation of various tumor cells, and also have the effects of lowering blood sugar, lowering blood cholesterol and resisting worms.

由于无花果果皮非常薄,且成熟于炎热的夏秋季节,加之现阶段的贮藏技术和冷链有限等因素,无花果极易腐烂。随着人们对无花果营养价值认识的不断深入,社会需求也越来越多,无花果国内消费市场前景广阔,故发展无花果种植业潜力巨大。但无花果鲜果成熟衰老快、易腐烂、保存性差,贮藏、运输困难,因地制宜的开展无花果加工技术的研究与产业化示范具有重要的意义。酵素是经过微生物发酵制得的新型发酵饮品,在实现纯天然绿色食品呈递以及功能化增值等方面具有卓越的表现。按照团体标准《酵素产品分类导则》(T/CBFIA 08001-2016)的定义,酵素是以动物、植物、菌类等为原料,经微生物发酵制得的含有特定生物活性成分的产品,无花果由于含糖量高,且多糖所占的比例高,加热后无异味,非常适合微生物的生长利用,是生产酵素的良好原料。Because the skin of figs is very thin and matures in the hot summer and autumn seasons, coupled with factors such as the current storage technology and limited cold chain, figs are extremely perishable. With the continuous deepening of people's understanding of the nutritional value of figs, the social demand is also increasing, and the domestic consumption market of figs has broad prospects, so the development of fig planting industry has great potential. However, fresh figs ripen quickly, are perishable, have poor preservation, and are difficult to store and transport. It is of great significance to carry out research and industrialization demonstration of fig processing technology according to local conditions. Enzyme is a new type of fermented drink made by microbial fermentation, which has excellent performance in the realization of pure natural green food presentation and functional value-added. According to the definition of the group standard "Guidelines for the Classification of Enzyme Products" (T/CBFIA 08001-2016), enzymes are products containing specific biologically active ingredients made from animals, plants, fungi, etc., through microbial fermentation. The sugar content is high, and the proportion of polysaccharides is high, and there is no peculiar smell after heating. It is very suitable for the growth and utilization of microorganisms, and is a good raw material for the production of enzymes.

无花果鲜果发酵生产酵素,能够形成新的优良风味,并有效保持其天然的营养成分。与国内外现有的无花果加工方法相比,微生物发酵法制备的无花果发酵饮料的独特的优点包括:(1)与传统罐装、糖渍果蔬以及果蔬酱料相比,它的含糖量可以降低80%,更符合当前低糖健康饮食理念;(2)与干制果蔬(粉)相比,它能够更好的保持新鲜果蔬的营养成分;(3)与鲜切果蔬相比,它具有更长的货架周期,和更平缓的果蔬产量消耗压力。因此进行无花果酵素的研究与产业化示范既符合果蔬加工发展的趋势,满足消费者对健康产品的追求,也能够增加产地无花果的消耗量,减少果农的损失,具有很好的经济效益和社会效益。Fresh figs are fermented to produce enzymes, which can form new and excellent flavors and effectively maintain their natural nutrients. Compared with existing fig processing methods at home and abroad, the unique advantages of the fig fermented beverage prepared by microbial fermentation include: (1) compared with traditional canned, candied fruits and vegetables and fruit and vegetable sauces, its sugar content can It is more in line with the current concept of low-sugar healthy diet; (2) Compared with dried fruits and vegetables (powder), it can better maintain the nutritional content of fresh fruits and vegetables; (3) Compared with fresh-cut fruits and vegetables, it has more Long shelf life, and more gentle consumption pressure of fruit and vegetable production. Therefore, the research and industrialization demonstration of fig enzyme is not only in line with the development trend of fruit and vegetable processing, satisfying consumers' pursuit of healthy products, but also can increase the consumption of figs in the production area, reduce the loss of fruit farmers, and has good economic and social benefits. .

化学性肝损伤,是由化学性肝毒性物质所造成的肝损伤,这些化学物质包括酒精、环境中的化学毒物及某些药物。酒精性肝病根据不同病情可分为酒精性肝脂肪变性、酒精性肝炎、酒精性肝纤维化、酒精性肝硬化:酒精性肝脂肪变性是良性可逆的,酒精性肝炎可发生肝细胞坏死,其5年存活率为60%,而重症酒精性肝炎如不及时治疗,则49%病人可于几个月内死亡,酒精性肝纤维化是组织坏死的结果,常导致肝硬化。在慢性嗜酒者中约有30%发展成肝硬化。目前对酒精性肝硬化尚无特效疗法,5年存活率仅为50%,且有10%的肝硬化者可演变为肝癌。Chemical liver injury is liver injury caused by chemical hepatotoxic substances, including alcohol, chemical poisons in the environment, and certain drugs. Alcoholic liver disease can be divided into alcoholic liver steatosis, alcoholic hepatitis, alcoholic liver fibrosis, and alcoholic liver cirrhosis according to different conditions: alcoholic liver steatosis is benign and reversible, and alcoholic hepatitis can cause liver cell necrosis. The 5-year survival rate is 60%. If severe alcoholic hepatitis is not treated in time, 49% of patients will die within a few months. Alcoholic liver fibrosis is the result of tissue necrosis, often leading to liver cirrhosis. About 30% of chronic alcoholics develop cirrhosis. Currently there is no specific therapy for alcoholic liver cirrhosis, the 5-year survival rate is only 50%, and 10% of patients with liver cirrhosis can evolve into liver cancer.

