Matsushita C, Matsushita O, Koyama M, Okabe A
Department of Microbiology, Kagawa Medical School, Japan.
Plasmid. 1994 May;31(3):317-9. doi: 10.1006/plas.1994.1035.
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.
产气荚膜梭菌基因启动子选择载体是由产气荚膜梭菌-大肠杆菌穿梭载体pJIR418构建而成。该质粒携带一个无启动子的氯霉素乙酰转移酶基因(catP),它来源于pIP401,位于pUC18多克隆位点的下游。当将磷脂酶C基因的启动子区域插入其中一个克隆位点时,携带所得质粒的产气荚膜梭菌13菌株衍生物获得了对氯霉素的抗性。该质粒应是用于产气荚膜梭菌基因的有用报告系统。