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Oxidative cleavage of cellulose in the horse gut

BACKGROUND: Lytic polysaccharide monooxygenases (LPMOs) belonging to the auxiliary activity 9 family (AA9) are widely found in aerobic fungi. These enzymes are O(2)-dependent copper oxidoreductases that catalyze the oxidative cleavage of cellulose. However, studies that have investigated AA9 LPMOs o...

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Autores principales: Liu, Ning, Yu, Weishuai, Guo, Xiuna, Chen, Jinyin, Xia, Donghui, Yu, Jie, Li, Duochuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917663/
https://www.ncbi.nlm.nih.gov/pubmed/35279161
http://dx.doi.org/10.1186/s12934-022-01767-8
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author Liu, Ning
Yu, Weishuai
Guo, Xiuna
Chen, Jinyin
Xia, Donghui
Yu, Jie
Li, Duochuan
author_facet Liu, Ning
Yu, Weishuai
Guo, Xiuna
Chen, Jinyin
Xia, Donghui
Yu, Jie
Li, Duochuan
author_sort Liu, Ning
collection PubMed
description BACKGROUND: Lytic polysaccharide monooxygenases (LPMOs) belonging to the auxiliary activity 9 family (AA9) are widely found in aerobic fungi. These enzymes are O(2)-dependent copper oxidoreductases that catalyze the oxidative cleavage of cellulose. However, studies that have investigated AA9 LPMOs of aerobic fungi in the herbivore gut are scare. To date, whether oxidative cleavage of cellulose occurs in the herbivore gut is unknown. RESULTS: We report for the first time experimental evidence that AA9 LPMOs from aerobic thermophilic fungi catalyze the oxidative cleavage of cellulose present in the horse gut to C1-oxidized cellulose and C1- and C4-oxidized cello-oligosaccharides. We isolated and identified three thermophilic fungi and measured their growth and AA9 LPMO expression at 37 °C in vitro. We also assessed the expression and the presence of AA9 LPMOs from thermophilic fungi in situ. Finally, we used two recombinant AA9 LPMOs and a native AA9 LPMO from thermophilic fungi to cleave cellulose to yield C1-oxidized products at 37 °C in vitro. CONCLUSIONS: The oxidative cleavage of cellulose occurs in the horse gut. This finding will broaden the known the biological functions of the ubiquitous LPMOs and aid in determining biological significance of aerobic thermophilic fungi. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01767-8.
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spelling pubmed-89176632022-03-21 Oxidative cleavage of cellulose in the horse gut Liu, Ning Yu, Weishuai Guo, Xiuna Chen, Jinyin Xia, Donghui Yu, Jie Li, Duochuan Microb Cell Fact Research BACKGROUND: Lytic polysaccharide monooxygenases (LPMOs) belonging to the auxiliary activity 9 family (AA9) are widely found in aerobic fungi. These enzymes are O(2)-dependent copper oxidoreductases that catalyze the oxidative cleavage of cellulose. However, studies that have investigated AA9 LPMOs of aerobic fungi in the herbivore gut are scare. To date, whether oxidative cleavage of cellulose occurs in the herbivore gut is unknown. RESULTS: We report for the first time experimental evidence that AA9 LPMOs from aerobic thermophilic fungi catalyze the oxidative cleavage of cellulose present in the horse gut to C1-oxidized cellulose and C1- and C4-oxidized cello-oligosaccharides. We isolated and identified three thermophilic fungi and measured their growth and AA9 LPMO expression at 37 °C in vitro. We also assessed the expression and the presence of AA9 LPMOs from thermophilic fungi in situ. Finally, we used two recombinant AA9 LPMOs and a native AA9 LPMO from thermophilic fungi to cleave cellulose to yield C1-oxidized products at 37 °C in vitro. CONCLUSIONS: The oxidative cleavage of cellulose occurs in the horse gut. This finding will broaden the known the biological functions of the ubiquitous LPMOs and aid in determining biological significance of aerobic thermophilic fungi. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01767-8. BioMed Central 2022-03-12 /pmc/articles/PMC8917663/ /pubmed/35279161 http://dx.doi.org/10.1186/s12934-022-01767-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Ning
Yu, Weishuai
Guo, Xiuna
Chen, Jinyin
Xia, Donghui
Yu, Jie
Li, Duochuan
Oxidative cleavage of cellulose in the horse gut
title Oxidative cleavage of cellulose in the horse gut
title_full Oxidative cleavage of cellulose in the horse gut
title_fullStr Oxidative cleavage of cellulose in the horse gut
title_full_unstemmed Oxidative cleavage of cellulose in the horse gut
title_short Oxidative cleavage of cellulose in the horse gut
title_sort oxidative cleavage of cellulose in the horse gut
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917663/
https://www.ncbi.nlm.nih.gov/pubmed/35279161
http://dx.doi.org/10.1186/s12934-022-01767-8
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