Kato T
Mol Gen Genet. 1977 Nov 14;156(2):115-20. doi: 10.1007/BF00283483.
Postreplication repair and its inhibition by chloramphenicol and caffeine, as seen in alkaline sucrose gradients, were compared between a uv non-mutable strain uvrA- umuC- and normally mutable strains uvrA- recF- and uvrA- umu+rec+ of Escherichia coli K-12. The uvrA- umuC- strain performed postreplication repair as efficiently as the parental strain, while the repair in uvrA- recF- strain was dependent on UV dose. Both chloramphenicol and caffeine inhibited postreplication repair to an equal extent of about 25%, and 10%, respectively, in all three uvrA- strains of umuC36, recF- and umu+rec+. These observations suggest that postreplication repair is largely not responsible for UV mutagenesis.
在碱性蔗糖梯度中观察到的复制后修复及其被氯霉素和咖啡因抑制的情况,在大肠杆菌K-12的uv非突变菌株uvrA-umuC-与正常可突变菌株uvrA-recF-和uvrA-umu+rec+之间进行了比较。uvrA-umuC-菌株进行复制后修复的效率与亲本菌株一样高,而uvrA-recF-菌株中的修复则取决于紫外线剂量。在umuC36、recF-和umu+rec+的所有三个uvrA-菌株中,氯霉素和咖啡因分别将复制后修复同等程度地抑制了约25%和10%。这些观察结果表明,复制后修复在很大程度上与紫外线诱变无关。