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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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.
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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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