申请号201510036161.0的发明专利申请,发明名称为一种制备无花果乳酸混菌发酵功能饮料的方法,将无花果酶解、121℃下灭菌20分钟得到无花果发酵准备液,随后将植物乳杆菌、嗜热链球菌和保加利亚乳杆菌以1:1:1的质量比接入上述的葛根(本发明人理解此处应为无花果)发酵准备液,随后进行发酵。为了保持无花果较高的营养成分的优良的风味,无花果发酵前必须进行高温灭菌处理,因此所述发明专利申请提供的方法需要将无花果高温灭菌后再接菌发酵,这样就不存在有害微生物生长繁殖的可能。但是经过灭菌处理后的无花果酵素解酒护肝功效差,因此为了得到解酒护肝功效优良的无花果酵素有必要研究新的制备工艺。The invention patent application with the application number 201510036161.0, the title of the invention is a method for preparing a fig lactic acid mixed bacteria fermented functional beverage. The fig is enzymatically hydrolyzed and sterilized at 121°C for 20 minutes to obtain a fig fermentation preparation liquid, and then Lactobacillus plantarum, thermophilic Streptococcus and Lactobacillus bulgaricus were inserted into the above-mentioned kudzu root (the inventor understands that it should be fig here) fermentation preparation solution with a mass ratio of 1:1:1, and then fermented. In order to maintain the excellent flavor of the higher nutritional content of figs, high-temperature sterilization must be carried out before fermentation of figs. Therefore, the method provided by the patent application for the invention requires high-temperature sterilization of figs before inoculation and fermentation, so that there will be no harmful microorganisms The possibility of growth and reproduction. However, the anti-alcohol and liver-protecting effect of fig enzyme after sterilization is poor, so it is necessary to study a new preparation process in order to obtain the fig enzyme with excellent anti-alcohol and liver-protecting effect.

发明内容Contents of the invention

本发明的目的充分利用鲜销剩余的无花果鲜果,利用现代菌种发酵,制得具有解酒护肝能力的无花果酵素产品,符合广大消费者追求健康食品的理念。The purpose of the present invention is to make full use of the remaining fresh figs from fresh sales and ferment them with modern strains to produce fig enzyme products with the ability to relieve alcohol and protect the liver, which is in line with the concept of consumers pursuing healthy food.

为实现本发明的发明目的,发明人提供如下技术方案:In order to realize the purpose of the invention of the present invention, the inventor provides the following technical solutions:

一种解酒护肝型无花果酵素的制备方法,按以下步骤进行:A preparation method for hangover-protecting liver-protecting fig enzyme, carried out according to the following steps:

(1)原料破碎:将无花果鲜果破碎打浆,得到无花果果浆;(1) Crushing of raw materials: crushing and beating fresh figs to obtain fig pulp;

(2)加糖调整:按照无花果果浆的量添加白砂糖,搅拌均匀;(2) Adjustment by adding sugar: add white granulated sugar according to the amount of fig pulp, and stir evenly;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌接入步骤(2)中得到的无花果果浆中,恒温静置,该过程保持密闭状态;(3) Add strains to ferment: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the fig pulp obtained in step (2), leave it at a constant temperature, and keep the process in an airtight state;

(4)通气、后发酵:步(3)得到的无花果果浆经发酵后,通入洁净空气,并充分搅拌,随后密封发酵容器,再静置,即得到无花果酵素原液。(4) Ventilation and post-fermentation: After the fig pulp obtained in step (3) is fermented, clean air is introduced and fully stirred, then the fermentation container is sealed, and then left to stand to obtain the fig enzyme stock solution.

优选的,步骤(2)中,白砂糖的加入量为无花果果浆质量的10%-30%。Preferably, in step (2), the amount of added white granulated sugar is 10%-30% of the mass of fig pulp.

在该比例条件下:发酵得到的无花果酵素具有更为显著的解酒护肝功效。Under the condition of this ratio: the fermented fig enzyme has a more significant anti-alcohol and liver-protecting effect.

优选的,步骤(3)中,所述植物乳杆菌、保加利亚乳杆菌和嗜热链球菌质量比为:2:1:1。植物乳杆菌、保加利亚乳杆菌和嗜热链球菌都是应用广泛的乳酸菌,复合使用除了能够产生酸外,还能形成优良的风味。申请号201510036161.0的发明专利申请制备无花果乳酸混菌发酵功能饮料虽然也是采用植物乳杆菌、保加利亚乳杆菌和嗜热链球菌,三个菌种的比例是1:1:1,为了保持无花果较高的营养成分的优良的风味,无花果发酵前必须进行高温灭菌处理,因此申请号201510036161.0的发明专利申请提供的方法需要将无花果高温灭菌后再接菌发酵,这样就不存在有害微生物生长繁殖的可能。而利用本发明的技术方案,虽然省去无花果发酵前必须进行的高温灭菌处理步骤,试验证明不但依然能够有效抑制霉菌、酵母等生长繁殖,而且保持了无花果较高的营养成分的优良的风味,并且在动物模型试验中,本发明提供的方法制备得到的无花果酵素相较于申请号201510036161.0的发明专利申请具有更为优异的解酒护肝功效。Preferably, in step (3), the mass ratio of the Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus is 2:1:1. Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus are widely used lactic acid bacteria, and combined use can not only produce acid, but also form excellent flavor. The invention patent application number 201510036161.0 is applied for the preparation of fig lactic acid mixed bacteria fermented functional beverage. Although Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus are also used, the ratio of the three strains is 1:1:1. For the excellent flavor of nutrients, figs must be subjected to high-temperature sterilization before fermentation. Therefore, the method provided by the invention patent application with application number 201510036161.0 requires high-temperature sterilization of figs before inoculation and fermentation, so that there is no possibility of growth and reproduction of harmful microorganisms . And utilizing the technical scheme of the present invention, although the high-temperature sterilization treatment step that must be carried out before fig fermentation is omitted, the test proves that not only can still effectively inhibit the growth and reproduction of mold, yeast, etc., but also maintain the excellent local flavor of figs with higher nutritional components. , and in animal model tests, the fig enzyme prepared by the method provided by the present invention has a more excellent anti-alcohol and liver-protecting effect than the invention patent application with application number 201510036161.0.

