Wang Z, Xiong G, Lutz F
Institut für Pharmakologie und Toxikologie, Justus-Liebig-Universität Giessen, Germany.
Mol Gen Genet. 1995 Jan 6;246(1):72-9. doi: 10.1007/BF00290135.
The site-specific integration of the phage phi CTX genome, which carries the gene for a pore-forming cytotoxin, into the Pseudomonas aeruginosa chromosome was analysed. The 1,167 bp integrase gene, int, located immediately upstream of the attachment site, attP, was characterized using plasmid constructs, harbouring the integration functions, and serving as an integration probe in both P. aeruginosa and Escherichia coli. The attP plasmids p1000/p400 in the presence of the int plasmid pIBH and attP-int plasmids pINT/pINTS can be stably integrated into the P. aeruginosa chromosome. Successful recombination between the attP plasmid p1000 and the attB plasmid p5.1, in the presence of the int plasmid pIBH in E. coli HB101 showed that the int gene is active in trans in E. coli. The int gene product was detected as a 43 kDa protein in E. coli maxicells harbouring pINT. Proposed integration arm regions downstream of attP are not necessary for the integration process. pINT and phage phi CTX could be integrated together into P. aeruginosa chromosomal DNA, yielding double integrates.
分析了携带成孔细胞毒素基因的噬菌体phi CTX基因组在铜绿假单胞菌染色体中的位点特异性整合。位于附着位点attP上游紧邻位置的1167 bp整合酶基因int,使用携带整合功能并在铜绿假单胞菌和大肠杆菌中作为整合探针的质粒构建体进行了表征。attP质粒p1000/p400在int质粒pIBH和attP-int质粒pINT/pINTS存在的情况下可稳定整合到铜绿假单胞菌染色体中。在大肠杆菌HB101中,attP质粒p1000与attB质粒p5.1在int质粒pIBH存在的情况下成功重组,表明int基因在大肠杆菌中可反式发挥作用。在携带pINT的大肠杆菌最大细胞中,int基因产物被检测为一种43 kDa的蛋白质。attP下游提议的整合臂区域对于整合过程并非必需。pINT和噬菌体phi CTX可一起整合到铜绿假单胞菌染色体DNA中,产生双整合体。