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Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera
Thraustochytrids are heterotrophic fungus-like protists that can dissolve organic matters with enzymes. Four strains, AP45, ASP1, ASP2, and ASP4, were isolated from the coastal water of Taiwan, and respectively identified as Aurantiochytrium sp., Schizochytrium sp., Parietichytrium sp., and Botryoch...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641610/ https://www.ncbi.nlm.nih.gov/pubmed/33193181 http://dx.doi.org/10.3389/fmicb.2020.573907 |
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author | Lin, Hsiu-Chin Li, Wei-Hao Chen, Chi-Chih Cheng, Tien-Hsing Lan, Yu-Hsuan Huang, Ming-Der Chen, Wen-Ming Chang, Jo-Shu Chang, Hsin-Yang |
author_facet | Lin, Hsiu-Chin Li, Wei-Hao Chen, Chi-Chih Cheng, Tien-Hsing Lan, Yu-Hsuan Huang, Ming-Der Chen, Wen-Ming Chang, Jo-Shu Chang, Hsin-Yang |
author_sort | Lin, Hsiu-Chin |
collection | PubMed |
description | Thraustochytrids are heterotrophic fungus-like protists that can dissolve organic matters with enzymes. Four strains, AP45, ASP1, ASP2, and ASP4, were isolated from the coastal water of Taiwan, and respectively identified as Aurantiochytrium sp., Schizochytrium sp., Parietichytrium sp., and Botryochytrium sp. based on 18S rRNA sequences. Transcriptome datasets of these four strains at days 3-5 were generated using Next Generation Sequencing technology, and screened for enzymes with potential industrial applications. Functional annotations based on KEGG database suggest that many unigenes of all four strains were related to the pathways of industrial enzymes. Most of all four strains contained homologous genes for 15 out of the 17 targeted enzymes, and had extra- and/or intra-cellular enzymatic activities, including urease, asparaginase, lipase, glucosidase, alkaline phosphatase and protease. Complete amino sequences of the first-time identified L-asparaginase and phytase in thraustochytrids were retrieved, and respectively categorized to the Type I and BPPhy families based on phylogenetic relationships, protein structural modeling and active sites. Milligram quantities of highly purified, soluble protein of urease and L-asparaginase were successfully harvested and analyzed for recombinant enzymatic activities. These analytical results highlight the diverse enzymes for wide-range applications in thraustochytrids. |
format | Online Article Text |
id | pubmed-7641610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76416102020-11-13 Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera Lin, Hsiu-Chin Li, Wei-Hao Chen, Chi-Chih Cheng, Tien-Hsing Lan, Yu-Hsuan Huang, Ming-Der Chen, Wen-Ming Chang, Jo-Shu Chang, Hsin-Yang Front Microbiol Microbiology Thraustochytrids are heterotrophic fungus-like protists that can dissolve organic matters with enzymes. Four strains, AP45, ASP1, ASP2, and ASP4, were isolated from the coastal water of Taiwan, and respectively identified as Aurantiochytrium sp., Schizochytrium sp., Parietichytrium sp., and Botryochytrium sp. based on 18S rRNA sequences. Transcriptome datasets of these four strains at days 3-5 were generated using Next Generation Sequencing technology, and screened for enzymes with potential industrial applications. Functional annotations based on KEGG database suggest that many unigenes of all four strains were related to the pathways of industrial enzymes. Most of all four strains contained homologous genes for 15 out of the 17 targeted enzymes, and had extra- and/or intra-cellular enzymatic activities, including urease, asparaginase, lipase, glucosidase, alkaline phosphatase and protease. Complete amino sequences of the first-time identified L-asparaginase and phytase in thraustochytrids were retrieved, and respectively categorized to the Type I and BPPhy families based on phylogenetic relationships, protein structural modeling and active sites. Milligram quantities of highly purified, soluble protein of urease and L-asparaginase were successfully harvested and analyzed for recombinant enzymatic activities. These analytical results highlight the diverse enzymes for wide-range applications in thraustochytrids. Frontiers Media S.A. 2020-10-20 /pmc/articles/PMC7641610/ /pubmed/33193181 http://dx.doi.org/10.3389/fmicb.2020.573907 Text en Copyright © 2020 Lin, Li, Chen, Cheng, Lan, Huang, Chen, Chang and Chang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Lin, Hsiu-Chin Li, Wei-Hao Chen, Chi-Chih Cheng, Tien-Hsing Lan, Yu-Hsuan Huang, Ming-Der Chen, Wen-Ming Chang, Jo-Shu Chang, Hsin-Yang Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title | Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title_full | Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title_fullStr | Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title_full_unstemmed | Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title_short | Diverse Enzymes With Industrial Applications in Four Thraustochytrid Genera |
title_sort | diverse enzymes with industrial applications in four thraustochytrid genera |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641610/ https://www.ncbi.nlm.nih.gov/pubmed/33193181 http://dx.doi.org/10.3389/fmicb.2020.573907 |
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