优选的,步骤(3)中,所述恒温温度为20-25℃,静置时间为10-15d。Preferably, in step (3), the constant temperature is 20-25°C, and the standing time is 10-15d.

经过试验验证植物乳杆菌、保加利亚乳杆菌和嗜热链球菌在20-25℃温度范围内可以稳定生长,设定发酵温度为20-25℃可以减少企业的设备投入。前期初步试验表明,在20-25℃的条件下,密闭条件下发酵10-15d后,体系中的产酸量维持在稳定的水平上。It has been verified by experiments that Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus can grow stably in the temperature range of 20-25°C. Setting the fermentation temperature at 20-25°C can reduce the equipment investment of enterprises. Preliminary experiments showed that after 10-15 days of fermentation under airtight conditions at 20-25°C, the acid production in the system remained at a stable level.

优选的,步骤(4)中,发酵时间为15-20d,搅拌时间为30-60min,静置时间为30d。Preferably, in step (4), the fermentation time is 15-20d, the stirring time is 30-60min, and the standing time is 30d.

根据发酵容器的大小,一般通气30-60min即可使前期发酵产生的不良气味溢出,也可以达到充分搅拌无花果果浆的作用。再次静置发酵30d后即达到了平衡状态,时间再增加,产酸量也无法提高。According to the size of the fermentation container, generally ventilating for 30-60 minutes can make the bad smell produced by the early fermentation overflow, and can also achieve the effect of fully stirring the fig pulp. The equilibrium state was reached after 30 days of static fermentation again, and the amount of acid production could not be increased if the time was increased.

一种解酒护肝型无花果酵素的制备方法,按以下步骤进行:A preparation method for hangover-protecting liver-protecting fig enzyme, carried out according to the following steps:

(1)原料破碎:将无花果鲜果用水清洗并沥干,用打浆机破碎打浆,得到无花果果浆;(1) Crushing of raw materials: washing the fresh figs with water and draining, crushing and beating with a beater to obtain fig pulp;

(2)加糖调整:按照无花果果浆的质量添加10%-30%的白砂糖,搅拌均匀;(2) sugaring adjustment: add 10%-30% white granulated sugar according to the quality of fig pulp, stir evenly;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以2:1:1的质量比接入上述的无花果果浆中,于20-25℃的条件下恒温静置10-15d,该过程保持密闭状态;(3) Fermentation by adding strains: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the above-mentioned fig pulp at a mass ratio of 2:1:1, and let it stand at a constant temperature at 20-25°C 10-15d, the process remains airtight;

(4)通气、后发酵:无花果果浆经15-20d发酵后,通入洁净空气,并充分搅拌,该过程持续30-60min,随后密封发酵容器,再静置30d后,即得到无花果酵素原液。(4) Ventilation and post-fermentation: after the fig pulp is fermented for 15-20 days, it is introduced into clean air and fully stirred. The process lasts for 30-60 minutes, and then the fermentation container is sealed, and after standing for 30 days, the fig enzyme stock solution is obtained .

利用该优选工艺生产的无花果酵素具有显著的解酒护肝功效,并且有减轻肝脏重量与脏器系数,提高球蛋白,降低白蛋白,降低总胆红素,促进乙醇脱氢酶与乙醛脱氢酶分泌的作用,并对酒精性脂肪肝有一定的保护作用。The fig ferment produced by this optimal process has a significant anti-alcoholic and liver-protecting effect, and can reduce liver weight and organ coefficient, increase globulin, reduce albumin, reduce total bilirubin, and promote the dehydrogenation of alcohol dehydrogenase and acetaldehyde. Hydrogenase secretion, and has a certain protective effect on alcoholic fatty liver.

另一方面,本发明提供了一种利用上述方法制备得到的无花果酵素。In another aspect, the present invention provides a fig enzyme prepared by the above method.

再一方面,本发明提供了一种利用上述方法制备得到的无花果酵素在解酒护肝方面的用途。In another aspect, the present invention provides a use of the fig ferment prepared by the above method in hangover and liver protection.

本发明的有益效果是:The beneficial effects of the present invention are:

1.利用鲜销剩余的无花果或者品相较差的果实,采用间歇通气法生产无花果酵素,避免了因无花果大量腐烂而伤农的情况;1. Use the remaining figs sold fresh or the fruits of poor quality, and use the intermittent aeration method to produce fig enzymes, avoiding the situation that farmers are injured due to a large number of rotten figs;

2.该工艺生产的无花果酵素具有显著的解酒护肝功效,对于保护嗜酒人士的健康具有重要的作用。2. The fig enzyme produced by this process has a significant anti-alcoholic and liver-protecting effect, and plays an important role in protecting the health of alcoholics.

附图说明Description of drawings

图1为正常组肝脏×400倍电镜图;Figure 1 is an electron micrograph of the liver in the normal group × 400 times;

图2为模型组肝细胞×400倍电镜图;Figure 2 is an electron micrograph of model group liver cells × 400 times;

图3为无花果低剂量组×400倍电镜图;Fig. 3 is the fig low-dose group × 400 times electron micrograph;

图4为无花果高剂量组×400倍电镜图。Fig. 4 is an electron micrograph of the fig high-dose group × 400 times.

具体实施方式Detailed ways

下面结合实施例,更具体地说明本发明的内容。应当理解,本发明的实施并不局限于下面的实施例,对本发明所做的任何形式上的变通和/或改变都将落入本发明保护范围。Below in conjunction with embodiment, the content of the present invention is described more specifically. It should be understood that the implementation of the present invention is not limited to the following examples, and any modifications and/or changes made to the present invention will fall within the protection scope of the present invention.

