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14 pages, 3010 KiB  
Article
Surface Display of Multiple Metal-Binding Domains in Deinococcus radiodurans Alleviates Cadmium and Lead Toxicity in Rice
by Liangyan Wang, Yudong Wang, Shang Dai and Binqiang Wang
Int. J. Mol. Sci. 2024, 25(23), 12570; https://doi.org/10.3390/ijms252312570 - 22 Nov 2024
Viewed by 286
Abstract
Cadmium (Cd) and lead (Pb) are the primary hazardous heavy metals that accumulate in crops and pose substantial risks to public health via the food chain. Limiting the migration of these toxic metals from contaminated environments to rice is the most direct and [...] Read more.
Cadmium (Cd) and lead (Pb) are the primary hazardous heavy metals that accumulate in crops and pose substantial risks to public health via the food chain. Limiting the migration of these toxic metals from contaminated environments to rice is the most direct and crucial remediation approach. Bioremediation with microorganisms has been extensively utilized for managing heavy metal contamination in the natural environment, and the interplay between microbes and crops is important to alleviate heavy metal stress. Here, we express Lpp-OmpA fused with two metal-binding domains (PbBD and MTT5) in the outer membrane of Deinococcus radiodurans to enhance both Cd and Pb adsorption. Our results showed that the recombinant strain LOPM, which displayed an increased tolerance to both Cd and Pb stress, exhibited a 4.9-fold higher Cd adsorption and 3.2-fold higher Pb adsorption compared to wild-type strain R1. After LOPM cells colonized the rice root, Cd content reduced to 47.0% in root and 43.4% in shoot; Pb content reduced to 55.4% in root and 26.9% in shoot, as compared to the plant’s exposure to Cd and Pb. In addition, cells of LOPM strain colonized on rice roots alleviate Cd- and Pb-induced oxidative stress by reducing ROS levels and enhancing antioxidant enzyme activities in rice. This study supplies a promising application of genetic-engineering extremophile bacteria in reducing heavy metal accumulation and toxicity in rice. Full article
(This article belongs to the Special Issue Physiology and Molecular Biology of Plant Stress Tolerance)
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Figure 1
<p>Surface display of multiple metal-binding domains in <span class="html-italic">Deinococcus radiodurans</span> by gene fusion expression. (<b>A</b>) Schematic diagram of fusion protein module. LOMP stands for the fusion protein composed of Lpp-OmpA, PbBD and MTT5. (<b>B</b>) The structure of fusion protein LOPM is predicted by Alphafold 2. The circular area containing reducing cysteine (shown as yellow stick) is the close-up view of the region indicated by the arrow, respectively. (<b>C</b>) Scanning electron microscopy (SEM) and transmission electron micrograph (TEM) analyses of <span class="html-italic">D. raiodurans</span> wild-type strain R1 and recombinant strain LOPM. (<b>D</b>) Localization of LOPM using fluorescence labeling analysis. Scale bars = 2 μm. (<b>E</b>) Effect of Cd and Pb on the growth of <span class="html-italic">D. radiodurans</span> wild-type strain R1 and recombinant strain LOPM. Bacterial growth was observed under different concentrations of Cd and Pb.</p>
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<p>The total amount of Cd and Pb absorbed by the <span class="html-italic">D. radiodurans</span> wild-type strain R1 and recombinant strain LOPM. The three different treatments with medium containing 100 μM Cd (<b>A</b>), 200 μM Pb (<b>B</b>) and 100 μM Cd and 200 μM Pb (<b>C</b>), respectively. Cell morphology of <span class="html-italic">D. raiodurans</span> wild-type strain R1 and recombinant strain LOPM using SEM (<b>D</b>) and TEM (<b>E</b>). (<b>F</b>–<b>H</b>) Cd and Pb removal rates of <span class="html-italic">D. raiodurans</span> wild-type strain R1 and recombinant strain LOPM in medium containing 100 μM Cd (<b>F</b>), 200 μM Pb (<b>G</b>) and 100 μM Cd and 200 μM Pb (<b>H</b>), respectively.</p>
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<p>Impact of <span class="html-italic">D. radiodurans</span> supplementation on rice seedlings under cadmium and lead stress (Cd and Pb). Scale bar = 5 cm. Data were shown in mean ± SD with 20 (<b>A</b>–<b>C</b>) and 3 (<b>D</b>) repeats. Different letters indicate the significant differences with <span class="html-italic">p</span> ˂ 0.05. Medium compositions: Control: 0 μM CdCl<sub>2</sub> and 0 μM PbCl<sub>2</sub>; Cd and Pb: 100 μM CdCl<sub>2</sub> + 200 μM PbCl<sub>2</sub>; Cd and Pb + R1: 100 μM CdCl<sub>2</sub>, 200 μM PbCl<sub>2</sub> and <span class="html-italic">D. radiodurans</span> wild-type strain R1; Cd and Pb + LOMP: 100 μM CdCl<sub>2</sub>, 200 μM PbCl<sub>2</sub> and recombinant <span class="html-italic">D. radiodurans</span> strain LOPM.</p>
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<p>Fluorescence labeling (<b>A</b>) and SEM (<b>B</b>) analysis on root colonization of <span class="html-italic">D. radiodurans</span> wild-type strain R1 and recombinant strain LOPM. The rice root tissue co-cultured with colonized bacterial cells was observed by laser scanning confocal microscopy. The bacterial cell membrane was stained by Dil (red fluorescence). The colonized bacteria cells on the roots were indicated by the white arrows, scale bar = 1 mm.</p>
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<p>The content of cadmium (Cd) and lead (Pb) in the roots and shoots of rice plants after 10 days of growth with different treatments (<b>A</b>–<b>D</b>). The analyses were performed with three replications. The significant difference (<span class="html-italic">p</span> ˂ 0.05) was indicated by the different letters above the error bars. The details of different supplements were illustrated in <a href="#ijms-25-12570-f003" class="html-fig">Figure 3</a>.</p>
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<p>Accumulation of H<sub>2</sub>O<sub>2</sub>, malondialdehyde (MDA), and proline (Pro) in rice plants after 10 days of growth with different treatments. The accumulations of H<sub>2</sub>O<sub>2</sub> (<b>A</b>), MDA (<b>B</b>), and Pro (<b>C</b>) in roots and leaves. The significant difference (<span class="html-italic">p</span> &lt; 0.05) was indicated by the different letters above the error bars. The details of different supplements were illustrated in <a href="#ijms-25-12570-f003" class="html-fig">Figure 3</a>.</p>
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<p>CAT, POD, and SOD activities in rice plants after 10 days of growth with different treatments. The CAT (<b>A</b>), POD (<b>B</b>), and SOD (<b>C</b>) activities were detected in roots and leaves. The significant difference (<span class="html-italic">p</span> ˂ 0.05) was indicated by the different letters above the error bars. The details of different supplements were illustrated in <a href="#ijms-25-12570-f003" class="html-fig">Figure 3</a>.</p>
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23 pages, 4802 KiB  
Review
Stromatolites and Their “Kin” as Living Microbialites in Contemporary Settings Linked to a Long Fossil Record
by Ed Landing and Markes E. Johnson
J. Mar. Sci. Eng. 2024, 12(12), 2127; https://doi.org/10.3390/jmse12122127 - 22 Nov 2024
Viewed by 568
Abstract
Organo-sedimentary deposits that result from fine-grained sediment trapping, binding, and likely precipitation (of carbonate) by microbes in flat-mat, branching, and dome-shaped constructions are termed microbialites. They were first identified as stromatolites by paleontologists well before the discovery of cyanobacteria that build the same [...] Read more.
