Cargando…

Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum

Clostridium saccharoperbutylacetonicum is a mesophilic, anaerobic, butanol-producing bacterium, originally isolated from soil. It was recently reported that C. saccharoperbutylacetonicum possesses multiple cellulosomal elements and would potentially form the smallest cellulosome known in nature. Its...

Descripción completa

Detalles Bibliográficos
Autores principales: Levi Hevroni, Bosmat, Moraïs, Sarah, Ben-David, Yonit, Morag, Ely, Bayer, Edward A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157769/
https://www.ncbi.nlm.nih.gov/pubmed/32234813
http://dx.doi.org/10.1128/mBio.00443-20
_version_ 1783522418047844352
author Levi Hevroni, Bosmat
Moraïs, Sarah
Ben-David, Yonit
Morag, Ely
Bayer, Edward A.
author_facet Levi Hevroni, Bosmat
Moraïs, Sarah
Ben-David, Yonit
Morag, Ely
Bayer, Edward A.
author_sort Levi Hevroni, Bosmat
collection PubMed
description Clostridium saccharoperbutylacetonicum is a mesophilic, anaerobic, butanol-producing bacterium, originally isolated from soil. It was recently reported that C. saccharoperbutylacetonicum possesses multiple cellulosomal elements and would potentially form the smallest cellulosome known in nature. Its genome contains only eight dockerin-bearing enzymes, and its unique scaffoldin bears two cohesins (Cohs), three X2 modules, and two carbohydrate-binding modules (CBMs). In this study, all of the cellulosome-related modules were cloned, expressed, and purified. The recombinant cohesins, dockerins, and CBMs were tested for binding activity using enzyme-linked immunosorbent assay (ELISA)-based techniques. All the enzymes were tested for their comparative enzymatic activity on seven different cellulosic and hemicellulosic substrates, thus revealing four cellulases, a xylanase, a mannanase, a xyloglucanase, and a lichenase. All dockerin-containing enzymes interacted similarly with the second cohesin (Coh2) module, whereas Coh1 was more restricted in its interaction pattern. In addition, the polysaccharide-binding properties of the CBMs within the scaffoldin were examined by two complementary assays, affinity electrophoresis and affinity pulldown. The scaffoldin of C. saccharoperbutylacetonicum exhibited high affinity for cellulosic and hemicellulosic substrates, specifically to microcrystalline cellulose and xyloglucan. Evidence that supports substrate-dependent in vivo secretion of cellulosomes is presented. The results of our analyses contribute to a better understanding of simple cellulosome systems by identifying the key players in this minimalistic system and the binding pattern of its cohesin-dockerin interaction. The knowledge gained by our study will assist further exploration of similar minimalistic cellulosomes and will contribute to the significance of specific sets of defined cellulosomal enzymes in the degradation of cellulosic biomass.
format Online
Article
Text
id pubmed-7157769
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-71577692020-04-15 Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum Levi Hevroni, Bosmat Moraïs, Sarah Ben-David, Yonit Morag, Ely Bayer, Edward A. mBio Research Article Clostridium saccharoperbutylacetonicum is a mesophilic, anaerobic, butanol-producing bacterium, originally isolated from soil. It was recently reported that C. saccharoperbutylacetonicum possesses multiple cellulosomal elements and would potentially form the smallest cellulosome known in nature. Its genome contains only eight dockerin-bearing enzymes, and its unique scaffoldin bears two cohesins (Cohs), three X2 modules, and two carbohydrate-binding modules (CBMs). In this study, all of the cellulosome-related modules were cloned, expressed, and purified. The recombinant cohesins, dockerins, and CBMs were tested for binding activity using enzyme-linked immunosorbent assay (ELISA)-based techniques. All the enzymes were tested for their comparative enzymatic activity on seven different cellulosic and hemicellulosic substrates, thus revealing four cellulases, a xylanase, a mannanase, a xyloglucanase, and a lichenase. All dockerin-containing enzymes interacted similarly with the second cohesin (Coh2) module, whereas Coh1 was more restricted in its interaction pattern. In addition, the polysaccharide-binding properties of the CBMs within the scaffoldin were examined by two complementary assays, affinity electrophoresis and affinity pulldown. The scaffoldin of C. saccharoperbutylacetonicum exhibited high affinity for cellulosic and hemicellulosic substrates, specifically to microcrystalline cellulose and xyloglucan. Evidence that supports substrate-dependent in vivo secretion of cellulosomes is presented. The results of our analyses contribute to a better understanding of simple cellulosome systems by identifying the key players in this minimalistic system and the binding pattern of its cohesin-dockerin interaction. The knowledge gained by our study will assist further exploration of similar minimalistic cellulosomes and will contribute to the significance of specific sets of defined cellulosomal enzymes in the degradation of cellulosic biomass. American Society for Microbiology 2020-03-31 /pmc/articles/PMC7157769/ /pubmed/32234813 http://dx.doi.org/10.1128/mBio.00443-20 Text en Copyright © 2020 Levi Hevroni et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Levi Hevroni, Bosmat
Moraïs, Sarah
Ben-David, Yonit
Morag, Ely
Bayer, Edward A.
Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title_full Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title_fullStr Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title_full_unstemmed Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title_short Minimalistic Cellulosome of the Butanologenic Bacterium Clostridium saccharoperbutylacetonicum
title_sort minimalistic cellulosome of the butanologenic bacterium clostridium saccharoperbutylacetonicum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157769/
https://www.ncbi.nlm.nih.gov/pubmed/32234813
http://dx.doi.org/10.1128/mBio.00443-20
work_keys_str_mv AT levihevronibosmat minimalisticcellulosomeofthebutanologenicbacteriumclostridiumsaccharoperbutylacetonicum
AT moraissarah minimalisticcellulosomeofthebutanologenicbacteriumclostridiumsaccharoperbutylacetonicum
AT bendavidyonit minimalisticcellulosomeofthebutanologenicbacteriumclostridiumsaccharoperbutylacetonicum
AT moragely minimalisticcellulosomeofthebutanologenicbacteriumclostridiumsaccharoperbutylacetonicum
AT bayeredwarda minimalisticcellulosomeofthebutanologenicbacteriumclostridiumsaccharoperbutylacetonicum