在本发明中,若非特指,所有的份、百分比均为重量单位,所有的设备和原料等均可从市场购得或是本行业常用的。若无特别指明,实施例采用的方法为本领域通用技术。In the present invention, unless otherwise specified, all parts and percentages are weight units, and all equipment and raw materials can be purchased from the market or commonly used in this industry. Unless otherwise specified, the methods used in the examples are common techniques in the art.

主要原料和设备说明:Description of main raw materials and equipment:

本发明的蓝莓采摘自浙江宁波,品种“玛斯义陶芬”。The blueberry of the present invention is picked from Ningbo, Zhejiang, and the variety is "Masiyi Taofen".

打浆机:DS-1型,上海标本模型厂;Beater: DS-1 type, Shanghai Specimen Model Factory;

植物乳杆菌、保加利亚乳杆菌、嗜热链球菌,均为市售。Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus are commercially available.

实施例1Example 1

一种解酒护肝型无花果酵素及其制备方法,按以下步骤进行:A hangover-protecting liver-protecting fig enzyme and a preparation method thereof, the steps are as follows:

(1)原料准备:无花果鲜果经水清洗、沥干后破碎打浆;(1) Raw material preparation: fresh figs are washed with water, drained, and then crushed and beaten;

(2)加糖调整:按步骤(1)得到的无花果果浆的量添加10%的白砂糖,搅拌均匀;(2) sugaring adjustment: add 10% white granulated sugar according to the amount of fig pulp obtained in step (1), stir evenly;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以2:1:1的质量比接入上述的无花果果浆中,于20℃的条件下恒温静置10d,该过程保持密闭状态;(3) Fermentation by adding strains: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the above-mentioned fig pulp at a mass ratio of 2:1:1, and let it stand at a constant temperature for 10 days at 20°C. The process remains airtight;

(4)通气、后发酵:无花果果浆经10d发酵后,通入洁净空气,并充分搅拌,该过程持续30min,随后密封发酵容器,再静置30d后,即得到无花果酵素原液。(4) Ventilation and post-fermentation: After 10 days of fermentation of the fig pulp, clean air was introduced and fully stirred. The process lasted for 30 minutes, and then the fermentation container was sealed, and after standing still for 30 days, the fig enzyme stock solution was obtained.

实施例2(产品定义为高植物乳杆菌型酵素,简称HLP酵素)Embodiment 2 (the product is defined as the high lactobacillus plantarum type ferment, referred to as HLP ferment)

一种解酒护肝型无花果酵素及其制备方法,按以下步骤进行:A hangover-protecting liver-protecting fig enzyme and a preparation method thereof, the steps are as follows:

(1)原料准备:无花果鲜果经水清洗、沥干后破碎打浆;(1) Raw material preparation: fresh figs are washed with water, drained, and then crushed and beaten;

(2)加糖调整:按步骤(1)得到的无花果果浆的量添加10%的白砂糖,搅拌均匀;(2) sugaring adjustment: add 10% white granulated sugar according to the amount of fig pulp obtained in step (1), stir evenly;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以3:1:1的质量比接入上述的无花果果浆中,于20℃的条件下恒温静置10d,该过程保持密闭状态;(3) Fermentation by adding strains: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the above-mentioned fig pulp at a mass ratio of 3:1:1, and let it stand at a constant temperature for 10 days at 20°C. The process remains airtight;

(4)通气、后发酵:无花果果浆经10d发酵后,通入洁净空气,并充分搅拌,该过程持续30min,随后密封发酵容器,再静置30d后,即得到无花果酵素原液。(4) Ventilation and post-fermentation: After 10 days of fermentation of the fig pulp, clean air was introduced and fully stirred. The process lasted for 30 minutes, and then the fermentation container was sealed, and after standing still for 30 days, the fig enzyme stock solution was obtained.

对照实施例1Comparative Example 1

一种解酒护肝型无花果酵素及其制备方法,按以下步骤进行:A hangover-protecting liver-protecting fig enzyme and a preparation method thereof, the steps are as follows:

(1)原料准备:无花果鲜果经水清洗、沥干后破碎打浆;(1) Raw material preparation: fresh figs are washed with water, drained, and then crushed and beaten;

(2)加糖调整:按步骤(1)得到的无花果果浆的量添加10%的白砂糖,搅拌均匀;(2) sugaring adjustment: add 10% white granulated sugar according to the amount of fig pulp obtained in step (1), stir evenly;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以1:1:1的质量比接入上述的无花果果浆中,于20℃的条件下恒温静置10d,该过程保持密闭状态;10d的密闭发酵期结束后,通入洁净空气置换容器中气体的过程中,闻到一阵水果的腐败外溢出,表明有害微生物繁殖差生了异味,不符合食用植物酵素标准。因此植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以1:1:1的方案不可行。(3) Fermentation by adding strains: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into the above-mentioned fig pulp at a mass ratio of 1:1:1, and let it stand at a constant temperature for 10 days at 20°C. The process was kept in a closed state; after the 10d closed fermentation period, during the process of introducing clean air to replace the gas in the container, there was a burst of fruit corruption, which indicated that the harmful microorganisms had poor reproduction and produced peculiar smells, which did not meet the edible plant enzyme standard. Therefore, a 1:1:1 ratio of Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus is not feasible.

