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Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid

Treatment with rumen fluid improves methane production from non‐degradable lignocellulosic biomass during subsequent methane fermentation; however, the kinetics of xylanases during treatment with rumen fluid remain unclear. This study aimed to identify key xylanases contributing to xylan degradation...

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Autores principales: Takizawa, Shuhei, Asano, Ryoki, Fukuda, Yasuhiro, Baba, Yasunori, Tada, Chika, Nakai, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151333/
https://www.ncbi.nlm.nih.gov/pubmed/34964273
http://dx.doi.org/10.1111/1751-7915.13988
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author Takizawa, Shuhei
Asano, Ryoki
Fukuda, Yasuhiro
Baba, Yasunori
Tada, Chika
Nakai, Yutaka
author_facet Takizawa, Shuhei
Asano, Ryoki
Fukuda, Yasuhiro
Baba, Yasunori
Tada, Chika
Nakai, Yutaka
author_sort Takizawa, Shuhei
collection PubMed
description Treatment with rumen fluid improves methane production from non‐degradable lignocellulosic biomass during subsequent methane fermentation; however, the kinetics of xylanases during treatment with rumen fluid remain unclear. This study aimed to identify key xylanases contributing to xylan degradation and their individual activities during xylan treatment with bovine rumen microorganisms. Xylan was treated with bovine rumen fluid at 37°C for 48 h under anaerobic conditions. Total solids were degraded into volatile fatty acids and gases during the first 24 h. Zymography showed that xylanases of 24, 34, 85, 180, and 200 kDa were highly active during the first 24 h. Therefore, these xylanases are considered to be crucial for xylan degradation during treatment with rumen fluid. Metagenomic analysis revealed that the rumen microbial community’s structure and metabolic function temporally shifted during xylan biodegradation. Although statistical analyses did not reveal significantly positive correlations between xylanase activities and known xylanolytic bacterial genera, they positively correlated with protozoal (e.g., Entodinium, Diploplastron, and Eudiplodinium) and fungal (e.g., Neocallimastix, Orpinomyces, and Olpidium) genera and unclassified bacteria. Our findings suggest that rumen protozoa, fungi, and unclassified bacteria are associated with key xylanase activities, accelerating xylan biodegradation into volatile fatty acids and gases, during treatment of lignocellulosic biomass with rumen fluid.
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spelling pubmed-91513332022-06-04 Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid Takizawa, Shuhei Asano, Ryoki Fukuda, Yasuhiro Baba, Yasunori Tada, Chika Nakai, Yutaka Microb Biotechnol Minireviews Treatment with rumen fluid improves methane production from non‐degradable lignocellulosic biomass during subsequent methane fermentation; however, the kinetics of xylanases during treatment with rumen fluid remain unclear. This study aimed to identify key xylanases contributing to xylan degradation and their individual activities during xylan treatment with bovine rumen microorganisms. Xylan was treated with bovine rumen fluid at 37°C for 48 h under anaerobic conditions. Total solids were degraded into volatile fatty acids and gases during the first 24 h. Zymography showed that xylanases of 24, 34, 85, 180, and 200 kDa were highly active during the first 24 h. Therefore, these xylanases are considered to be crucial for xylan degradation during treatment with rumen fluid. Metagenomic analysis revealed that the rumen microbial community’s structure and metabolic function temporally shifted during xylan biodegradation. Although statistical analyses did not reveal significantly positive correlations between xylanase activities and known xylanolytic bacterial genera, they positively correlated with protozoal (e.g., Entodinium, Diploplastron, and Eudiplodinium) and fungal (e.g., Neocallimastix, Orpinomyces, and Olpidium) genera and unclassified bacteria. Our findings suggest that rumen protozoa, fungi, and unclassified bacteria are associated with key xylanase activities, accelerating xylan biodegradation into volatile fatty acids and gases, during treatment of lignocellulosic biomass with rumen fluid. John Wiley and Sons Inc. 2021-12-28 /pmc/articles/PMC9151333/ /pubmed/34964273 http://dx.doi.org/10.1111/1751-7915.13988 Text en © 2021 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Minireviews
Takizawa, Shuhei
Asano, Ryoki
Fukuda, Yasuhiro
Baba, Yasunori
Tada, Chika
Nakai, Yutaka
Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title_full Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title_fullStr Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title_full_unstemmed Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title_short Shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
title_sort shifts in xylanases and the microbial community associated with xylan biodegradation during treatment with rumen fluid
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151333/
https://www.ncbi.nlm.nih.gov/pubmed/34964273
http://dx.doi.org/10.1111/1751-7915.13988
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