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Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids

Economically viable production of cellulosic biofuels requires operation at high solids loadings—on the order of 15 wt%. To this end we characterize Nature’s ability to deconstruct and utilize mid-season switchgrass at increasing solid loadings using an anaerobic methanogenic microbiome. This commun...

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Autores principales: Chirania, Payal, Holwerda, Evert K., Giannone, Richard J., Liang, Xiaoyu, Poudel, Suresh, Ellis, Joseph C., Bomble, Yannick J., Hettich, Robert L., Lynd, Lee R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256739/
https://www.ncbi.nlm.nih.gov/pubmed/35790765
http://dx.doi.org/10.1038/s41467-022-31433-x
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author Chirania, Payal
Holwerda, Evert K.
Giannone, Richard J.
Liang, Xiaoyu
Poudel, Suresh
Ellis, Joseph C.
Bomble, Yannick J.
Hettich, Robert L.
Lynd, Lee R.
author_facet Chirania, Payal
Holwerda, Evert K.
Giannone, Richard J.
Liang, Xiaoyu
Poudel, Suresh
Ellis, Joseph C.
Bomble, Yannick J.
Hettich, Robert L.
Lynd, Lee R.
author_sort Chirania, Payal
collection PubMed
description Economically viable production of cellulosic biofuels requires operation at high solids loadings—on the order of 15 wt%. To this end we characterize Nature’s ability to deconstruct and utilize mid-season switchgrass at increasing solid loadings using an anaerobic methanogenic microbiome. This community exhibits undiminished fractional carbohydrate solubilization at loadings ranging from 30 g/L to 150 g/L. Metaproteomic interrogation reveals marked increases in the abundance of specific carbohydrate-active enzyme classes. Significant enrichment of auxiliary activity family 6 enzymes at higher solids suggests a role for Fenton chemistry. Stress-response proteins accompanying these reactions are similarly upregulated at higher solids, as are β-glucosidases, xylosidases, carbohydrate-debranching, and pectin-acting enzymes—all of which indicate that removal of deconstruction inhibitors is important for observed undiminished solubilization. Our work provides insights into the mechanisms by which natural microbiomes effectively deconstruct and utilize lignocellulose at high solids loadings, informing the future development of defined cultures for efficient bioconversion.
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spelling pubmed-92567392022-07-07 Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids Chirania, Payal Holwerda, Evert K. Giannone, Richard J. Liang, Xiaoyu Poudel, Suresh Ellis, Joseph C. Bomble, Yannick J. Hettich, Robert L. Lynd, Lee R. Nat Commun Article Economically viable production of cellulosic biofuels requires operation at high solids loadings—on the order of 15 wt%. To this end we characterize Nature’s ability to deconstruct and utilize mid-season switchgrass at increasing solid loadings using an anaerobic methanogenic microbiome. This community exhibits undiminished fractional carbohydrate solubilization at loadings ranging from 30 g/L to 150 g/L. Metaproteomic interrogation reveals marked increases in the abundance of specific carbohydrate-active enzyme classes. Significant enrichment of auxiliary activity family 6 enzymes at higher solids suggests a role for Fenton chemistry. Stress-response proteins accompanying these reactions are similarly upregulated at higher solids, as are β-glucosidases, xylosidases, carbohydrate-debranching, and pectin-acting enzymes—all of which indicate that removal of deconstruction inhibitors is important for observed undiminished solubilization. Our work provides insights into the mechanisms by which natural microbiomes effectively deconstruct and utilize lignocellulose at high solids loadings, informing the future development of defined cultures for efficient bioconversion. Nature Publishing Group UK 2022-07-05 /pmc/articles/PMC9256739/ /pubmed/35790765 http://dx.doi.org/10.1038/s41467-022-31433-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chirania, Payal
Holwerda, Evert K.
Giannone, Richard J.
Liang, Xiaoyu
Poudel, Suresh
Ellis, Joseph C.
Bomble, Yannick J.
Hettich, Robert L.
Lynd, Lee R.
Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title_full Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title_fullStr Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title_full_unstemmed Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title_short Metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
title_sort metaproteomics reveals enzymatic strategies deployed by anaerobic microbiomes to maintain lignocellulose deconstruction at high solids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256739/
https://www.ncbi.nlm.nih.gov/pubmed/35790765
http://dx.doi.org/10.1038/s41467-022-31433-x
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