Pritchard J J, Rowbury R J
Z Allg Mikrobiol. 1980;20(2):129-40. doi: 10.1002/jobm.3630200208.
The replication of R124, and a copy mutant derivative of it, was measured with respect to dependence on the host DnaA, DnaB, DnaC, DnaE, DnaG, and PolA gene products. Both plasmids replicated under conditions where the DnaA gene product was inactivated or where the polymerising activity of the PolA gene product was reduced. In contrast, neither plasmid replicated to any appreciable extent, if the DnaB, DnaC, DnaE or DnaG gene products were inactivated. R124 integratively suppressed the lesion of the dnaA mutant but the copy mutant derivative had only a very weak suppressing effect. Neither plasmid suppressed the lesions of any of the other dna mutants.
针对R124及其一个复制突变体衍生物对宿主DnaA、DnaB、DnaC、DnaE、DnaG和PolA基因产物的依赖性,对其复制情况进行了测定。在DnaA基因产物失活或PolA基因产物的聚合活性降低的条件下,两种质粒均能复制。相比之下,如果DnaB、DnaC、DnaE或DnaG基因产物失活,两种质粒均不会有明显程度的复制。R124整合抑制了dnaA突变体的损伤,但复制突变体衍生物的抑制作用非常微弱。两种质粒均未抑制其他任何dna突变体的损伤。