产气荚膜梭菌
质粒
氯霉素乙酰转移酶
生物
穿梭机载体
多克隆站点
基因
大肠杆菌
克隆(编程)
克隆载体
载体(分子生物学)
报告基因
发起人
微生物学
分子生物学
遗传学
重组DNA
基因表达
细菌
程序设计语言
计算机科学
作者
Chieko Matsushita,Osamu Matsushita,Mamoru Koyama,Akinobu Okabe
出处
期刊:Plasmid
[Elsevier BV]
日期:1994-05-01
卷期号:31 (3): 317-319
被引量:35
标识
DOI:10.1006/plas.1994.1035
摘要
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 a useful reporter system for C. perfringens genes.
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