Schilf W, Krishnapillai V
Plasmid. 1986 Jan;15(1):48-56. doi: 10.1016/0147-619x(86)90013-2.
Transposon Tn7 insertion mutations of the promiscuous IncP-1 plasmid R18 which affect its conjugational transmissibility from Pseudomonas aeruginosa to Escherichia coli C, a strain of E. coli K12, Salmonella typhimurium and P. maltophilia have been mapped physically. They map to coordinate 53.5 kb in the Tral region of the plasmid. An 800-bp fragment mapping between R18 coordinates 52.85 and 53.65 kb, which complemented the host range defect of the mutants when tested with E. coli C as recipient, has been identified. However, complementation occurred only when the 800-bp cloned fragment was provided in the E. coli C recipient but not when situated in the P. aeruginosa donor. It is concluded that a trans-acting gene product of R18 is required, in the transcipient, for conjugative DNA metabolism during, or immediately following, the conjugational transfer of this plasmid between certain donor and recipient hosts.
对具有广泛宿主范围的IncP-1质粒R18进行转座子Tn7插入突变,该突变影响其从铜绿假单胞菌向大肠杆菌C(一种大肠杆菌K12菌株)、鼠伤寒沙门氏菌和嗜麦芽窄食单胞菌的接合传递能力,已对这些突变进行了物理定位。它们定位于质粒Tral区域的53.5 kb处。已鉴定出一个800 bp的片段,其定位于R18的52.85至53.65 kb之间,当以大肠杆菌C作为受体进行测试时,该片段可弥补突变体的宿主范围缺陷。然而,只有当800 bp的克隆片段存在于大肠杆菌C受体中时才会发生互补,而存在于铜绿假单胞菌供体中时则不会。得出的结论是,在某些供体和受体宿主之间进行该质粒的接合转移期间或之后,转座子R18的反式作用基因产物在受体中对于接合DNA代谢是必需的。