对照实施例2(产品定义为高温灭菌型酵素,简称HT酵素)Comparative Example 2 (the product is defined as a high temperature sterilization type ferment, referred to as HT ferment)

一种解酒护肝型无花果酵素及其制备方法,按以下步骤进行:A hangover-protecting liver-protecting fig enzyme and a preparation method thereof, the steps are as follows:

(1)原料准备:无花果鲜果经水清洗、沥干后破碎打浆;(1) Raw material preparation: fresh figs are washed with water, drained, and then crushed and beaten;

(2)加糖调整:按步骤(1)得到的无花果果浆的量添加10%的白砂糖,搅拌均匀,将无花果果浆121℃下灭菌20分钟;(2) Adjustment by adding sugar: add 10% white granulated sugar to the amount of fig pulp obtained in step (1), stir evenly, and sterilize the fig pulp at 121°C for 20 minutes;

(3)添加菌种发酵:将植物乳杆菌、保加利亚乳杆菌和嗜热链球菌以2:1:1的质量比接入经过高温灭菌的无花果果浆中,于20℃的条件下恒温静置10d,该过程保持密闭状态;(3) Fermentation by adding strains: insert Lactobacillus plantarum, Lactobacillus bulgaricus and Streptococcus thermophilus into high-temperature sterilized fig pulp at a mass ratio of 2:1:1, and keep the temperature at 20°C. Set 10d, the process remains airtight;

(4)通气、后发酵:无花果果浆经10d发酵后,通入洁净空气,并充分搅拌,该过程持续30min,随后密封发酵容器,再静置30d后,即得到无花果酵素原液。(4) Ventilation and post-fermentation: After 10 days of fermentation of the fig pulp, clean air was introduced and fully stirred. The process lasted for 30 minutes, and then the fermentation container was sealed, and after standing still for 30 days, the fig enzyme stock solution was obtained.

实施例3:功能测试Example 3: Functional Test

1.防醉解酒功能测试1. Anti-drunk hangover function test

采用56度北京二锅头酒一次性灌胃法建立小鼠醉酒模型,以研究无花果酵素的解酒作用。小鼠于给酒前和给酒后分别灌胃,给予样品低、高剂量,观察其对急性乙醇醉酒的影响。A mouse model of drunkenness was established by one-time gavage of Beijing Erguotou wine at 56 degrees to study the anti-alcoholic effect of fig enzyme. Mice were gavaged before and after drinking, and given low and high doses of samples, and observed their effects on acute ethanol intoxication.

(1)受试药物与试剂(1) Test drugs and reagents

样品无花果酵素由浙江省农业科学院提供,高、低剂量分别配制成0.5g/mL和0.25g/mL溶液待用;“千杯不醉”解酒胶囊(浙江省诸暨市朝阳路78号);56度北京二锅头酒(北京红星股份有限公司,产品标准:GB/T10781.2)。The sample fig enzyme was provided by the Zhejiang Academy of Agricultural Sciences, and the high and low doses were prepared into 0.5g/mL and 0.25g/mL solutions for use; 56% Beijing Erguotou Liquor (Beijing Red Star Co., Ltd., product standard: GB/T10781.2).

(2)试验动物(2) Test animals

ICR小鼠130只,体重18-22g,性别雄性。由上海斯莱克实验动物有限责任公司提供,生产许可证:SCXK(浙)2014-0001。饲养条件:检验过程在屏障系统实验室中完成(空气洁净度≤1万级,空气换气次数10~20次/小时,温度20~26℃,日温差≤3℃,相对湿度40%-70%),使用许可证:SYXK2012-0178。小鼠饲喂60Co灭菌的大小鼠生长繁殖饲料,由上海斯莱克实验动物有限责任公司提供,沪饲审(2014)04001。自由饮食饮水,笼器具、垫料等均经121℃高压灭菌,消毒20分钟。130 ICR mice, body weight 18-22g, sex male. Provided by Shanghai Slack Experimental Animal Co., Ltd., production license: SCXK (Zhejiang) 2014-0001. Breeding conditions: The inspection process is completed in a barrier system laboratory (air cleanliness ≤ 10,000, air ventilation times 10-20 times/hour, temperature 20-26°C, daily temperature difference ≤3°C, relative humidity 40%-70°C %), use license: SYXK2012-0178. Mice were fed 60Co sterilized rat growth and reproduction feed, provided by Shanghai Slack Experimental Animal Co., Ltd., Shanghai Feed Review (2014) 04001. Free to eat and drink, cage utensils, bedding, etc. were all sterilized by autoclaving at 121°C for 20 minutes.

(3)灌胃酒量的选择(3) Choice of alcohol intake

取小鼠50只,随机分为5组,每组10只,禁食12h后,各组分别按比例(酒量:体重)灌胃56度北京二锅头酒0.10、0.15、0.16、0.18、0.20mL/10g,观察令小鼠翻正反射消失但无死亡的所需酒量。50 mice were randomly divided into 5 groups, 10 in each group. After fasting for 12 hours, each group was given 0.10, 0.15, 0.16, 0.18, 0.20 mL/ 10g, observe the amount of alcohol needed to make the mouse righting reflex disappear but without death.

(4)样品防醉试验(4) Sample anti-drunk test

取雄性小鼠40只,随机分为4组,每组10只,分别为模型组、阳性对照组(““千杯不醉”解酒胶囊”0.4g/KG)、样品低剂量组(2.5g/kg)、样品高剂量组((5.0g/kg)。各组小鼠以标准饲料喂养,自由饮水,适应性喂养1周后进行试验。试验前各组小鼠禁食12h,各组给药容积10mL/KG,模型对照组灌胃给予等量的饮用水,样品组和阳性对照组分别灌胃相应的供试液。15min后,各组均以0.18mL/10g的酒量灌56度北京二锅头酒。观察小鼠灌酒后的情况,记录小鼠翻正反射消失的时间和恢复时间,计算出耐受时间和醉酒时间。Get 40 male mice and divide them into 4 groups at random, 10 in each group, respectively model group, positive control group ("Qianbei Buzui" hangover capsule" 0.4g/KG), sample low dose group (2.5 g/kg), sample high-dose group ((5.0g/kg). The mice in each group were fed with standard feed, drank water freely, and carried out the test after adaptive feeding for 1 week. Before the test, the mice in each group were fasted for 12h, and the mice in each group were fasted for 12 hours. The volume of administration was 10mL/KG, the model control group was given the same amount of drinking water by intragastric administration, and the sample group and the positive control group were given the corresponding test solution by intragastric administration. After 15 minutes, each group was administered with 0.18mL/10g alcohol volume of 56 degrees Beijing Erguotou wine. Observe the situation of the mice after drinking, record the time of disappearance of the righting reflex and the recovery time of the mice, and calculate the tolerance time and drunken time.

