Dubnau E, Maas W K
J Bacteriol. 1968 Feb;95(2):531-9. doi: 10.1128/jb.95.2.531-539.1968.
Hfr strains of Escherichia coli K-12 were found capable of accepting a F'lac episome during mating, with a frequency approximating that of F(-) strains. However, the F'lac episome was unable to replicate in the Hfr cells, and was diluted out during the growth of the culture. The lac(+) gene of the episome can be "rescued" by recombination into the host chromosome, as shown by the appearance of variegated recombinant colonies on a lactose-fermentation indicator medium. In recA Hfr strains, however, no lac(+) offspring were obtained in crosses with F'lac donors. The induced synthesis of beta-galactosidase in F'lac(+) x Hfr zygotes was studied. Rates of enzyme synthesis were approximately constant with respect to time as expected from unilinear inheritance of the F'lac episome. However, the rate of synthesis eventually increased, presumably due to integration of the lac(+) gene in some of the zygotes. In F'lac(+) x recA Hfr zygotes the rate of beta-galactosidase synthesis remained constant with respect to time, as expected.
发现大肠杆菌K-12的高频重组(Hfr)菌株在交配过程中能够接受F'lac附加体,其频率与F(-)菌株相近。然而,F'lac附加体在Hfr细胞中无法复制,并在培养物生长过程中被稀释掉。附加体的lac(+)基因可通过重组进入宿主染色体而“获救”,这在乳糖发酵指示培养基上出现的斑驳重组菌落中得到了证明。然而,在recA Hfr菌株中,与F'lac供体杂交时未获得lac(+)后代。对F'lac(+)×Hfr合子中β-半乳糖苷酶的诱导合成进行了研究。正如从F'lac附加体的单线性遗传所预期的那样,酶合成速率随时间大致保持恒定。然而,合成速率最终增加,推测是由于一些合子中lac(+)基因的整合。在F'lac(+)×recA Hfr合子中,β-半乳糖苷酶的合成速率如预期的那样随时间保持恒定。