Barth P T, Ellis K, Bechhofer D H, Figurski D H
Mol Gen Genet. 1984;197(2):236-43. doi: 10.1007/BF00330969.
Plasmid pRP761 is a derivative of the promiscuous plasmid RP4, which has a Tn76 insert 1.8 kb from its EcoRI site within the trfB region (Barth 1979). This mutation was pleiotropic, having three effects: the plasmid is unstably maintained in E. coli, it reduces the growth rate of its host and it has suffered a reduction in host-range. We show that pRP761 has reduced expression from both its korA and korB genes and that Tn76 has inserted between them. Fragment exchange experiments showed that this is the only mutant region in pRP761 and is therefore solely responsible for the pleiotropic effects. A spontaneous deletion derivative pRP761-6 has lost Tn76 and its adjacent kilA and korA genes: it has reacquired stability, does not inhibit host growth but is still reduced in its host-range. The provision of cloned korA+ in trans complements the first two phenotypic effects in pRP761 to a large extent, but neither korA+ alone nor korA+ with korB+ complements the host-range reduction in pRP761 or pRP761-6. A possible explanation for these results is that there is a site between korA and korB, affected by the Tn76 insert, that is essential to stable replication of these plasmids in some of their bacterial hosts.
质粒pRP761是可转移性质粒RP4的衍生物,在trfB区域内,其EcoRI位点下游1.8 kb处有一个Tn76插入片段(Barth,1979)。该突变具有多效性,有三种效应:该质粒在大肠杆菌中不能稳定维持,它降低了宿主的生长速率,并且其宿主范围缩小。我们发现pRP761的korA和korB基因的表达均降低,且Tn76插入在它们之间。片段交换实验表明,这是pRP761中唯一的突变区域,因此是多效性效应的唯一原因。一个自发缺失衍生物pRP761-6丢失了Tn76及其相邻的kilA和korA基因:它恢复了稳定性,不抑制宿主生长,但宿主范围仍然缩小。反式提供克隆的korA +在很大程度上弥补了pRP761中的前两种表型效应,但单独的korA +或korA +与korB +都不能弥补pRP761或pRP761-6中宿主范围的缩小。这些结果的一个可能解释是,在korA和korB之间有一个受Tn76插入影响的位点,该位点对于这些质粒在其某些细菌宿主中的稳定复制至关重要。