(5)样品解酒试验(5) Sample hangover test

动物分组与适应性饲养同前,试验前,各组小鼠禁食12h,先以0.16mL/10g的酒量灌胃56度北京二锅头酒,15min后,模型对照组灌胃给予饮用水,阳性对照组和样品组分别灌胃相应的供试液,各组给药容积10mL/KG。观察小鼠灌酒后的情况,记录小鼠翻正反射消失的时间(醉酒时间)和恢复时间(醒酒时间),计算出耐受时间和维持时间。Animal grouping and adaptive feeding were the same as before. Before the test, the mice in each group were fasted for 12 hours, and 56% Beijing Erguotou wine was given to the stomach with 0.16mL/10g of alcohol. After 15 minutes, the model control group was given drinking water. The test group and the sample group were given the corresponding test solution respectively, and the administration volume of each group was 10mL/KG. Observe the situation of the mice after drinking, record the time when the righting reflex disappears (drunk time) and the recovery time (sober time) of the mice, and calculate the tolerance time and maintenance time.

(6)统计方法(6) Statistical method

计量资料以“均数±标准差”(M+SD)表示。用SPSS V17.0统计软件包进行方差齐性检验及t检验。The measurement data are expressed as "mean ± standard deviation" (M+SD). The homogeneity of variance test and t test were performed with SPSS V17.0 statistical software package.

2.保肝护肝功能测试2. Liver protection function test

采用56度北京二锅头酒灌胃一周,建立小鼠急性肝损伤模型,以研究无花果酵素和保肝作用。小鼠每天于给药前灌胃二锅头酒12ml/kg/d,给酒后30min分别给予无花果酵素低、高剂量,观察其对急性肝损伤的保护作用。A mouse model of acute liver injury was established by intragastric administration of 56-degree Beijing Erguotou wine for one week to study fig enzymes and hepatoprotective effects. The mice were fed with Erguotou wine 12ml/kg/d every day before administration, and were given low and high doses of fig enzyme 30 minutes after drinking to observe its protective effect on acute liver injury.

(1)受试材料与试剂(1) Test materials and reagents

无花果酵素由浙江省农业科学院提供,高、低剂量分别配制成0.5g/mL和0.25g/mL溶液待用;56度北京二锅头酒(北京红星股份有限公司,产品标准:GB/T10781.2)。ELISA试剂盒采购自上海朗顿生物科技有限公司。Fig enzyme is provided by Zhejiang Academy of Agricultural Sciences, and the high and low doses are prepared into 0.5g/mL and 0.25g/mL solutions respectively for use; 56 degrees Beijing Erguotou wine (Beijing Red Star Co., Ltd., product standard: GB/T10781.2) . The ELISA kit was purchased from Shanghai Longton Biotechnology Co., Ltd.

(2)仪器(2) Instrument

罗氏cobas 8000全自动生化仪,thermo公司varioskan flash酶标仪,LeicaEG1150H包埋机,Leica RM 2235石蜡切片机,Leica HI1220烤片机,Leica HI1210摊片机,Leica ASP300脱水机,Leica ST 5010全自动染色机。olympus CX21型显微镜。Roche cobas 8000 automatic biochemical analyzer, thermo company varioskan flash microplate reader, Leica EG1150H embedding machine, Leica RM 2235 paraffin slicer, Leica HI1220 roasting machine, Leica HI1210 spreading machine, Leica ASP300 dehydrator, Leica ST 5010 automatic dyeing machine. olympus CX21 microscope.

(3)试验动物(3) Test animals

ICR小鼠60只,体重25-27g,性别雄性。由上海斯莱克实验动物有限责任公司提供,生产许可证:SCXK(浙)2014-0001。饲养条件:检验过程在屏障系统实验室中完成(空气洁净度≤1万级,空气换气次数10-20次/小时,温度20~26℃,日温差≤3℃,相对湿度40%-70%),使用许可证:SYXK2012-0178。小鼠饲喂60Co灭菌的大小鼠生长繁殖饲料,由上海斯莱克实验动物有限责任公司提供,沪饲审(2014)04001。自由饮食饮水,笼器具、垫料等均经121℃高压灭菌,消毒20分钟。60 ICR mice, weighing 25-27g, are male. Provided by Shanghai Slack Experimental Animal Co., Ltd., production license: SCXK (Zhejiang) 2014-0001. Breeding conditions: The inspection process is completed in the barrier system laboratory (air cleanliness ≤ 10,000, air exchange rate 10-20 times/hour, temperature 20-26 °C, daily temperature difference ≤ 3 °C, relative humidity 40%-70 %), use license: SYXK2012-0178. Mice were fed 60Co sterilized rat growth and reproduction feed, provided by Shanghai Slack Experimental Animal Co., Ltd., Shanghai Feed Review (2014) 04001. Free to eat and drink, cage utensils, bedding, etc. were all sterilized by autoclaving at 121°C for 20 minutes.

