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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...

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Autores principales: Artzi, Lior, Dassa, Bareket, Borovok, Ilya, Shamshoum, Melina, Lamed, Raphael, Bayer, Edward A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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