Cellulosomics of the cellulolytic thermophile Clostridium clariflavum

被引:56
作者
Artzi, Lior [1 ]
Dassa, Bareket [1 ]
Borovok, Ilya [2 ]
Shamshoum, Melina [1 ]
Lamed, Raphael [2 ]
Bayer, Edward A. [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
[2] Tel Aviv Univ, Dept Mol Microbiol & Biotechnol, Ramat Aviv, Israel
基金
以色列科学基金会;
关键词
Cellulosomes; Cellulases; Cohesin; Dockerin; Scaffoldin; CBM; Glycoside hydrolases; Biomass degradation; Biofuels; COHESIN-DOCKERIN INTERACTION; CARBOHYDRATE-BINDING MODULES; ACETIVIBRIO-CELLULOLYTICUS; SEQUENCE-ANALYSIS; THERMOCELLUM; PROTEIN; DOMAIN; SCAFFOLDIN; COMPONENTS; CELLULASE;
D O I
10.1186/1754-6834-7-100
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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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页数:13
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