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Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities

A multifunctional enzyme is one that performs multiple physiological functions, thus benefiting the organism. Characterization of multifunctional enzymes is important for researchers to understand how organisms adapt to different environmental challenges. In the present study, we report the discover...

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Detalles Bibliográficos
Autores principales: Liu, Ge, Wu, Shimei, Jin, Weihua, Sun, Chaomin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698717/
https://www.ncbi.nlm.nih.gov/pubmed/26725302
http://dx.doi.org/10.1038/srep18726
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author Liu, Ge
Wu, Shimei
Jin, Weihua
Sun, Chaomin
author_facet Liu, Ge
Wu, Shimei
Jin, Weihua
Sun, Chaomin
author_sort Liu, Ge
collection PubMed
description A multifunctional enzyme is one that performs multiple physiological functions, thus benefiting the organism. Characterization of multifunctional enzymes is important for researchers to understand how organisms adapt to different environmental challenges. In the present study, we report the discovery of a novel multifunctional enzyme Amy63 produced by marine bacterium Vibrio alginolyticus 63. Remarkably, Amy63 possesses amylase, agarase and carrageenase activities. Amy63 is a substrate promiscuous α-amylase, with the substrate priority order of starch, carrageenan and agar. Amy63 maintains considerable amylase, carrageenase and agarase activities and stabilities at wide temperature and pH ranges, and optimum activities are detected at temperature of 60 °C and pH of 6.0, respectively. Moreover, the heteroexpression of Amy63 dramatically enhances the ability of E. coli to degrade starch, carrageenan and agar. Motif searching shows three continuous glycosyl hydrolase 70 (GH70) family homologs existed in Amy63 encoding sequence. Combining serial deletions and phylogenetic analysis of Amy63, the GH70 homologs are proposed as the determinants of enzyme promiscuity. Notably, such enzymes exist in all kingdoms of life, thus providing an expanded perspective on studies of multifunctional enzymes. To our knowledge, this is the first report of an amylase having additional agarase and carrageenase activities.
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spelling pubmed-46987172016-01-13 Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities Liu, Ge Wu, Shimei Jin, Weihua Sun, Chaomin Sci Rep Article A multifunctional enzyme is one that performs multiple physiological functions, thus benefiting the organism. Characterization of multifunctional enzymes is important for researchers to understand how organisms adapt to different environmental challenges. In the present study, we report the discovery of a novel multifunctional enzyme Amy63 produced by marine bacterium Vibrio alginolyticus 63. Remarkably, Amy63 possesses amylase, agarase and carrageenase activities. Amy63 is a substrate promiscuous α-amylase, with the substrate priority order of starch, carrageenan and agar. Amy63 maintains considerable amylase, carrageenase and agarase activities and stabilities at wide temperature and pH ranges, and optimum activities are detected at temperature of 60 °C and pH of 6.0, respectively. Moreover, the heteroexpression of Amy63 dramatically enhances the ability of E. coli to degrade starch, carrageenan and agar. Motif searching shows three continuous glycosyl hydrolase 70 (GH70) family homologs existed in Amy63 encoding sequence. Combining serial deletions and phylogenetic analysis of Amy63, the GH70 homologs are proposed as the determinants of enzyme promiscuity. Notably, such enzymes exist in all kingdoms of life, thus providing an expanded perspective on studies of multifunctional enzymes. To our knowledge, this is the first report of an amylase having additional agarase and carrageenase activities. Nature Publishing Group 2016-01-04 /pmc/articles/PMC4698717/ /pubmed/26725302 http://dx.doi.org/10.1038/srep18726 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liu, Ge
Wu, Shimei
Jin, Weihua
Sun, Chaomin
Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title_full Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title_fullStr Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title_full_unstemmed Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title_short Amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
title_sort amy63, a novel type of marine bacterial multifunctional enzyme possessing amylase, agarase and carrageenase activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698717/
https://www.ncbi.nlm.nih.gov/pubmed/26725302
http://dx.doi.org/10.1038/srep18726
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