(4)取样(4) Sampling

取小鼠40只,随机分为4组,分别为正常对照组、模型组、无花果酵素高剂量组、无花果酵素低剂量组,每组10只,每天按照12ml/kg/天的剂量灌胃52°红星二锅头,灌酒后30min无花果酵分别灌胃给药,实验周期一周,一周后,小鼠禁食12h,采血离心取上清,测ALT、AST、TP、ALB、总胆红素和乙醇脱氢酶、乙醛脱氢酶,动物解剖取肝脏,测量肝脏系数,并进行HE染色,观察肝损伤情况。40 mice were randomly divided into 4 groups, namely normal control group, model group, high-dose fig enzyme group, and low-dose fig enzyme group, with 10 mice in each group, and 52 ml/kg/day of oral administration per day. °Red Star Erguotou, 30 minutes after drinking, fig yeast was administered orally respectively, the experimental period was one week, after one week, the mice were fasted for 12 hours, the blood was collected and centrifuged to get the supernatant, and the ALT, AST, TP, ALB, total bilirubin and ethanol were measured For dehydrogenase and acetaldehyde dehydrogenase, the animal was dissected to take the liver, measure the liver coefficient, and perform HE staining to observe the liver damage.

(5)统计方法(5) Statistical methods

计量资料以“均数±标准差”(M+SD)表示。用SPSS V17.0统计软件包进行方差齐性检验及t检验。The measurement data are expressed as "mean ± standard deviation" (M+SD). The homogeneity of variance test and t test were performed with SPSS V17.0 statistical software package.

经动物试验证明,无花果酵素可以明显延长小鼠翻正反射消失时间(P<0.01),显著缩短醉酒时间(P<0.05);醉酒小鼠给予样品后,显著缩短了醉酒时间(P<0.01或P<0.05)。防醉试验中,HLP酵素高剂量组能够显著缩短小鼠的醉酒时间(P<0.05),HLP酵素低剂量组能够显著延长小鼠的耐受时间(P<0.05),但是都分别低于同样剂量的无花果酵素;解酒试验中,HLP酵素高剂量组能够显著延长小鼠的耐受时间(P<0.05),但是低于同样剂量的无花果酵素;HT酵素无论是防醉作用还是解酒作用都与模型组都无显著差异,即HT酵素无防醉解酒作用。试验表明无花果酵素具有良好的防醉解酒作用,且并非植物乳杆菌的用量越高其效果越好。无花果酵素有减轻肝脏重量与脏器系数,提高球蛋白,降低白蛋白,降低总胆红素,促进乙醇脱氢酶与乙醛脱氢酶分泌的作用,并对酒精性脂肪肝有一定的保护作用。试验结果见表1-5。Animal experiments have proved that fig enzyme can significantly prolong the disappearance time of righting reflex in mice (P<0.01), and significantly shorten the time of drunkenness (P<0.05); after giving samples to drunken mice, the time of drunkenness can be significantly shortened (P<0.01 or P<0.05). In the anti-drunk test, the high-dose HLP enzyme group can significantly shorten the drunk time of the mice (P<0.05), and the low-dose HLP enzyme group can significantly prolong the tolerance time of the mice (P<0.05), but they are all lower than the same In the hangover test, the high-dose HLP enzyme group can significantly prolong the tolerance time of mice (P<0.05), but it is lower than that of the same dose of fig enzyme; HT enzyme has the effect of anti-drunkness and hangover effect There is no significant difference with the model group, that is, HT enzyme has no anti-drunk and hangover effect. Tests have shown that fig enzyme has a good anti-drunk and hangover effect, and the higher the dosage of Lactobacillus plantarum, the better the effect. Fig enzyme can reduce liver weight and organ coefficient, increase globulin, reduce albumin, reduce total bilirubin, promote the secretion of alcohol dehydrogenase and acetaldehyde dehydrogenase, and have certain protection against alcoholic fatty liver effect. The test results are shown in Table 1-5.

表1无花果酵素对ICR小鼠的防醉作用Table 1 Anti-drunk effect of fig enzyme on ICR mice

*示与模型组比较有显著差异(P<0.05),**示与模型组比较有显著差异(P<0.01)* indicates a significant difference compared with the model group (P<0.05), ** indicates a significant difference compared with the model group (P<0.01)

表2无花果酵素对ICR小鼠的解酒作用Table 2 The anti-alcoholic effect of fig enzyme on ICR mice

*示与模型组比较有显著差异(P<0.05),**示与模型组比较有显著差异(P<0.01)* indicates a significant difference compared with the model group (P<0.05), ** indicates a significant difference compared with the model group (P<0.01)

根据表1和表2实验数据可以证实无花果酵素可以明显延长小鼠翻正反射消失时间(P<0.01),显著缩短醉酒时间(P<0.05);醉酒小鼠给予样品后,显著缩短了醉酒时间(P<0.01或P<0.05),说明无花果酵素具有良好的防醉解酒作用。According to the experimental data in Table 1 and Table 2, it can be confirmed that fig enzyme can significantly prolong the disappearance time of righting reflex in mice (P<0.01), and significantly shorten the time of drunkenness (P<0.05); after giving samples to drunken mice, the time of drunkenness can be significantly shortened (P<0.01 or P<0.05), indicating that the fig enzyme has a good anti-drunk and hangover effect.

表3无花果酵素对ICR小鼠体重及肝脏系数的影响Table 3 Effect of fig enzyme on body weight and liver coefficient of ICR mice

*示与模型组比较有显著差异(P<0.05)**示与模型组比较有显著差异(P<0.01)。*Indicates a significant difference compared with the model group (P<0.05) **Indicates a significant difference compared with the model group (P<0.01).

根据表3实验数据可以证实造模各组小鼠肝脏重均低于正常组,给药各组肝脏重低于模型组,其中无花果低剂量组与模型组比较有显著性差异(P<0.05),肝脏脏器系数与模型组相比显著降低,其中无花果低剂量组P<0.05,无花果高剂量组P<0.01。According to the experimental data in Table 3, it can be confirmed that the weight of the liver of mice in each group of modeling is lower than that of the normal group, and the weight of liver in each group of drug administration is lower than that of the model group, and there is a significant difference between the low-dose fig group and the model group (P<0.05) , The organ coefficient of the liver was significantly lower than that of the model group, among which the low-dose fig group was P<0.05, and the high-dose fig group was P<0.01.

