Cress D E, Kline B C
J Bacteriol. 1976 Feb;125(2):635-42. doi: 10.1128/jb.125.2.635-642.1976.
We have isolated chromosomal mutants of an Escherchia coli K-12 strain that maintain higher levels of an F' plasmid. The mutants are designated as plasmid copy number (pcn) mutants. They were detected by selecting for increased lactose fermentation in bacteria deleted for the lac operon but harboring an F'lacI,P pro+ plasmid. When examined for the amount of F' plasmid deoxyribonucleic acid (DNA) by the dye-CsCl isopycnic technique, the mutants show two to seven times as much covalently closed, circular (CCC) DNA as does the parental strain. The increased plasmid level in one mutant strain (pcn-24) was confirmed by DNA-DNA hybridization; however, this latter technique indicated about a twofold lower increase when compared with the increase measured for pcn-24 by the dye-CsCl technique. In mutant pcn-24 the increased amount of F' DNA reflects a proportional increase in monomeric-size plasmid molecules because oligomeric forms are not found. Also, in mutant pcn-24 the extra CCC plasmid copies do not seem to be randomly distributed throughout the cell's cytoplasm but appear complexed in situ with their host's folded chromosome. In all pcn mutants examined to date, the classical sex factor F is maintained at normal levels, whereas the viral plasmid Pl CM is maintained at two to three times the normal level. In all 17 pcn mutants isolated, the pcn mutation maps on the chromosome and not on the plasmid. Finally, the absolute amount of CCC F' DNA detectable in lysates of the six different pcn mutants examined decreased 50 to 90% upon incubation of the lysate at 37 C. In contrast, no loss of CCC DNA occurs when lysates of the parental F' strain are incubated at 37 C.
我们分离出了大肠杆菌K-12菌株的染色体突变体,这些突变体能维持更高水平的F'质粒。这些突变体被命名为质粒拷贝数(pcn)突变体。它们是通过在缺失乳糖操纵子但携带F'lacI、P pro+质粒的细菌中选择增强的乳糖发酵来检测的。当通过染料-CsCl等密度技术检测F'质粒脱氧核糖核酸(DNA)的量时,突变体显示出的共价闭合环状(CCC)DNA是亲本菌株的两到七倍。通过DNA-DNA杂交证实了一个突变菌株(pcn-24)中质粒水平的升高;然而,与通过染料-CsCl技术测量的pcn-24的增加相比,后一种技术显示的增加约低两倍。在突变体pcn-24中,F' DNA量的增加反映了单体大小质粒分子的成比例增加,因为未发现寡聚形式。此外,在突变体pcn-24中,额外的CCC质粒拷贝似乎不是随机分布在整个细胞的细胞质中,而是在原位与宿主折叠的染色体形成复合物。在迄今为止检测的所有pcn突变体中,经典性因子F维持在正常水平,而病毒质粒Pl CM维持在正常水平的两到三倍。在分离出的所有17个pcn突变体中,pcn突变位于染色体上而非质粒上。最后,在所检测的六个不同pcn突变体的裂解物中可检测到的CCC F' DNA的绝对量在裂解物于37℃孵育后减少了50%至90%。相比之下,亲本F'菌株的裂解物在37℃孵育时未发生CCC DNA的损失。