Schmitt C K, Molineux I J
Department of Microbiology, University of Texas, Austin 78712.
J Bacteriol. 1991 Feb;173(4):1536-43. doi: 10.1128/jb.173.4.1536-1543.1991.
Plasmids expressing bacteriophage T7 gene 1.2 or gene 10 DNA transform F plasmid-containing strains of Escherichia coli only at low efficiency, though they transform plasmid-free strains normally. The gene products T7 gp1.2 and T7 gp10 appear to be the toxic agents, and their effects are directed towards the product of the F pifA gene, PifA. T7 gp1.2 and gp10 are also the two targets of the pif exclusion system of F, and their synthesis normally triggers the abortive infection of T7 in pifA+ hosts. The properties of plasmids containing T7 gene 1.2 or 10 suggest that they can be used to study the molecular mechanisms of phage exclusion in model systems that avoid the pleiotropic dysfunctions associated with an abortive infection.
表达噬菌体T7基因1.2或基因10 DNA的质粒仅以低效率转化含F质粒的大肠杆菌菌株,尽管它们能正常转化无质粒的菌株。基因产物T7 gp1.2和T7 gp10似乎是毒性因子,其作用针对F pifA基因的产物PifA。T7 gp1.2和gp10也是F的pif排斥系统的两个靶点,它们的合成通常会引发pifA+宿主中T7的流产感染。含有T7基因1.2或10的质粒的特性表明,它们可用于在避免与流产感染相关的多效性功能障碍的模型系统中研究噬菌体排斥的分子机制。