Organo-sedimentary deposits that result from fine-grained sediment trapping, binding, and likely precipitation (of carbonate) by microbes in flat-mat, branching, and dome-shaped constructions are termed microbialites. They were first identified as stromatolites by paleontologists well before the discovery of cyanobacteria that build the same kinds of structures in contemporary settings around the world. Earth’s earliest life forms were prokaryotes (bacteria and bacteria-like forms) that reproduced under anaerobic conditions and later produced increasingly aerobic conditions. Stromatolites persisted through later Archean and Proterozoic times through the subsequent Phanerozoic to the present. At the start of the Cambrian Period 538 million years ago, stromatolites continued alongside rapidly diversifying plant and animal phyla during the Cambrian explosion of eukaryotic life, which have complex cells with internal structures and tissue-grade organization in multicellular taxa. The type locality exhibiting clear examples of stromatolite structures is conserved at Lester Park near Saratoga Springs in northeastern New York State. Paleontologist James Hall (1811–1898) was the first in 1884 to assign a Latin binomen (Cryptozoon proliferum) to stromatolite fossils from Lester Park. Thereafter, reports on formally named stromatolites proliferated, as did examples from virtually all subsequent geological time intervals including the Pleistocene Epoch. However, recognition that living cyanobacteria formed stromatolites identified as Cryptozoon took place much later in 1961 with the announcement by geologist Brian W. Logan (1933–2008) who described modern constructions in Hamlin Pool, Shark Bay, Western Australia. Initially, Shark Bay was regarded as a one-of-a-kind sanctuary for stromatolites living under restricted conditions with elevated levels of salinity that prohibited competition or grazing by eukaryotes. Most notably, among other settings with living stromatolites discovered and described since then are the Bahamas, East African rift lakes, Mexico’s Baja California, and saline lakes in Argentina. This report reviews the history of discoveries of modern-day stromatolites, more commonly called microbialites by biologists. All are predicated on the ground-breaking efforts of geologists and paleontologists who first described fossil stromatolites but were unaware of their living counterparts. The Lester Park locality is highlighted together with a master list of other North American localities that feature purported Cryptozoons. Full article
(This article belongs to the Special Issue Feature Review Papers in Geological Oceanography)
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<p>Global representation of today’s continents and oceans on a Mollweide projection showing major ocean spreading zones. Numerals on black triangles denote the locations of oligotrophic stromatolites living today in (1) Shark Bay, Western Australia; (2) Bahamas; (3) Lake Tanganyika, Africa; (4) saline lakes in northwestern Argentina; and (5) saline ponds in Mexico’s Baja California. The numbered black dot marks the location of fossil stromatolites from present-day Upper New York State (1).</p>
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<p>Maps showing the coast of Western Australia on the Indian Ocean: (<b>a</b>) Western Australia with a small arrow pointing to Shark Bay; and (<b>b</b>) enlargement showing the location of the Hamelin Pool Marine Nature Reserve (asterisk) within the UNESCO World Heritage zone protecting the greater Shark Bay.</p>
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<p>Examples of stromatolites shaped like large bread loaves oriented perpendicular to the shore at the Hamelin Pool Marine Nature Reserve, Shark Bay: (<b>a</b>) stromatolites exposed during low tide (pocket knife 9 cm long for scale); (<b>b</b>) stromatolites barely awash at high tide with narrow, open galleries from 10 to 20 cm wide.</p>
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<p>A field of living stromatolites in permanently subtidal seawater offshore Carbla Point near Hamelin Pool in Shark Bay. Junior author for scale.</p>
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<p>Maps showing Mexico’s Isla Ángel de la Guarda in relation to the Baja California peninsula: (<b>a</b>) the full peninsula adjacent to the Gulf of California off the Mexican mainland with the island’s location (asterisk) near the head of the gulf; (<b>b</b>) map of Isla Ángel de la Guarda marking the four localities (blue) where stromatolites occur in closed lagoons; and (<b>c</b>) topographic map enlarged from box in (<b>b</b>) showing the island’s southeast end, where thrombolites and mat-forming stromatolites were discovered in 2007.</p>
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<p>Photos showing living stromatolites from closed lagoons on the shores of southeast Isla Ángel de la Guarda (see <a href="#jmse-12-02127-f005" class="html-fig">Figure 5</a>c for location): (<b>a</b>) thrombolite assemblage of branched forms the size of small cauliflower heads from the small lagoon (coin 2.4 cm in diameter for scale); (<b>b</b>) matted microbialites dissected by desiccation polygons along the shore of the big lagoon (compass case 10 cm across for scale).</p>
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<p>Location of Lester Park in the Upper Cambrian–Upper Ordovician lowlands southeast of the Mesoproterozoic Adirondack Mountains massif, northeast of the upper Middle Devonian Catskill Highlands, and west from the terminal Ediacaran–lower Upper Ordovician Taconic Allochthon.</p>
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<p>Coalesced topotype specimens of the first-named stromatolite <span class="html-italic">Cryptozoon proliferum</span> Hall, 1884, at Lester Park, Saratoga County, eastern New York: (<b>a</b>) View of the top of a shoaling cycle abraded and truncated to show growth laminae by the movement of coarse quartz sand that weathers brownish; narrower, lower parts of domes (upper part of the figure) were exposed by glacial (Pleistocene) plucking of the upper part of domes. (<b>b</b>) Detail of clotted thrombolite structure surrounded by bedded limestone from Hoyt quarry, ca. 5 m above the <span class="html-italic">C</span>. <span class="html-italic">proliferum</span> surface at Lester Park. Hammer (30 cm) for scale in both pictures.</p>
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<p><span class="html-italic">Cryptozoon proliferum</span> from older Galway Formation (lower Upper Cambrian <span class="html-italic">Elvina</span> Zone) NE of Lester Park shows two generations of fracturing: (1) brownish carbonate mud-filled cracks in the lower part of the specimen that separate and also run transverse to growth laminae are syndepositional fractures (ca. 490 Ma) and reflect continued extension of the rifted margin of NE Laurentia; (2) thin white calcite veins parallel to growth laminae produced during the Taconic orogeny (ca. 460 Ma) [<a href="#B74-jmse-12-02127" class="html-bibr">74</a>]. Hypotype NYSM 19512 from the middle of the Galway Formation railroad cut above U.S. Route 9 just N of the intersection of U.S. Route 9 with Daniels Road [<a href="#B74-jmse-12-02127" class="html-bibr">74</a>], with a USD 25 cent coin (23 mm) for scale.</p>
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<p>Small <span class="html-italic">Crytozoon proliferum</span> dome at the north end of the Lester Park surface. This specimen was termed a “microatoll” [<a href="#B26-jmse-12-02127" class="html-bibr">26</a>], but it has an erosion-truncated top and lateral margins and is surrounded by a coarse-grained sandstone with light grey-colored <span class="html-italic">C. proliferum</span> clasts (yellow arrows).</p>
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13 pages, 1775 KiB  
Article
Convergent Evolution of Armor: Thermal Resistance in Deep-Sea Hydrothermal Vent Crustaceans
by Boongho Cho, Sook-Jin Jang, Hee-seung Hwang and Taewon Kim
Biology 2024, 13(12), 956; https://doi.org/10.3390/biology13120956 - 21 Nov 2024
Viewed by 411
Abstract
Organisms occupy diverse ecological niches worldwide, each with characteristics finely evolved for their environments. Crustaceans residing in deep-sea hydrothermal vents, recognized as one of Earth’s extreme environments, may have adapted to withstand severe conditions, including elevated temperatures and pressure. This study compares the [...] Read more.
