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High activity CAZyme cassette for improving biomass degradation in thermophiles
BACKGROUND: Thermophilic microorganisms and their enzymes offer several advantages for industrial application over their mesophilic counterparts. For example, a hyperthermophilic anaerobe, Caldicellulosiruptor bescii, was recently isolated from hot springs in Kamchatka, Siberia, and shown to have ve...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793385/ https://www.ncbi.nlm.nih.gov/pubmed/29434665 http://dx.doi.org/10.1186/s13068-018-1014-2 |
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author | Brunecky, Roman Chung, Daehwan Sarai, Nicholas S. Hengge, Neal Russell, Jordan F. Young, Jenna Mittal, Ashutosh Pason, Patthra Vander Wall, Todd Michener, William Shollenberger, Todd Westpheling, Janet Himmel, Michael E. Bomble, Yannick J. |
author_facet | Brunecky, Roman Chung, Daehwan Sarai, Nicholas S. Hengge, Neal Russell, Jordan F. Young, Jenna Mittal, Ashutosh Pason, Patthra Vander Wall, Todd Michener, William Shollenberger, Todd Westpheling, Janet Himmel, Michael E. Bomble, Yannick J. |
author_sort | Brunecky, Roman |
collection | PubMed |
description | BACKGROUND: Thermophilic microorganisms and their enzymes offer several advantages for industrial application over their mesophilic counterparts. For example, a hyperthermophilic anaerobe, Caldicellulosiruptor bescii, was recently isolated from hot springs in Kamchatka, Siberia, and shown to have very high cellulolytic activity. Additionally, it is one of a few microorganisms being considered as viable candidates for consolidated bioprocessing applications. Moreover, C. bescii is capable of deconstructing plant biomass without enzymatic or chemical pretreatment. This ability is accomplished by the production and secretion of free, multi-modular and multi-functional enzymes, one of which, CbCel9A/Cel48A also known as CelA, is able to outperform enzymes found in commercial enzyme preparations. Furthermore, the complete C. bescii exoproteome is extremely thermostable and highly active at elevated temperatures, unlike commercial fungal cellulases. Therefore, understanding the functional diversity of enzymes in the C. bescii exoproteome and how inter-molecular synergy between them confers C. bescii with its high cellulolytic activity is an important endeavor to enable the production of more efficient biomass degrading enzyme formulations and in turn, better cellulolytic industrial microorganisms. RESULTS: To advance the understanding of the C. bescii exoproteome we have expressed, purified, and tested four of the primary enzymes found in the exoproteome and we have found that the combination of three or four of the most highly expressed enzymes exhibit synergistic activity. We also demonstrated that discrete combinations of these enzymes mimic and even improve upon the activity of the whole C. bescii exoproteome, even though some of the enzymes lack significant activity on their own. CONCLUSIONS: We have demonstrated that it is possible to replicate the cellulolytic activity of the native C. bescii exoproteome utilizing a minimal gene set, and that these minimal gene sets are more active than the whole exoproteome. In the future, this may lead to more simplified and efficient cellulolytic enzyme preparations or yield improvements when these enzymes are expressed in microorganisms engineered for consolidated bioprocessing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1014-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5793385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57933852018-02-12 High activity CAZyme cassette for improving biomass degradation in thermophiles Brunecky, Roman Chung, Daehwan Sarai, Nicholas S. Hengge, Neal Russell, Jordan F. Young, Jenna Mittal, Ashutosh Pason, Patthra Vander Wall, Todd Michener, William Shollenberger, Todd Westpheling, Janet Himmel, Michael E. Bomble, Yannick J. Biotechnol Biofuels Research BACKGROUND: Thermophilic microorganisms and their enzymes offer several advantages for industrial application over their mesophilic counterparts. For example, a hyperthermophilic anaerobe, Caldicellulosiruptor bescii, was recently isolated from hot springs in Kamchatka, Siberia, and shown to have very high cellulolytic activity. Additionally, it is one of a few microorganisms being considered as viable candidates for consolidated bioprocessing applications. Moreover, C. bescii is capable of deconstructing plant biomass without enzymatic or chemical pretreatment. This ability is accomplished by the production and secretion of free, multi-modular and multi-functional enzymes, one of which, CbCel9A/Cel48A also known as CelA, is able to outperform enzymes found in commercial enzyme preparations. Furthermore, the complete C. bescii exoproteome is extremely thermostable and highly active at elevated temperatures, unlike commercial fungal cellulases. Therefore, understanding the functional diversity of enzymes in the C. bescii exoproteome and how inter-molecular synergy between them confers C. bescii with its high cellulolytic activity is an important endeavor to enable the production of more efficient biomass degrading enzyme formulations and in turn, better cellulolytic industrial microorganisms. RESULTS: To advance the understanding of the C. bescii exoproteome we have expressed, purified, and tested four of the primary enzymes found in the exoproteome and we have found that the combination of three or four of the most highly expressed enzymes exhibit synergistic activity. We also demonstrated that discrete combinations of these enzymes mimic and even improve upon the activity of the whole C. bescii exoproteome, even though some of the enzymes lack significant activity on their own. CONCLUSIONS: We have demonstrated that it is possible to replicate the cellulolytic activity of the native C. bescii exoproteome utilizing a minimal gene set, and that these minimal gene sets are more active than the whole exoproteome. In the future, this may lead to more simplified and efficient cellulolytic enzyme preparations or yield improvements when these enzymes are expressed in microorganisms engineered for consolidated bioprocessing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1014-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-01 /pmc/articles/PMC5793385/ /pubmed/29434665 http://dx.doi.org/10.1186/s13068-018-1014-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Brunecky, Roman Chung, Daehwan Sarai, Nicholas S. Hengge, Neal Russell, Jordan F. Young, Jenna Mittal, Ashutosh Pason, Patthra Vander Wall, Todd Michener, William Shollenberger, Todd Westpheling, Janet Himmel, Michael E. Bomble, Yannick J. High activity CAZyme cassette for improving biomass degradation in thermophiles |
title | High activity CAZyme cassette for improving biomass degradation in thermophiles |
title_full | High activity CAZyme cassette for improving biomass degradation in thermophiles |
title_fullStr | High activity CAZyme cassette for improving biomass degradation in thermophiles |
title_full_unstemmed | High activity CAZyme cassette for improving biomass degradation in thermophiles |
title_short | High activity CAZyme cassette for improving biomass degradation in thermophiles |
title_sort | high activity cazyme cassette for improving biomass degradation in thermophiles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793385/ https://www.ncbi.nlm.nih.gov/pubmed/29434665 http://dx.doi.org/10.1186/s13068-018-1014-2 |
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