Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1784741198164918272 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9256739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chiraniapayal metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT holwerdaevertk metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT giannonerichardj metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT liangxiaoyu metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT poudelsuresh metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT ellisjosephc metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT bombleyannickj metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT hettichrobertl metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids AT lyndleer metaproteomicsrevealsenzymaticstrategiesdeployedbyanaerobicmicrobiomestomaintainlignocellulosedeconstructionathighsolids |