Organisms occupy diverse ecological niches worldwide, each with characteristics finely evolved for their environments. Crustaceans residing in deep-sea hydrothermal vents, recognized as one of Earth’s extreme environments, may have adapted to withstand severe conditions, including elevated temperatures and pressure. This study compares the exoskeletons of two vent crustaceans (bythograeid crab Austinograea sp. and squat lobster Munidopsis lauensis) with four coastal species (Asian paddle crabs, blue crab, hermit crab, and mantis shrimp) to identify traits influenced by vent environments. The goal was to identify distinctive exoskeletal characteristics commonly observed in vent crustaceans, resulting from their exposure to severe abiotic factors, including elevated temperatures and pressures, found in vent environments. Results show that the exoskeletons of vent crustaceans demonstrated significantly enhanced thermal stability compared to coastal species. These vent crustaceans consistently featured exoskeletons characterized by a reduced proportion of volatile components, such as water, and an increased proportion of CaCO3, compared with coastal crustaceans. Furthermore, vent crustaceans lacked carotenoid pigments that had low heat resistance. However, no apparent differences were observed in the mechanical properties. Our findings suggest that the similar composition of exoskeletons in vent crustaceans evolved convergently to withstand high temperatures. Full article
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<p>Research was conducted on species (<b>a</b>), sampling sites (<b>b</b>), and phylogenetic relationships (<b>c</b>). The phylogenetic relationship was estimated using two specimens of each species based on BI and ML analysis using the combined data set (2101 bp) of <span class="html-italic">mtCOI</span>, <span class="html-italic">mt16S rRNA</span>, <span class="html-italic">18S rRNA</span>, and <span class="html-italic">H3</span> genes. The number at each node represents the bootstrap values from ML analysis, and the posterior probabilities from BI. The scale bar indicates phylogenetic distance of 0.03 nucleotide substitutions per site.</p>
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<p>Mechanical properties and thickness ratio of each layer of the exoskeleton. (<b>a</b>) hardness, (<b>b</b>) reduced modulus, and (<b>c</b>) thickness ratio; mean ± SE; the significant difference is indicated by an asterisk (*).</p>
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<p>Crustacean exoskeleton (endocuticle layer) compound analysis graph through Raman analysis.</p>
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<p>Thermal stability analysis results. (<b>a</b>) TGA curve of crustaceans and each combusting substance on each range. Weight loss (%) for each temperature range: (<b>b</b>) Range 1, Range 2, and Range 3; mean ± SE; the significant difference is indicated by an asterisk (*).</p>
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1 pages, 161 KiB  
Correction
Correction: Alvarado et al. Alginate–Bentonite Encapsulation of Extremophillic Bacterial Consortia Enhances Chenopodium quinoa Tolerance to Metal Stress. Microorganisms 2024, 12, 2066
by Roxana Alvarado, Cesar Arriagada-Escamilla, Javier Ortiz, Reinaldo Campos-Vargas and Pablo Cornejo
Microorganisms 2024, 12(11), 2356; https://doi.org/10.3390/microorganisms12112356 - 19 Nov 2024
Viewed by 231
Abstract
In the original publication [...] Full article
(This article belongs to the Special Issue Rhizosphere Bacteria and Fungi That Promote Plant Growth)
14 pages, 603 KiB  
Review
Extremophiles and Extremophilic Behaviour—New Insights and Perspectives
by George N. Angelakis, Chrysianna Psarologaki, Stergios Pirintsos and Kiriakos Kotzabasis
Life 2024, 14(11), 1425; https://doi.org/10.3390/life14111425 - 5 Nov 2024
Viewed by 1078
Abstract
Extremophiles, throughout evolutionary time, have evolved a plethora of unique strategies to overcome hardships associated with the environments they are found in. Modifying their genome, showing a bias towards certain amino acids, redesigning their proteins, and enhancing their membranes and other organelles with [...] Read more.
Extremophiles, throughout evolutionary time, have evolved a plethora of unique strategies to overcome hardships associated with the environments they are found in. Modifying their genome, showing a bias towards certain amino acids, redesigning their proteins, and enhancing their membranes and other organelles with specialised chemical compounds are only some of those strategies. Scientists can utilise such attributes of theirs for a plethora of biotechnological and astrobiological applications. Moreover, the rigorous study of such microorganisms regarding their evolution and ecological niche can offer deep insight into science’s most paramount inquiries such as how life originated on Earth and whether we are alone in the universe. The intensification of studies involving extremophiles in the future can prove to be highly beneficial for humanity, even potentially ameliorating modern problems such as those related to climate change while also expanding our knowledge about the complex biochemical reactions that ultimately resulted in life as we know it today. Full article
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<p>A simplified scheme that presents the differences between extremophiles and extremotolerant organisms while integrating niche theories and new concepts like S-space.</p>
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14 pages, 3820 KiB  
Article
Microbial Mat Dominated by Amphora spp. and Their Adaptative Strategies in an Arsenic-Rich Brackish Pond
by Eleonora Agostino, Angela Macrì, Vincenzo Zammuto, Michela D’Alessandro, Marco Sebastiano Nicolò, Salvatore Giacobbe and Concetta Gugliandolo
J. Mar. Sci. Eng. 2024, 12(11), 1966; https://doi.org/10.3390/jmse12111966 - 1 Nov 2024
Viewed by 477
Abstract
Marine diatoms are essential members of both phytoplankton and phytobenthic communities, able to colonize submerged artificial and natural surfaces, contributing to benthic microbial biomass. Diatoms have developed different adaptative mechanisms to cope with various environmental stresses, including high concentrations of heavy metals. The [...] Read more.
