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An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea

Microbial enzymes during solid-state fermentation (SSF), which play important roles in the food, chemical, pharmaceutical and environmental fields, remain relatively unknown. In this work, the microbial communities and enzymes in SSF of Pu-erh tea, a well-known traditional Chinese tea, were investig...

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Autores principales: Zhao, Ming, Zhang, Dong-lian, Su, Xiao-qin, Duan, Shuang-mei, Wan, Jin-qiong, Yuan, Wen-xia, Liu, Ben-ying, Ma, Yan, Pan, Ying-hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431464/
https://www.ncbi.nlm.nih.gov/pubmed/25974221
http://dx.doi.org/10.1038/srep10117
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author Zhao, Ming
Zhang, Dong-lian
Su, Xiao-qin
Duan, Shuang-mei
Wan, Jin-qiong
Yuan, Wen-xia
Liu, Ben-ying
Ma, Yan
Pan, Ying-hong
author_facet Zhao, Ming
Zhang, Dong-lian
Su, Xiao-qin
Duan, Shuang-mei
Wan, Jin-qiong
Yuan, Wen-xia
Liu, Ben-ying
Ma, Yan
Pan, Ying-hong
author_sort Zhao, Ming
collection PubMed
description Microbial enzymes during solid-state fermentation (SSF), which play important roles in the food, chemical, pharmaceutical and environmental fields, remain relatively unknown. In this work, the microbial communities and enzymes in SSF of Pu-erh tea, a well-known traditional Chinese tea, were investigated by integrated metagenomics/metaproteomics approach. The dominant bacteria and fungi were identified as Proteobacteria (48.42%) and Aspergillus (94.98%), through pyrosequencing-based analyses of the bacterial 16S and fungal 18S rRNA genes, respectively. In total, 335 proteins with at least two unique peptides were identified and classified into 28 Biological Processes and 35 Molecular Function categories using a metaproteomics analysis. The integration of metagenomics and metaproteomics data demonstrated that Aspergillus was dominant fungus and major host of identified proteins (50.45%). Enzymes involved in the degradation of the plant cell wall were identified and associated with the soft-rotting of tea leaves. Peroxiredoxins, catalase and peroxidases were associated with the oxidation of catechins. In conclusion, this work greatly advances our understanding of the SSF of Pu-erh tea and provides a powerful tool for studying SSF mechanisms, especially in relation to the microbial communities present.
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spelling pubmed-44314642015-05-22 An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea Zhao, Ming Zhang, Dong-lian Su, Xiao-qin Duan, Shuang-mei Wan, Jin-qiong Yuan, Wen-xia Liu, Ben-ying Ma, Yan Pan, Ying-hong Sci Rep Article Microbial enzymes during solid-state fermentation (SSF), which play important roles in the food, chemical, pharmaceutical and environmental fields, remain relatively unknown. In this work, the microbial communities and enzymes in SSF of Pu-erh tea, a well-known traditional Chinese tea, were investigated by integrated metagenomics/metaproteomics approach. The dominant bacteria and fungi were identified as Proteobacteria (48.42%) and Aspergillus (94.98%), through pyrosequencing-based analyses of the bacterial 16S and fungal 18S rRNA genes, respectively. In total, 335 proteins with at least two unique peptides were identified and classified into 28 Biological Processes and 35 Molecular Function categories using a metaproteomics analysis. The integration of metagenomics and metaproteomics data demonstrated that Aspergillus was dominant fungus and major host of identified proteins (50.45%). Enzymes involved in the degradation of the plant cell wall were identified and associated with the soft-rotting of tea leaves. Peroxiredoxins, catalase and peroxidases were associated with the oxidation of catechins. In conclusion, this work greatly advances our understanding of the SSF of Pu-erh tea and provides a powerful tool for studying SSF mechanisms, especially in relation to the microbial communities present. Nature Publishing Group 2015-05-14 /pmc/articles/PMC4431464/ /pubmed/25974221 http://dx.doi.org/10.1038/srep10117 Text en Copyright © 2015, 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
Zhao, Ming
Zhang, Dong-lian
Su, Xiao-qin
Duan, Shuang-mei
Wan, Jin-qiong
Yuan, Wen-xia
Liu, Ben-ying
Ma, Yan
Pan, Ying-hong
An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title_full An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title_fullStr An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title_full_unstemmed An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title_short An Integrated Metagenomics/Metaproteomics Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation of Pu-erh tea
title_sort integrated metagenomics/metaproteomics investigation of the microbial communities and enzymes in solid-state fermentation of pu-erh tea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431464/
https://www.ncbi.nlm.nih.gov/pubmed/25974221
http://dx.doi.org/10.1038/srep10117
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