Monk M, Kinross J
J Bacteriol. 1972 Mar;109(3):971-8. doi: 10.1128/jb.109.3.971-978.1972.
We have isolated a strain of Escherichia coli K-12 carrying a mutation, polA12, that results in the synthesis of a temperature-sensitive deoxyribonucleic acid (DNA) polymerase I. The double mutants polA12 recA56 and polA12 recB21, constructed at 30 C, are inviable at 42 C. About 90% of the cells of both double mutants die after 2 hr of incubation at 42 C. Both double mutants filament at 42 C and show a dependence on high cell density for growth at 30 C. In polA12 recB21 cells at 42 C, DNA and protein synthesis gradually stop in parallel. In polA12 recA56 cells, DNA synthesis continues for at least 1 hr at 42 C, and there is extensive DNA degradation. The results suggest that the primary lesion in these double mutants is not in DNA replication per se.
我们分离出了一株携带polA12突变的大肠杆菌K - 12,该突变导致合成一种温度敏感型脱氧核糖核酸(DNA)聚合酶I。在30℃构建的双突变体polA12 recA56和polA12 recB21在42℃时无法存活。在42℃孵育2小时后,两种双突变体中约90%的细胞死亡。两种双突变体在42℃时都会形成丝状体,并且在30℃时生长依赖于高细胞密度。在42℃的polA12 recB21细胞中,DNA和蛋白质合成会同时逐渐停止。在42℃的polA12 recA56细胞中,DNA合成至少持续1小时,并且存在广泛的DNA降解。结果表明,这些双突变体中的主要损伤并非在于DNA复制本身。