Marine diatoms are essential members of both phytoplankton and phytobenthic communities, able to colonize submerged artificial and natural surfaces, contributing to benthic microbial biomass. Diatoms have developed different adaptative mechanisms to cope with various environmental stresses, including high concentrations of heavy metals. The aim of this study was to investigate the arsenic resistance of diatoms, isolated from microbial mats collected from an arsenic-rich brackish pond (Lake Mergolo della Tonnara, Italy), by evaluating (i) their ability to form biofilms in the presence of arsenite (AsIII) or arsenate (AsV), and (ii) the variations in the photosynthetic pigments’ contents (i.e., chlorophyll a and c) in their biofilms. The mats were dominated by members of the genus Amphora, and isolates were affiliated with species of A. capitellata, A. coffeaeformis, and A. montana. The strains grew better in the presence of AsV than AsIII, which is generally less toxic. After seven days of incubation, each strain exhibited a different ability to form biofilms on glass surfaces in the presence of arsenic (25 ppm), with A. montana strain 27 being the most effective (86%) in the presence of AsIII, and A. coffeaeformis strain 26 (74%) with AsV. Photosynthetic pigment levels (chlorophyll a and c) differed in each biofilm, being poorly reduced by AsIII in strain 27, and by AsV in strain 26, indicating a species-specific response to arsenic stress. Our results indicated that Amphora species thriving in this environment can form biofilms as an As-resistance mechanism, maintain their levels of photosynthetic pigments, and support the functioning of the pond ecosystem, with A. montana being favored in the presence of AsIII, whereas A. coffeaeformis 26 in the presence of AsV. As producers of biofilms, these strains could be useful to develop new strategies to remediate arsenic pollution. Full article
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<p>The study area of the Oliveri-Tindari Lagoon (Gulf of Patti, Sicily, Italy) including Lake Verde, Lake Fondo Porto and Lake Mergolo della Tonnara.</p>
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<p>Micrograph of isolated diatoms: (<b>a</b>) strain 24, (<b>b</b>) strain 26, and (<b>c</b>) strain 27 (60×).</p>
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<p>Growth curves of <span class="html-italic">A. capitellata</span> 24, <span class="html-italic">A. coffeaeformis</span> 26, and <span class="html-italic">A. montana</span> 27 in f/2 medium under different concentrations, i.e., 0 (control), 12.5, 17, 25, and 34 ppm of As<sup>III</sup> or As<sup>V</sup>. The graphs show data from triplicate experiments (mean ± SD).</p>
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<p>As<sup>III</sup> (a) or As<sup>V</sup> (b) (from 12.5 to 34 ppm) toxicity, expressed as EC<sub>50</sub>, on the viability of <span class="html-italic">A. capitellata</span> 24, <span class="html-italic">A. coffeaeformis</span> 26, and <span class="html-italic">A. montana</span> 27. The bars represent mean ± SD for three replicates (n = 3). Statistical differences were evaluated using two-way ANOVA with Tukey’s multiple comparisons tests. Different lowercase letters above the bar graph indicate significant statistical differences (<span class="html-italic">p</span> ≤ 0.05).</p>
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<p>Adhesion of (<b>a</b>) <span class="html-italic">A. capitellata</span> 24, (<b>b</b>) <span class="html-italic">A. coffeaeformis</span> 26, and (<b>c</b>) <span class="html-italic">A. montana</span> 27 onto glass surfaces after four days of incubation in the absence or presence of As<sup>III</sup> or As<sup>V</sup> (25 ppm).</p>
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<p>Biofilm formation (%) by <span class="html-italic">A. capitellata</span> 24 (<b>a</b>), <span class="html-italic">A. coffeaeformis</span> 26 (<b>b</b>), and <span class="html-italic">A. montana</span> 27 (<b>c</b>) on glass surfaces in the absence (control) or in the presence of As<sup>III</sup> or As<sup>V</sup> (25 ppm) at different times. Statistical differences were evaluated using a two-way ANOVA. * <span class="html-italic">p</span> ≤ 0.05 and ** <span class="html-italic">p</span> ≤ 0.01, significant statistical differences compared to the control.</p>
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<p>Three-dimensional models of biofilms of the most resistant strains: (<b>a</b>) <span class="html-italic">A. montana</span> 27 in the absence (control) or presence of As<sup>III</sup> and (<b>b</b>) <span class="html-italic">A. coffeaeformis</span> 26 in the absence (control) or presence of As<sup>V</sup>.</p>
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<p>Chlorophyll <span class="html-italic">a</span> and chlorophyll <span class="html-italic">c</span> content (%) in <span class="html-italic">A. capitellata</span> 24, <span class="html-italic">A. coffeaeformis</span> 26, and <span class="html-italic">A. montana</span> 27 biofilms in the presence or absence of As<sup>III</sup> (<b>a</b>) or As<sup>V</sup> (<b>b</b>), quantified by spectrophotometric analysis. Statistical differences were evaluated using a two-way ANOVA. ** <span class="html-italic">p</span> ≤ 0.01, significant statistical differences compared to the control.</p>
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<p>Chlorophyll <span class="html-italic">a</span> and chlorophyll <span class="html-italic">c</span> concentrations (µg mL<sup>−1</sup>) in <span class="html-italic">A. capitellata</span> 24, <span class="html-italic">A. coffeaeformis</span> 26, and <span class="html-italic">A. montana</span> 27 biofilms in the presence or absence of As<sup>III</sup> (<b>a</b>) or As<sup>V</sup> (<b>b</b>), quantified by spectrophotometric analysis.</p>
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16 pages, 1967 KiB  
Article
Cold-Active Lipase from the Ice Cave Psychrobacter SC65A.3 Strain, a Promising Biocatalyst for Silybin Acylation
by Victoria I. Paun, Sabina G. Ion, Giulia R. Gheorghita, Iunia Podolean, Madalina Tudorache and Cristina Purcarea
Molecules 2024, 29(21), 5125; https://doi.org/10.3390/molecules29215125 - 30 Oct 2024
Viewed by 487
Abstract
Cold-active lipase from the psychrophilic bacterial strain Psychrobacter SC65A.3 isolated from Scarisoara Ice Cave (Romania) was cloned and characterized as an extremophilic biocatalyst for silybin acylation. Structural analyses highlighted conserved motifs confirming a functional lipase and the presence of primary structure elements for [...] Read more.
Cold-active lipase from the psychrophilic bacterial strain Psychrobacter SC65A.3 isolated from Scarisoara Ice Cave (Romania) was cloned and characterized as an extremophilic biocatalyst for silybin acylation. Structural analyses highlighted conserved motifs confirming a functional lipase and the presence of primary structure elements for catalysis at low temperatures. The recombinant enzyme (PSL2) heterologously expressed in Escherichia coli was purified in one step by affinity chromatography with a yield of 12.08 ± 1.72 µg L−1 of culture and a specific activity of 20.1 ± 3.2 U mg−1 at 25 °C. Functional characterization of PSL2 showed a neutral (7.2) optimal pH and a high thermal stability up to 90 °C. Also, this lipase was stable in the presence of different organic solvents, with 60% residual activity when using 20% DMSO. Kinetic measurements indicated performant catalytic efficiency of PSL2 for different short and long chain fatty acids, with Km in the mM range. The catalytic activity of PSL2 was assessed for silybin acylation with various fatty acids and fatty acid methyl esters, demonstrating a 90% silybin conversion when methyl decanoate ester was used. This result clearly highlights the biocatalytic capability of this new cold-active lipase. Full article
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<p>Multiple alignment of the primary PSL2 sequence with homologous enzymes from the psychrophilic <span class="html-italic">Psychrobacter</span> sp. G [WP 020444543] (PG) and <span class="html-italic">Moritella</span> sp. PE36 [WP 198138589] (MO), the mesophilic <span class="html-italic">Bacillus subtilis</span> [WP 161476533] (BS) and <span class="html-italic">Pseudomonas aeruginosa</span> [EIU5571796] (PA), and the hyperthermophilic <span class="html-italic">Sulfolobus islandicus</span> [WP 015580697] (SI). Identical (stars) and conserved (dots) residues from all enzymes, active site residues (bold), catalytic His444 (red), and conserved motifs (boxes) are shown. Amino acid numbers for each enzyme primary structure are indicated.</p>
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<p>pH effect on the PSL2 activity. The lipase activity was measured at 25 °C in the presence of 2.5 mM <span class="html-italic">p</span>-NPB and 50 mM PBS (pH 6.0–7.0) or 50 mM Tris HCl buffer (pH 7.0–9.0) using 51 µg of PSL2, as indicated in the Methods. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>Solvent tolerance stability of PSL2. The lipase activity was measured at 25 °C using 40.8 µg of PSL2 and 3.75 mM <span class="html-italic">p</span>-NPB as the substrate in the presence of ethanol (EtOH), dimethyl sulfoxide (DMSO), dimethylformamide (DMF), and tetrahydrofuran (THF) at final concentrations ranging from 0% to 20% (<span class="html-italic">v/v</span>). The relative activity in the absence of solvent was calculated as 100%. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>Substrate specificity of PSL2. The specific activity was measured at 25 °C (yellow) and 40 °C (green), as indicated in the Methods, using <span class="html-italic">p</span>-nitrophenyl stearate (<span class="html-italic">p</span>-NPS), <span class="html-italic">p</span>-nitrophenyl palmitate (<span class="html-italic">p</span>-NPP), and <span class="html-italic">p</span>-nitrophenyl butyrate (<span class="html-italic">p</span>-NPB) as the substrates and 16.8 µg of PSL2. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>Thermal stability of PSL2. The enzyme (4 µg) was incubated at various temperatures in the 4 °C–90 °C interval for 30 min and the activity was measured at 25 °C using <span class="html-italic">p</span>-NPP as the substrate (see the Methods). The relative activity in the absence of thermal treatment was calculated as 100%. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>Influence of the acylation reagents on the silybin derivatization. Experimental conditions: 2 mM silybin, acylation reagent, and 0.31% PSL2 lipase (<span class="html-italic">v</span>/<span class="html-italic">v</span>) in THF; 1000 rpm, 24 h, 25 °C. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>The effect of the PSL2 concentration on the silybin acylation. Experimental conditions: 2 mM silybin, 45 mM Me-decanoate, and PSL2 lipase in THF; 1000 rpm, 24 h, 25 °C. Average and standard deviation values of specific activities were calculated based on triplicate measurements.</p>
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<p>Variation of the reaction time for silybin acylation. Experimental conditions: 2 mM silybin in THF, 45 mM Me-decanoate, and 0.31% PSL2 lipase (<span class="html-italic">v/v</span>), 1000 rpm, 25 °C.</p>
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21 pages, 1995 KiB  
Article
Alginate–Bentonite Encapsulation of Extremophillic Bacterial Consortia Enhances Chenopodium quinoa Tolerance to Metal Stress
by Roxana Alvarado, Cesar Arriagada-Escamilla, Javier Ortiz, Reinaldo Campos-Vargas and Pablo Cornejo
Microorganisms 2024, 12(10), 2066; https://doi.org/10.3390/microorganisms12102066 - 15 Oct 2024
Viewed by 944 | Correction
Abstract
This study explores the encapsulation in alginate/bentonite beads of two metal(loid)-resistant bacterial consortia (consortium A: Pseudomonas sp. and Bacillus sp.; consortium B: Pseudomonas sp. and Bacillus sp.) from the Atacama Desert (northern Chile) and Antarctica, and their influence on physiological traits of Chenopodium [...] Read more.
