A modular system for Clostridium shuttle plasmids

被引:379
作者
Heap, John T. [1 ]
Pennington, Oliver J. [1 ]
Cartman, Stephen T. [1 ]
Minton, Nigel P. [1 ]
机构
[1] Univ Nottingham, BBSRC Sustainable BioEnergy Ctr, Sch Mol Med Sci, Ctr Biomol Sci, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
Clostridium; Plasmid; Shuttle; Vector; TRANSFERABLE TETRACYCLINE RESISTANCE; BACILLUS-SUBTILIS; ESCHERICHIA-COLI; REPORTER SYSTEM; ACETOBUTYLICUM; PERFRINGENS; GENE; VECTORS; CLONING; IDENTIFICATION;
D O I
10.1016/j.mimet.2009.05.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Despite their medical and industrial importance, our basic understanding of the biology of the genus Clostridium is rudimentary in comparison to their aerobic counterparts in the genus Bacillus. A major contributing factor has been the comparative lack of sophistication in the gene tools available to the clostridial molecular biologist, which are immature, and in clear need of development. The transfer and maintenance of recombinant, replicative plasmids into various species of Clostridium has been reported, and several elements suitable as shuttle plasmid components are known. However, these components have to-date only been available in disparate plasmid contexts, and their use has not been broadly explored. Here we describe the specification, design and construction of a standardized modular system for Clostridium-Escherichia coli shuttle plasmids. Existing replicons and selectable markers were incorporated, along with a novel clostridial replicon. The properties of these components were compared, and the data allow researchers to identify combinations of components potentially suitable for particular hosts and applications. The system has been extensively tested in our laboratory, where it is utilized in all ongoing recombinant work. We propose that adoption of this modular system as a standard would be of substantial benefit to the Clostridium research community, whom we invite to use and contribute to the system. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 85
页数:7
相关论文
共 41 条
[11]  
Davis TO, 2000, J MOL MICROB BIOTECH, V2, P59
[12]  
DAVIS TO, 1998, THESIS OPEN U
[13]   IDENTIFICATION AND MOLECULAR GENETIC-ANALYSIS OF REPLICATION FUNCTIONS OF THE BACTERIOCINOGENIC PLASMID PLP404 FROM CLOSTRIDIUM-PERFRINGENS [J].
GARNIER, T ;
COLE, ST .
PLASMID, 1988, 19 (02) :151-160
[14]   Development of a sensitive gene expression reporter system and an inducible promoter-repressor system for Clostridium acetobutylicum [J].
Girbal, L ;
Mortier-Barrière, I ;
Raynaud, F ;
Rouanet, C ;
Croux, C ;
Soucaille, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (08) :4985-4988
[15]   CLONING AND NUCLEOTIDE-SEQUENCE DETERMINATION OF THE CLOSTRIDIUM-PASTEURIANUM FERREDOXIN GENE [J].
GRAVES, MC ;
MULLENBACH, GT ;
RABINOWITZ, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (06) :1653-1657
[16]   INTERMEDIARY METABOLISM IN CLOSTRIDIUM-ACETOBUTYLICUM - LEVELS OF ENZYMES INVOLVED IN THE FORMATION OF ACETATE AND BUTYRATE [J].
HARTMANIS, MGN ;
GATENBECK, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1984, 47 (06) :1277-1283
[17]   TOXIGENIC CLOSTRIDIA [J].
HATHEWAY, CL .
CLINICAL MICROBIOLOGY REVIEWS, 1990, 3 (01) :66-98
[18]   The ClosTron:: A universal gene knock-out system for the genus Clostridium [J].
Heap, John T. ;
Pennington, Oliver J. ;
Cartman, Stephen T. ;
Carter, Glen P. ;
Minton, Nigel P. .
JOURNAL OF MICROBIOLOGICAL METHODS, 2007, 70 (03) :452-464
[19]   SITE-DIRECTED MUTAGENESIS BY OVERLAP EXTENSION USING THE POLYMERASE CHAIN-REACTION [J].
HO, SN ;
HUNT, HD ;
HORTON, RM ;
PULLEN, JK ;
PEASE, LR .
GENE, 1989, 77 (01) :51-59
[20]   Gene transfer to Clostridium cellulolyticum ATCC 35319 [J].
Jennert, KCB ;
Tardif, C ;
Young, DI ;
Young, M .
MICROBIOLOGY-SGM, 2000, 146 :3071-3080