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The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation

A demonstration of cellulose degrading bacterium from human gut changed our view that human cannot degrade the cellulose. However, investigation of cellulose degradation by human gut microbiota on molecular level has not been completed so far. We showed here, using cellobiose as a model that promote...

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Autores principales: Li, Meixia, Wang, Yeqing, Guo, Ciliang, Wang, Sheng, Zheng, Liangzhen, Bu, Yifan, Ding, Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291918/
https://www.ncbi.nlm.nih.gov/pubmed/37349961
http://dx.doi.org/10.1080/19490976.2023.2227434
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author Li, Meixia
Wang, Yeqing
Guo, Ciliang
Wang, Sheng
Zheng, Liangzhen
Bu, Yifan
Ding, Kan
author_facet Li, Meixia
Wang, Yeqing
Guo, Ciliang
Wang, Sheng
Zheng, Liangzhen
Bu, Yifan
Ding, Kan
author_sort Li, Meixia
collection PubMed
description A demonstration of cellulose degrading bacterium from human gut changed our view that human cannot degrade the cellulose. However, investigation of cellulose degradation by human gut microbiota on molecular level has not been completed so far. We showed here, using cellobiose as a model that promoted the growth of human gut key members, such as Bacteroides ovatus (BO), to clarify the molecular mechanism. Our results showed that a new polysaccharide utilization locus (PUL) from BO was involved in the cellobiose capturing and degradation. Further, two new cellulases BACOVA_02626(GH5) and BACOVA_02630(GH5) on the cell surface performed the degradation of cellobiose into glucose were determined. The predicted structures of BACOVA_02626(GH5) and BACOVA_02630(GH5) were highly homologous with the cellulase from soil bacteria, and the catalytic residues were highly conservative with two glutamate residues. In murine experiment, we observed cellobiose reshaped the composition of gut microbiota and probably modified the metabolic function of bacteria. Taken together, our findings further highlight the evidence of cellulose can be degraded by human gut microbes and provide new insight in the field of investigation on cellulose.
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spelling pubmed-102919182023-06-27 The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation Li, Meixia Wang, Yeqing Guo, Ciliang Wang, Sheng Zheng, Liangzhen Bu, Yifan Ding, Kan Gut Microbes Research Paper A demonstration of cellulose degrading bacterium from human gut changed our view that human cannot degrade the cellulose. However, investigation of cellulose degradation by human gut microbiota on molecular level has not been completed so far. We showed here, using cellobiose as a model that promoted the growth of human gut key members, such as Bacteroides ovatus (BO), to clarify the molecular mechanism. Our results showed that a new polysaccharide utilization locus (PUL) from BO was involved in the cellobiose capturing and degradation. Further, two new cellulases BACOVA_02626(GH5) and BACOVA_02630(GH5) on the cell surface performed the degradation of cellobiose into glucose were determined. The predicted structures of BACOVA_02626(GH5) and BACOVA_02630(GH5) were highly homologous with the cellulase from soil bacteria, and the catalytic residues were highly conservative with two glutamate residues. In murine experiment, we observed cellobiose reshaped the composition of gut microbiota and probably modified the metabolic function of bacteria. Taken together, our findings further highlight the evidence of cellulose can be degraded by human gut microbes and provide new insight in the field of investigation on cellulose. Taylor & Francis 2023-06-22 /pmc/articles/PMC10291918/ /pubmed/37349961 http://dx.doi.org/10.1080/19490976.2023.2227434 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Li, Meixia
Wang, Yeqing
Guo, Ciliang
Wang, Sheng
Zheng, Liangzhen
Bu, Yifan
Ding, Kan
The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title_full The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title_fullStr The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title_full_unstemmed The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title_short The claim of primacy of human gut Bacteroides ovatus in dietary cellobiose degradation
title_sort claim of primacy of human gut bacteroides ovatus in dietary cellobiose degradation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291918/
https://www.ncbi.nlm.nih.gov/pubmed/37349961
http://dx.doi.org/10.1080/19490976.2023.2227434
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