This study explores the encapsulation in alginate/bentonite beads of two metal(loid)-resistant bacterial consortia (consortium A: Pseudomonas sp. and Bacillus sp.; consortium B: Pseudomonas sp. and Bacillus sp.) from the Atacama Desert (northern Chile) and Antarctica, and their influence on physiological traits of Chenopodium quinoa growing in metal(loid)-contaminated soils. The metal(loid) sorption capacity of the consortia was determined. Bacteria were encapsulated using ionic gelation and were inoculated in soil of C. quinoa. The morphological variables, photosynthetic pigments, and lipid peroxidation in plants were evaluated. Consortium A showed a significantly higher biosorption capacity than consortium B, especially for As and Cu. The highest viability of consortia was achieved with matrices A1 (3% alginate and 2% bentonite) and A3 (3% alginate, 2% bentonite and 2.5% LB medium) at a drying temperature of 25 °C and storage at 4 °C. After 12 months, the highest viability was detected using matrix A1 with a concentration of 106 CFU g−1. Further, a greenhouse experiment using these consortia in C. quinoa plants showed that, 90 days after inoculation, the morphological traits of both consortia improved. Chemical analysis of metal(loid) contents in the leaves indicated that consortium B reduced the absorption of Cu to 32.1 mg kg−1 and that of Mn to 171.9 mg kg−1. Encapsulation resulted in a significant increase in bacterial survival. This highlights the benefits of using encapsulated microbial consortia from extreme environments, stimulating the growth of C. quinoa, especially in soils with metal(loid) levels that can be a serious constraint for plant growth. Full article
(This article belongs to the Special Issue Rhizosphere Bacteria and Fungi That Promote Plant Growth)
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<p>(<b>A</b>): Biosorption and (<b>B</b>): removal efficiency of the metal(loid)s by consortium A and consortium B. CI: metal(loid) mix I. CII: metal(loid) mix II. AI: metal(loid) mix I with consortium A. AII: metals(loid) mix II with consortium A. BI: metal(loid) mix I with consortium B. BII: metals(loid) mix II with consortium B. Different letters above bars indicate significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05, n = 6).</p>
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<p>Survival of bacterial consortia A and B in different matrices. Matrix (A1 alginate 3% bentonite 2%), matrix A2 (alginate 3% bentonite 2% glycerol 3%), matrix A3 (alginate 3%, bentonite 2%, LB medium 2.5%), and matrix A4 (alginate 3% molasses 3%). The beads were dried at 25, 28, 30, and 35 °C for 24 h. N<sub>t</sub> is the number of viable cells after drying, N<sub>i</sub> is the number of viable cells at time zero. The initial cell count was approximately 10<sup>9</sup> CFU g<sup>−1</sup>. The different letters indicate a statistically significant difference between the groups <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Viability of bacterial consortia A and B after 12 months of storage at 4 and 24 °C using different encapsulation matrices. Matrix A1 (3% alginate and 2% bentonite) and matrix A3 (3% alginate, 2% bentonite, and 2.5% LB medium). The initial cell count was approximately 10<sup>8</sup> CFU g<sup>−1</sup>. Error bars indicate the standard deviation of 6 independent replicates. Lowercase letters indicate a significant difference between temperatures for each treatment and uppercase letters indicate a significant difference between matrices; <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Spearman’s rank correlation analysis between consortium, matrix, metal(loid) mix, and morphological traits of <span class="html-italic">C. quinoa</span>. The cells are colored according to the correlation coefficient. Blue represents a significant positive correlation and red represents a significant negative correlation.</p>
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<p>Total chlorophyll content in <span class="html-italic">C. quinoa</span> plants WC: without consortium, CA: with consortium A, and CB: with consortium B; matrix A1 (3% alginate and 2% bentonite) and matrix A3 (3% alginate, 2% bentonite, and 2.5% LB medium) in different concentrations of metal(loid)s. (<b>a</b>) Control: soil without the metal(loid) mix; (<b>b</b>) metal(loid) mix I, and (<b>c</b>) metal(loid) mix II. Error bars indicate the standard deviation of 6 independent replicates. Lower-case letters indicate a significant difference between matrices for each treatment and upper-case letters indicate a significant difference between treatments <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Malondialdehyde (MDA) content in leaves and roots of <span class="html-italic">C. quinoa</span> plants. WC: without consortium, CA: with consortium A and CB: with consortium B; Matrix A1 (3% alginate and 2% bentonite) and matrix A3 (3% alginate, 2% bentonite, and 2.5% LB medium) in different concentrations of metal(loid)s. (<b>a</b>,<b>d</b>) Control: soil without the metal(loid) mix; (<b>b</b>,<b>e</b>) metal(loid) mix I and (<b>c</b>,<b>f</b>) metal(loid) mix II. Error bars indicate the standard deviation of 6 independent replicates. Lower-case letters indicate a significant difference between matrices for each treatment and upper-case letters indicate a significant difference between treatments <span class="html-italic">p</span> &lt; 0.05.</p>
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19 pages, 7674 KiB  
Article
Microbial Community Structure in the Taklimakan Desert: The Importance of Nutrient Levels in Medium and Culture Methods
by Feng Wen, Siyuan Wu, Xiaoxia Luo, Linquan Bai and Zhanfeng Xia
Biology 2024, 13(10), 797; https://doi.org/10.3390/biology13100797 - 6 Oct 2024
Viewed by 746
Abstract
Although the Taklimakan Desert lacks the necessary nutrients and conditions to support an extensive ecosystem, it is a treasure trove of extremophile resources with special structures and functions. We analyzed the bacterial communities using oligotrophic medium and velvet cloth replicate combined with an [...] Read more.
