Wilkins B M
J Bacteriol. 1975 Jun;122(3):899-904. doi: 10.1128/jb.122.3.899-904.1975.
Three I-like conjugative plasmids, ColIdrd1, R144drd3, and R64drd11, which are derepressed for functions involved in conjugation, were found to suppress at least partially the phenotype of temperature-sensitive dnaG mutants of Escherichia coli K-12, as judged from the kinetics of deoxyribonucleic acid synthesis at elevated temperature in newly formed and established plasmid-containing strains. In contrast, the corresponding wild-type plasmids and three F-like derepressed conjugative plasmids, F101, R100drd1, and R1drd16, all failed to suppress. Suppression is presumably caused by a different plasmid-determined function from that which promotes survival of ultraviolet-irradiated bacteria, because both the wild-type I-like plasmids and their drd mutants protected irradiated bacteria. One possible interpretation of these results is that the product of a gene carried by certain I-like plasmids can substitute for the bacterial dnaG gene product during ongoing deoxyribonucleic acid replication.
发现三种I类接合质粒ColIdrd1、R144drd3和R64drd11,其参与接合的功能处于去阻遏状态,从新形成的和已建立的含质粒菌株在高温下的脱氧核糖核酸合成动力学判断,它们至少部分抑制了大肠杆菌K - 12温度敏感型dnaG突变体的表型。相比之下,相应的野生型质粒和三种F类去阻遏接合质粒F101、R100drd1和R1drd16均未能产生抑制作用。抑制作用推测是由一种不同于促进紫外线照射细菌存活的质粒决定功能引起的,因为野生型I类质粒及其drd突变体都能保护受照射的细菌。这些结果的一种可能解释是,某些I类质粒携带的基因产物在正在进行的脱氧核糖核酸复制过程中可以替代细菌的dnaG基因产物。