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PMID: 8058826 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A Clostridium perfringens vector for the selection of promoters.

Plasmid ·Vol. 31 ·No. 3 ·1994-05-00 ·Pages 317-9

Matsushita C, Matsushita O, Koyama M, Okabe A

Abstract

A promoter selection vector for Clostridium perfringens genes was constructed from a C. perfringens-Escherichia coli shuttle vector, pJIR418. The plasmid carries a promoterless chloramphenicol acetyltransferase gene (catP), derived from pIP401, downstream of the multiple cloning sites of pUC18. When a promoter region of the phospholipase C gene was inserted into one of the cloning sites, derivatives of C. perfringens strain 13 carrying the resultant plasmid acquired resistance to chloramphenicol. This plasmid should be useful reporter system for C. perfringens genes.

Related Genes
MeSH Terms
Base Sequence Blotting, Northern Chloramphenicol O-Acetyltransferase/biosynthesis,genetics,metabolism Cloning, Molecular/methods Clostridium perfringens/genetics DNA Primers Escherichia coli Genes, Bacterial Genetic Vectors Molecular Sequence Data Plasmids Promoter Regions, Genetic RNA, Messenger/analysis,biosynthesis Restriction Mapping
Chemicals
DNA Primers RNA, Messenger Chloramphenicol O-Acetyltransferase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Matsushita C
Department of Microbiology, Kagawa Medical School, Japan.
Matsushita O
Koyama M
Okabe A
Article Info
Journal
Plasmid
Abbr.
Plasmid
ISSN
0147-619X
Published
1994-05-00
Pages
317-9
Language
English
Region
United States
NLM ID
7802221
Subset
IM
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