Although the Taklimakan Desert lacks the necessary nutrients and conditions to support an extensive ecosystem, it is a treasure trove of extremophile resources with special structures and functions. We analyzed the bacterial communities using oligotrophic medium and velvet cloth replicate combined with an extended culture duration. We isolated numerous uncultured microorganisms and rare microorganisms belonging to genera not often isolated or recently described, such as Aliihoeflea, Halodurantibacterium, and Indioceanicola. A total of 669 strains were isolated from the soil of the Taklimakan Desert, which were classified into 5 phyla, 7 classes, 25 orders, 42 families, 83 genera, and 379 species. Among them, 148 strains were potential new species. Our data show that even when working with samples from extreme environments, simple approaches are still useful for cultivating stubborn microbes. Through comparing the isolation effects of different nutrient levels on microbial diversity and abundance, the results show that reducing the nutrient level of the medium was more conducive to improving the culturability of microorganisms in low-nutrient environments, while the high-nutrient medium was more suitable for the isolation of dominant fast-growing strains. This study helps to better reflect the diversity of microbial resources and lays a foundation for the further research and utilization of soil microbial resources in the Taklimakan Desert. Full article
(This article belongs to the Section Conservation Biology and Biodiversity)
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<p>Sample collection points in Taklimakan Desert. Note: A: South, B: North, C: West, D: East, E: Central.</p>
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<p>PCoA analysis of five sand samples in the Taklimakan Desert. Note: A: South, B: North, C: West, D: East, E: Central.</p>
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<p>The top ten categories of bacteria at different taxonomic levels: (<b>a</b>) phylum, (<b>b</b>) class, (<b>c</b>) order, (<b>d</b>) family, and (<b>e</b>) genus. Note: A: South, B: North, C: West, D: East, E: Central.</p>
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<p>Total number of soil microbial plate colonies isolated on media of different nutrient levels. Note: A: South, B: North, C: West, D: East, E: Central.</p>
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<p>Microorganisms isolated from five soil samples from the Taklimakan Desert. The chord plot (<b>a</b>) of the bacterial community in the desert samples represents the difference in the distribution of microorganisms obtained from the five Taklimakan Desert soil samples. The Venn diagram of the bacterial community in the desert sample represents the quantitative distribution of genus (<b>b</b>). These samples are represented by different circles: a Venn diagram representing the number of genera detected in each sample and the overlap of genera in the sample.</p>
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<p>Microorganisms isolated from five soil samples from the Taklimakan Desert. The chord plot (<b>a</b>) of the bacterial community in the desert samples represents the difference in the distribution of microorganisms obtained from the five Taklimakan Desert soil samples. The Venn diagram of the bacterial community in the desert sample represents the quantitative distribution of genus (<b>b</b>). These samples are represented by different circles: a Venn diagram representing the number of genera detected in each sample and the overlap of genera in the sample.</p>
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<p>Microorganisms isolated from the Taklimakan Desert at different medium nutrient levels.</p>
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<p>Proportion of rare bacteria in each nutrient level medium.</p>
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27 pages, 2689 KiB  
Review
Novel Approach of Tackling Wax Deposition Problems in Pipeline Using Enzymatic Degradation Process: Challenges and Potential Solutions
by Shazleen Saadon, Raja Noor Zaliha Raja Abd Rahman, Nor Hafizah Ahmad Kamarudin, Sara Shahruddin, Siti Rohaida Mohd Shafian, Norhidayah Ahmad Wazir and Mohd Shukuri Mohamad Ali
Processes 2024, 12(10), 2074; https://doi.org/10.3390/pr12102074 - 25 Sep 2024
Viewed by 890
Abstract
Anthropogenic activities have led to hydrocarbon spills, and while traditional bioremediation methods are costly and time-consuming, recent research has focused on engineered enzymes for managing pollutant. The potential of enzymes for resolving wax flow problems in the petroleum industry remains unexplored. This paper [...] Read more.
Anthropogenic activities have led to hydrocarbon spills, and while traditional bioremediation methods are costly and time-consuming, recent research has focused on engineered enzymes for managing pollutant. The potential of enzymes for resolving wax flow problems in the petroleum industry remains unexplored. This paper offers a comprehensive review of the current state of research activities related to the bioremediation of petroleum-polluted sites and the biodegradation of specific petroleum hydrocarbons. The assayed enzymes that took part in the degradation were discussed in detail. Lipase, laccase, alkane hydroxylase, alcohol dehydrogenase, esterase, AlkB homologs and cytochrome P450 monooxygenase are among the enzymes responsible for the degradation of more than 50% of the hydrocarbons in contaminated soil and wastewater and found to be active on carbon C8 to C40. The possible biodegradation mechanism of petroleum hydrocarbons was also elucidated. The enzymes’ primary metabolic pathways include terminal, subterminal, and ω-oxidation. Next, given the successful evidence of the hydrocarbon treatment efficiency, the authors analyzed the opportunity for the enzymatic degradation approach if it were to be applied to a different scenario: managing wax deposition in petroleum-production lines. With properties such as high transformation efficiency and high specificity, enzymes can be utilized for the treatment of viscous heavy oil for transportability, evidenced by the 20 to 99% removal of hydrocarbons. The challenges associated with the new approach are also discussed. The production cost of enzymes, the characteristics of hydrocarbons and the operating conditions of the production line may affect the biocatalysis reaction to some extent. However, the challenges can be overcome by the usage of extremophilic enzymes. The combination of technological advancement and deployment strategies such as the immobilization of a consortium of highly thermophilic and halotolerant enzymes is suggested. Recovering and reusing enzymes offers an excellent strategy to improve the economics of the technology. This paper provides insights into the opportunity for the enzymatic degradation approach to be expanded for wax deposition problems in pipelines. Full article
(This article belongs to the Special Issue Application of Enzymes in Sustainable Biocatalysis)
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<p>Locations of significant historical oil-spill incidents [<a href="#B6-processes-12-02074" class="html-bibr">6</a>].</p>
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<p>Exploiting biocatalytic degradation of hydrocarbon technique for new purpose.</p>
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<p>Research publications on “biocatalytic degradation”, “pollutants” and “wax”, based on data obtained from Google Scholar on 3 August 2024.</p>
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<p>Reported alkane-degrading pathways, adopted and re-illustrated from Beilen et al., 2007 [<a href="#B79-processes-12-02074" class="html-bibr">79</a>].</p>
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<p>Illustration on using enzyme consortium consisting of different types of biocatalyst for paraffin wax degradation.</p>
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<p>Illustration of how the amorphous region of petroleum is more susceptible to enzyme attack than the crystalline region (re-illustrated from Wei and Zimmerman, 2017 [<a href="#B140-processes-12-02074" class="html-bibr">140</a>]).</p>
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<p>Proposed fluidized bed reactor concept for recovery and reuse of enzyme.</p>
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16 pages, 541 KiB  
Review
Advances in Extremophile Research: Biotechnological Applications through Isolation and Identification Techniques
by Giovanni Gallo and Martina Aulitto
Life 2024, 14(9), 1205; https://doi.org/10.3390/life14091205 - 23 Sep 2024
Viewed by 3098
Abstract
Extremophiles, organisms thriving in extreme environments such as hot springs, deep-sea hydrothermal vents, and hypersaline ecosystems, have garnered significant attention due to their remarkable adaptability and biotechnological potential. This review presents recent advancements in isolating and characterizing extremophiles, highlighting their applications in enzyme [...] Read more.