表4无花果酵素对ICR小鼠血液生化指标的影响Table 4 The effect of fig enzyme on the blood biochemical indicators of ICR mice

Δ示与正常组比较有显著差异(P<0.05),*示与模型组比较有显著差异(P<0.05)**示与模型组比较有显著差异(P<0.01)。Δ indicates a significant difference compared with the normal group (P<0.05), * indicates a significant difference compared with the model group (P<0.05) ** indicates a significant difference compared with the model group (P<0.01).

根据表4实验数据可以证实模型组球蛋白显著降低,白蛋白显著升高(P<0.05),无花果酵素有提高球蛋白,降低白蛋白,降低总胆红素的作用。According to the experimental data in Table 4, it can be confirmed that the globulin in the model group is significantly reduced, and the albumin is significantly increased (P<0.05). Fig enzyme has the effects of increasing globulin, reducing albumin, and reducing total bilirubin.

表5无花果酵素对ICR小鼠乙醇脱氢酶、乙醛脱氢酶的影响Table 5 The effect of fig ferment on alcohol dehydrogenase and acetaldehyde dehydrogenase in ICR mice

ΔΔ示与正常组比较有显著差异(P<0.01),**示与模型组比较有显著差异(P<0.01)。ΔΔ indicates a significant difference compared with the normal group (P<0.01), ** indicates a significant difference compared with the model group (P<0.01).

根据表5实验数据可以证实造模能够诱导机体乙醇脱氢酶与乙醛脱氢酶显著升高,无花果高剂量组的乙醛脱氢酶较模型组显著升高(P<0.01)。According to the experimental data in Table 5, it can be confirmed that modeling can induce a significant increase in alcohol dehydrogenase and acetaldehyde dehydrogenase in the body, and the acetaldehyde dehydrogenase in the high-dose fig group is significantly higher than that in the model group (P<0.01).

另外从图1-4可以看出,正常组肝脏肝索结构完整,无脂肪空洞与炎性浸润,与正常组比较,模型组肝细胞弥漫性脂变,肝细胞肿胀变形、胞质浑浊,有网状结构,少数核固缩,出现炎性浸润,与模型组比较,无花果酵素组脂肪空洞减少,肝索结构明显,肿胀减轻。In addition, it can be seen from Figures 1-4 that the hepatic cord structure in the normal group was intact, without fat cavities and inflammatory infiltration. Reticular structure, a few nuclear pyknosis, and inflammatory infiltration appeared. Compared with the model group, the fat cavity in the fig enzyme group was reduced, the hepatic cord structure was obvious, and the swelling was reduced.

Claims (10)

1. a kind of preparation method of relieving alcoholism and protecting liver type fig ferment, carries out according to the following steps:
Step (1) raw material crushes:By fig fresh fruit crushing and beating, fig fruit latex is obtained;
Step (2) sugaring adjusts:White granulated sugar is added according to the amount of fig fruit latex, is stirred evenly;
Step (3) adds strain fermentation:It will be in lactobacillus plantarum, lactobacillus bulgaricus and streptococcus thermophilus access step (2) In obtained fig fruit latex, constant temperature is stood, which keeps air-tight state;
Step (4) ventilation, rear fermentation:After step (3) obtained fig fruit latex is fermented, pure air is passed through, and be sufficiently stirred, Container is then sealed by fermentation, then is stood to get to fig enzyme stoste.
2. preparation method according to claim 1, in the step (2), the additive amount of white granulated sugar is fig fruit latex matter The 10%-30% of amount.
3. preparation method according to claim 1, in the step (3), the lactobacillus plantarum, lactobacillus bulgaricus It is with streptococcus thermophilus mass ratio:2:1:1.
4. preparation method according to claim 1, in the step (3), the thermostat temperature is 20-25 DEG C, during standing Between be 10-15d.
5. preparation method according to claim 1, in step (4), fermentation time 15-20d, mixing time 30- 60min, time of repose 30d.
6. preparation method according to claim 1 carries out according to the following steps:
Step (1) raw material crushes:Fig fresh fruit is washed with water and drained, with beater crushing and beating, obtains fig fruit Slurry;
Step (2) sugaring adjusts:According to the white granulated sugar of the amount addition 10%-30% of fig fruit latex, stir evenly;
Step (3) adds strain fermentation:By lactobacillus plantarum, lactobacillus bulgaricus and streptococcus thermophilus with 2:1:1 quality Than accessing in above-mentioned fig fruit latex, constant temperature stands 10-15d under conditions of 20-25 DEG C, which keeps air-tight state;
Step (4) ventilation, rear fermentation:Fig fruit latex is passed through pure air, and be sufficiently stirred after 15-20d ferments, the mistake Cheng Chixu 30-60min are then sealed by fermentation container, then stand after 30d to get to fig enzyme stoste.
7. a kind of fig ferment being prepared using claim 1-6 any claims.
8. purposes of the fig ferment in terms of relieving alcoholism and protecting liver described in claim 7.
9. the fig ferment described in claim 7 is mitigating liver weight and organ coefficient, globulin is improved, reduces white egg In vain, the purposes in terms of total bilirubin, promotion alcohol dehydrogenase or promotion acetaldehyde dehydrogenase secretion is reduced.
10. the purposes in fig ferment protection alcoholic fatty liver described in claim 7.
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CN113817565A (en) * 2021-10-27 2021-12-21 中华全国供销合作总社济南果品研究院 Method for producing fig wine by combining lactic acid bacteria and saccharomyces cerevisiae fermentation
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