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大肠杆菌K-12紫外线照射后脱氧核糖核酸双链断裂的酶促产生

Enzymatic production of deoxyribonucleic acid double-strand breaks after ultraviolet irradiation of Escherichia coli K-12.

作者信息

Bonura T, Smith K C

出版信息

J Bacteriol. 1975 Feb;121(2):511-7. doi: 10.1128/jb.121.2.511-517.1975.

Abstract

We have observed the enzymatic production of deoxyribonucleic acid (DNA) doublestrand breaks in Escherichia coli K12 after ultraviolet irradiation. Doublestrand breaks appeared in wild-type, polA1, recB21, recA, and exrA strains after incubation in minimal medium. THE UVRA6 strain showed no evidence of double-strand breakage under the same conditions. Our data suggest that uvr+ cells, which are proficient in the incision step of excision repair, accumulate double-strand breaks in their DNA as a result of the excision repair process, i.e., arising from closely matched incisions, excision gaps, or incisions and gaps on opposite strands of the DNA twin helix. Furthermore, strains deficient in excision repair subsequent to the incision step (i.e., polA, rec, exrA) showed more double-strand breaks than the wild type strain. The results raise the possibility that a significant fraction of the lethal events in ultraviolet-irradiated, repair-proficient (uvr+) cell may be enzymatically-induced DNA double-strand breaks.

摘要

我们观察到,紫外线照射后,大肠杆菌K12中会发生酶促产生脱氧核糖核酸(DNA)双链断裂的现象。在基本培养基中培养后,野生型、polA1、recB21、recA和exrA菌株中均出现了双链断裂。在相同条件下,uvrA6菌株未显示出双链断裂的迹象。我们的数据表明,在切除修复的切口步骤中功能完备的uvr+细胞,其DNA会由于切除修复过程而积累双链断裂,也就是说,这些双链断裂源于DNA双螺旋相对链上紧密匹配的切口、切除缺口或切口与缺口。此外,在切口步骤之后切除修复功能缺陷的菌株(即polA、rec、exrA)比野生型菌株表现出更多的双链断裂。这些结果增加了一种可能性,即在紫外线照射且修复功能完备(uvr+)的细胞中,相当一部分致死事件可能是由酶诱导的DNA双链断裂导致的。

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