Extremophiles, organisms thriving in extreme environments such as hot springs, deep-sea hydrothermal vents, and hypersaline ecosystems, have garnered significant attention due to their remarkable adaptability and biotechnological potential. This review presents recent advancements in isolating and characterizing extremophiles, highlighting their applications in enzyme production, bioplastics, environmental management, and space exploration. The unique biological mechanisms of extremophiles offer valuable insights into life’s resilience and potential uses in industry and astrobiology. Full article
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<p>Schematic overview of the main environments where extremophilic microorganisms are found.</p>
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46 pages, 3736 KiB  
Review
Exploring Extremotolerant and Extremophilic Microalgae: New Frontiers in Sustainable Biotechnological Applications
by Dorian Rojas-Villalta, David Rojas-Rodríguez, Melany Villanueva-Ilama, Rossy Guillén-Watson, Francinie Murillo-Vega, Olman Gómez-Espinoza and Kattia Núñez-Montero
Biology 2024, 13(9), 712; https://doi.org/10.3390/biology13090712 - 11 Sep 2024
Viewed by 2453
Abstract
Exploring extremotolerant and extremophilic microalgae opens new frontiers in sustainable biotechnological applications. These microorganisms thrive in extreme environments and exhibit specialized metabolic pathways, making them valuable for various industries. The study focuses on the ecological adaptation and biotechnological potential of these microalgae, highlighting [...] Read more.
Exploring extremotolerant and extremophilic microalgae opens new frontiers in sustainable biotechnological applications. These microorganisms thrive in extreme environments and exhibit specialized metabolic pathways, making them valuable for various industries. The study focuses on the ecological adaptation and biotechnological potential of these microalgae, highlighting their ability to produce bioactive compounds under stress conditions. The literature reveals that extremophilic microalgae can significantly enhance biomass production, reduce contamination risks in large-scale systems, and produce valuable biomolecules such as carotenoids, lipids, and proteins. These insights suggest that extremophilic microalgae have promising applications in food, pharmaceutical, cosmetic, and biofuel industries, offering sustainable and efficient alternatives to traditional resources. The review concludes that further exploration and utilization of these unique microorganisms can lead to innovative and environmentally friendly solutions in biotechnology. Full article
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<p>Biochemical composition of the most-studied extremotolerant and extremophilic microalgal genera based on literature data. Superscript numbers correspond to specific references cited in this document as follows: 1—Ref. [<a href="#B10-biology-13-00712" class="html-bibr">10</a>], 2—Ref. [<a href="#B11-biology-13-00712" class="html-bibr">11</a>], 3—Ref. [<a href="#B20-biology-13-00712" class="html-bibr">20</a>], 4—Ref. [<a href="#B17-biology-13-00712" class="html-bibr">17</a>], 5—Ref. [<a href="#B14-biology-13-00712" class="html-bibr">14</a>], 6—Ref. [<a href="#B15-biology-13-00712" class="html-bibr">15</a>], 7—Ref. [<a href="#B17-biology-13-00712" class="html-bibr">17</a>], 8—Ref. [<a href="#B12-biology-13-00712" class="html-bibr">12</a>], 9—Ref. [<a href="#B13-biology-13-00712" class="html-bibr">13</a>], 10—Ref. [<a href="#B8-biology-13-00712" class="html-bibr">8</a>], 11—Ref. [<a href="#B9-biology-13-00712" class="html-bibr">9</a>].</p>
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<p>Biotechnological applications of extremophilic microalgae in the food industry. Venn diagram circles represent a summarized classification of the potential uses. Smaller circles represent examples of molecules related to corresponding application. Strains of species are ignored for simplification, please refer to <a href="#biology-13-00712-t001" class="html-table">Table 1</a> for respective strains and reference. Created with BioRender.com.</p>
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<p>Biotechnological applications of extremophilic microalgae in the textiles and cosmetic industries. Venn diagram circles represent a summarized classification of the relevant produced molecules. Smaller circles represent examples of the application related to corresponding molecules. Strains of species are ignored for simplification, please refer to <a href="#biology-13-00712-t001" class="html-table">Table 1</a> for respective strains and reference. Created with BioRender.com.</p>
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<p>Biotechnological applications of extremophilic microalgae in bioremediation and as bioindications. Venn diagram circles represent a summarized classification of the bioremediation type. Smaller circles represent examples of pollutant molecules. Strains of species are ignored for simplification, please refer to <a href="#biology-13-00712-t001" class="html-table">Table 1</a> for respective strains and reference. Created with BioRender.com.</p>
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<p>Biotechnological applications of extremophilic microalgae in the textiles and cosmetic industries. Venn diagram circles represent a summarized classification biofuel type. Smaller circles represent examples of the feedstock used for production. Strains of species are ignored for simplification, please refer to <a href="#biology-13-00712-t001" class="html-table">Table 1</a> for respective strains and reference. Created with BioRender.com.</p>
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<p>Biotechnological applications of extremophilic microalgae in the pharmaceutical industry. Venn diagram circles represent a summarized application. Smaller circles represent examples of molecules responsible for bioactive potential. Strains of species are ignored for simplification, please refer to <a href="#biology-13-00712-t001" class="html-table">Table 1</a> for respective strains and reference. Created with BioRender.com.</p>
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23 pages, 2102 KiB  
Review
Unraveling the Potentials of Extremophiles in Bioextraction of Valuable Metals from Industrial Solid Wastes: An Overview
by Adegoke Isiaka Adetunji and Mariana Erasmus
Minerals 2024, 14(9), 861; https://doi.org/10.3390/min14090861 - 24 Aug 2024
Viewed by 1119
Abstract
The continuous dumping of industrial solid wastes into the immediate environment is incommodious since these waste materials cause pollution and serious hazards to human health. In addition, these solid wastes are complex and consist of toxic chemical substances, heavy metals, and valuable metals, [...] Read more.
The continuous dumping of industrial solid wastes into the immediate environment is incommodious since these waste materials cause pollution and serious hazards to human health. In addition, these solid wastes are complex and consist of toxic chemical substances, heavy metals, and valuable metals, hence warranting treatment before disposal. Bioleaching is a green and sustainable technology for the solubilization and mobilization of metals from solid matrices. The leaching efficacy is contingent on the types and physiology of the organisms, the elemental content of the solid wastes, and the presence of appropriate bioprocess parameters at optimum conditions. Extremophilic microbes, including thermophiles, acidophiles, alkaliphiles, and halophiles, are recognized as excellent biological agents for the efficient bioextraction of metals from industrial solid wastes due to their aptitude for survival under harsh bioleaching conditions. Therefore, this review provides insights into the employability of extremophilic microorganisms as a biofactory for the recovery of valuable metals from various industrial solid wastes. More so, it discusses the sustainability of the bioleaching technique in terms of its life cycle assessment (LCA) and techno-economic analysis. Full article
(This article belongs to the Special Issue Bioleaching of Metals from Waste/Wastewater)
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<p>Schematic diagrams elucidating different industrial solid wastes.</p>
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<p>Schematic diagrams illustrating some environmental and health effects of industrial solid wastes.</p>
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<p>Schematic diagrams showing various types of extremophiles.</p>
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<p>Schematic diagrams depicting stepwise procedures for bioleaching of metals from industrial solid waste.</p>
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19 pages, 4180 KiB  
Article
Genomic Functional Analysis of Novel Radiation-Resistant Species of Knollia sp. nov. S7-12T from the North Slope of Mount Everest
by Xinyue Wang, Yang Liu, Zhiyuan Chen, Kexin Wang, Guangxiu Liu, Tuo Chen and Binglin Zhang
Microorganisms 2024, 12(9), 1748; https://doi.org/10.3390/microorganisms12091748 - 23 Aug 2024
Viewed by 877
Abstract
Radiation protection is an important field of study, as it relates to human health and environmental safety. Radiation-resistance mechanisms in extremophiles are a research hotspot, as this knowledge has great application value in bioremediation and development of anti-radiation drugs. Mount Everest, an extreme [...] Read more.
