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Cellulosomics of the cellulolytic thermophile Clostridium clariflavum
BACKGROUND: Clostridium clariflavum is an anaerobic, thermophilic, Gram-positive bacterium, capable of growth on crystalline cellulose as a single carbon source. The genome of C. clariflavum has been sequenced to completion, and numerous cellulosomal genes were identified, including putative scaffol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582956/ https://www.ncbi.nlm.nih.gov/pubmed/26413154 http://dx.doi.org/10.1186/1754-6834-7-100 |
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author | Artzi, Lior Dassa, Bareket Borovok, Ilya Shamshoum, Melina Lamed, Raphael Bayer, Edward A |
author_facet | Artzi, Lior Dassa, Bareket Borovok, Ilya Shamshoum, Melina Lamed, Raphael Bayer, Edward A |
author_sort | Artzi, Lior |
collection | PubMed |
description | BACKGROUND: Clostridium clariflavum is an anaerobic, thermophilic, Gram-positive bacterium, capable of growth on crystalline cellulose as a single carbon source. The genome of C. clariflavum has been sequenced to completion, and numerous cellulosomal genes were identified, including putative scaffoldin and enzyme subunits. RESULTS: Bioinformatic analysis of the C. clariflavum genome revealed 49 cohesin modules distributed on 13 different scaffoldins and 79 dockerin-containing proteins, suggesting an abundance of putative cellulosome assemblies. The 13-scaffoldin system of C. clariflavum is highly reminiscent of the proposed cellulosome system of Acetivibrio cellulolyticus. Analysis of the C. clariflavum type I dockerin sequences indicated a very high level of conservation, wherein the putative recognition residues are remarkably similar to those of A. cellulolyticus. The numerous interactions among the cellulosomal components were elucidated using a standardized affinity ELISA-based fusion-protein system. The results revealed a rather simplistic recognition pattern of cohesin-dockerin interaction, whereby the type I and type II cohesins generally recognized the dockerins of the same type. The anticipated exception to this rule was the type I dockerin of the ScaB adaptor scaffoldin which bound selectively to the type I cohesins of ScaC and ScaJ. CONCLUSIONS: The findings reveal an intricate picture of predicted cellulosome assemblies in C. clariflavum. The network of cohesin-dockerin pairs provides a thermophilic alternative to those of C. thermocellum and a basis for subsequent utilization of the C. clariflavum cellulosomal system for biotechnological application. |
format | Online Article Text |
id | pubmed-4582956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45829562015-09-26 Cellulosomics of the cellulolytic thermophile Clostridium clariflavum Artzi, Lior Dassa, Bareket Borovok, Ilya Shamshoum, Melina Lamed, Raphael Bayer, Edward A Biotechnol Biofuels Research BACKGROUND: Clostridium clariflavum is an anaerobic, thermophilic, Gram-positive bacterium, capable of growth on crystalline cellulose as a single carbon source. The genome of C. clariflavum has been sequenced to completion, and numerous cellulosomal genes were identified, including putative scaffoldin and enzyme subunits. RESULTS: Bioinformatic analysis of the C. clariflavum genome revealed 49 cohesin modules distributed on 13 different scaffoldins and 79 dockerin-containing proteins, suggesting an abundance of putative cellulosome assemblies. The 13-scaffoldin system of C. clariflavum is highly reminiscent of the proposed cellulosome system of Acetivibrio cellulolyticus. Analysis of the C. clariflavum type I dockerin sequences indicated a very high level of conservation, wherein the putative recognition residues are remarkably similar to those of A. cellulolyticus. The numerous interactions among the cellulosomal components were elucidated using a standardized affinity ELISA-based fusion-protein system. The results revealed a rather simplistic recognition pattern of cohesin-dockerin interaction, whereby the type I and type II cohesins generally recognized the dockerins of the same type. The anticipated exception to this rule was the type I dockerin of the ScaB adaptor scaffoldin which bound selectively to the type I cohesins of ScaC and ScaJ. CONCLUSIONS: The findings reveal an intricate picture of predicted cellulosome assemblies in C. clariflavum. The network of cohesin-dockerin pairs provides a thermophilic alternative to those of C. thermocellum and a basis for subsequent utilization of the C. clariflavum cellulosomal system for biotechnological application. BioMed Central 2014-07-01 /pmc/articles/PMC4582956/ /pubmed/26413154 http://dx.doi.org/10.1186/1754-6834-7-100 Text en Copyright © 2014 Artzi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Artzi, Lior Dassa, Bareket Borovok, Ilya Shamshoum, Melina Lamed, Raphael Bayer, Edward A Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title | Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title_full | Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title_fullStr | Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title_full_unstemmed | Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title_short | Cellulosomics of the cellulolytic thermophile Clostridium clariflavum |
title_sort | cellulosomics of the cellulolytic thermophile clostridium clariflavum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582956/ https://www.ncbi.nlm.nih.gov/pubmed/26413154 http://dx.doi.org/10.1186/1754-6834-7-100 |
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