Radiation protection is an important field of study, as it relates to human health and environmental safety. Radiation-resistance mechanisms in extremophiles are a research hotspot, as this knowledge has great application value in bioremediation and development of anti-radiation drugs. Mount Everest, an extreme environment of high radiation exposure, harbors many bacterial strains resistant to radiation. However, owing to the difficulties in studying them because of the extreme terrain, many remain unexplored. In this study, a novel species (herein, S7-12T) was isolated from the moraine of Mount Everest, and its morphology and functional and genomic characteristics were analyzed. The strain S7-12T is white in color, smooth and rounded, non-spore-forming, and non-motile and can survive at a UV intensity of 1000 J/m2, showing that it is twice as resistant to radiation as Deinococcus radiodurans. Radiation-resistance genes, including IbpA and those from the rec and CspA gene families, were identified. The polyphasic taxonomic approach revealed that the strain S7-12T (=KCTC 59114T =GDMCC 1.3458T) is a new species of the genus Knoellia and is thus proposed to be named glaciei. The in-depth study of the genome of strain S7-12T will enable us to gain further insights into its potential use in radiation resistance. Understanding how microorganisms resist radiation damage could reveal potential biomarkers and therapeutic targets, leading to the discovery of potent anti-radiation compounds, thereby improving human resistance to the threat of radiation. Full article
(This article belongs to the Section Microbiomes)
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<p>Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences of the strain S7-12<sup>T</sup> and the type strains of other closely related species in the genus <span class="html-italic">Knoellia</span> and <span class="html-italic">Marihabitans</span>. <span class="html-italic">Marihabitans asiaticum</span> HG667<sup>T</sup> (AB286025) was used as an outgroup. Bar, 0.005 substitutions per nucleotide position.</p>
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<p>UBCG phylogenetic tree based on the up-to-date core gene set and pipeline of strain S7-12<sup>T</sup> and the type strains of other closely related species in the genus <span class="html-italic">Knoellia</span> and <span class="html-italic">Marihabitans</span>. <span class="html-italic">Marihabitans asiaticum</span> HG667<sup>T</sup> (AB286025) was used as an outgroup.</p>
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<p>Scanning electron microscope photos of the cells of strain S7-12<sup>T</sup>.</p>
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<p>Comparison of UV irradiation resistance and days to recovery of growth between strain S7-12<sup>T</sup> (<b>A</b>) and strain <span class="html-italic">D. radiodurans</span> (<b>B</b>).</p>
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<p>Genome comparisons of strain S7-12<sup>T</sup> and its related reference strains including the dDDH value (<b>A</b>), OrthoANI value (<b>B</b>), and AAI value (<b>C</b>). Furthermore, a–g represent S7-12<sup>T</sup>, <span class="html-italic">K. flava</span> TL1<sup>T</sup>, <span class="html-italic">K. subterranea</span> KCTC 19937<sup>T</sup>, <span class="html-italic">K. sinensis</span> KCTC 19936<sup>T</sup>, <span class="html-italic">K. remsis</span> ATCC BAA-1496<sup>T</sup>, <span class="html-italic">K. locipacati</span> DMZ1<sup>T</sup>, <span class="html-italic">K. aerolata</span> DSM 18566<sup>T</sup>, respectively.</p>
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<p>Distribution of CDS in 24 COG functional categories in strain S7-12<sup>T</sup>.</p>
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<p>Comparisons of orthologous protein groups in S7-12<sup>T</sup> and six related <span class="html-italic">Knoellia genomes</span>. (<b>A</b>) Percentage of core, dispensable, and unique genes in each of all eight genomes. (<b>B</b>) Venn diagram displaying the number of core and unique genes for each of the S7-12<sup>T</sup> and related type strains.</p>
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<p>Classification of COG functions annotated to different pan-genomes in the genus <span class="html-italic">Knoellia</span>.</p>
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<p>The number and functional gene classification of pan genomes between different <span class="html-italic">Knoellia</span> strains. The upset plot shows the number and functional classification of the core and unique genes in different <span class="html-italic">Knoellia</span> strains. The bar chart above represents the number of core and unique genes contained in each type of group. The strip at the bottom left represents the total number of genes in different <span class="html-italic">Knoellia</span> strains. The dot and line at the bottom right represent the types of different combinations (where only values above 10 and annotated genes are shown; further, unknown genes were not shown).</p>
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13 pages, 885 KiB  
Review
Haloarchaea as Promising Chassis to Green Chemistry
by Emma Bonnaud, Philippe M. Oger, Avigaël Ohayon and Yoann Louis
Microorganisms 2024, 12(8), 1738; https://doi.org/10.3390/microorganisms12081738 - 22 Aug 2024
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Abstract
Climate change and the scarcity of primary resources are driving the development of new, more renewable and environmentally friendly industrial processes. As part of this green chemistry approach, extremozymes (extreme microbial enzymes) can be used to replace all or part of the chemical [...] Read more.
Climate change and the scarcity of primary resources are driving the development of new, more renewable and environmentally friendly industrial processes. As part of this green chemistry approach, extremozymes (extreme microbial enzymes) can be used to replace all or part of the chemical synthesis stages of traditional industrial processes. At present, the production of these enzymes is limited by the cellular chassis available. The production of a large number of extremozymes requires extremophilic cellular chassis, which are not available. This is particularly true of halophilic extremozymes. The aim of this review is to present the current potential and challenges associated with the development of a haloarchaea-based cellular chassis. By overcoming the major obstacle of the limited number of genetic tools, it will be possible to propose a robust cellular chassis for the production of functional halophilic enzymes that can participate in the industrial transition of many sectors. Full article
(This article belongs to the Section Environmental Microbiology)
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Graphical abstract

Graphical abstract
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<p>Schematic illustration of the salt-out strategy adopted by some haloarchaea. Representation of the mechanisms of adaptation to high salinities. To cope with the high potential of these environments, two strategies can be adopted by halophilic archaea. The salt-out strategy is divided into two parts. It starts with an immediate adjustment response, consisting of the cellular import of K<sup>+</sup> (acute osmotic stress). The second phase starts with the import or de novo synthesis of the compatible solute [<a href="#B11-microorganisms-12-01738" class="html-bibr">11</a>]. During this phase, Na<sup>+</sup> and K<sup>+</sup> are excluded from the cytoplasm. Cells also have efflux systems for compatible solutes (turquoise transporter, which may adjust the turgor during allotment and doubling before cell division) and Msc channels (mechanosensitive channels, which serve as safety valves, allowing the rapid release of ions and organic solutes in the case of sudden downward osmotic shocks) [<a href="#B13-microorganisms-12-01738" class="html-bibr">13</a>]. The salt-in strategy is implemented by sequestering cations in the cytoplasm [<a href="#B12-microorganisms-12-01738" class="html-bibr">12</a>]. For this, Cl<sup>−</sup> is transported into the cytoplasm with the help of primary or secondary transporters (halorhodopsin, light-driven chloride pump in purple and symporter in blue), and potassium is absorbed with K<sup>+</sup> uniport (green transporter), driven by membrane potential [<a href="#B14-microorganisms-12-01738" class="html-bibr">14</a>]. Whatever the strategy, sodium ions are expelled from the cytoplasm by Na<sup>+</sup>/H<sup>+</sup> antiporters [<a href="#B9-microorganisms-12-01738" class="html-bibr">9</a>]. The most important transporters are summarized in this figure; they include ion pumps (e.g., Cl<sup>−</sup> pump in purple), uniport (K<sup>+</sup> uniport), antiporters (such as Na<sup>+</sup>/H<sup>+</sup> antiporter), bacteriorhodopsin (membrane bound proton pump), symporter (chloride transport probably coupled with inward transport of sodium), ATP synthase (ATP formation) and respiratory chain (proton translocation) [<a href="#B9-microorganisms-12-01738" class="html-bibr">9</a>]. The red and blue arrows represent the fluxes of water in ad out of the cell respectively.</p>
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<p>Haloarchaea chassis specification.</p>
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