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1
Enzymatic production of deoxyribonucleic acid double-strand breaks after ultraviolet irradiation of Escherichia coli K-12.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
J Bacteriol. 1975 Feb;121(2):511-7. doi: 10.1128/jb.121.2.511-517.1975.
2
Separate branches of the uvr gene-dependent excision repair process in ultraviolet-irradiated Escherichia coli K-12 cells; their dependence upon growth medium and the polA, recA, recB, and exrA genes.紫外线照射的大肠杆菌K-12细胞中uvr基因依赖性切除修复过程的不同分支;它们对生长培养基以及polA、recA、recB和exrA基因的依赖性。
J Bacteriol. 1974 Feb;117(2):717-25. doi: 10.1128/jb.117.2.717-725.1974.
3
Evidence for the control by exrA and polA genes of two branches of the uvr gene-dependent excision repair pathway in Escherichia coli K-12.关于大肠杆菌K-12中uvr基因依赖性切除修复途径的两个分支受exrA和polA基因调控的证据。
J Bacteriol. 1973 Oct;116(1):175-82. doi: 10.1128/jb.116.1.175-182.1973.
4
X-ray sensitivity and repair capacity of a polA1 exrA strain of Escherichia coli K-12.大肠杆菌K-12的polA1 exrA菌株的X射线敏感性和修复能力
J Bacteriol. 1973 Apr;114(1):121-7. doi: 10.1128/jb.114.1.121-127.1973.
5
Repair of radiation-induced damage in Escherichia coli. II. Effect of rec and uvr mutations on radiosensitivity, and repair of x-ray-induced single-strand breaks in deoxyribonucleic acid.大肠杆菌中辐射诱导损伤的修复。II. rec和uvr突变对辐射敏感性的影响,以及脱氧核糖核酸中X射线诱导的单链断裂的修复
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6
Excision repair characteristics of recB - res - and uvrC - strains of Escherichia coli.大肠杆菌recB - res - 和uvrC - 菌株的切除修复特性
J Bacteriol. 1972 Dec;112(3):1237-46. doi: 10.1128/jb.112.3.1237-1246.1972.
7
Repair of near-ultraviolet (365 nm)-induced strand breaks in Escherichia coli DNA. The role of the polA and recA gene products.大肠杆菌DNA中近紫外线(365纳米)诱导的链断裂的修复。polA和recA基因产物的作用。
Biophys J. 1986 Feb;49(2):485-91. doi: 10.1016/S0006-3495(86)83658-X.
8
Requirement for protein synthesis in rec-dependent repair of deoxyribonucleic acid in Escherichia coli after ultraviolet or X irradiation.紫外线或X射线照射后大肠杆菌中依赖rec的脱氧核糖核酸修复过程中蛋白质合成的需求
J Bacteriol. 1972 Aug;111(2):575-85. doi: 10.1128/jb.111.2.575-585.1972.
9
Influence of thymine starvation on the integrity of deoxyribonucleic acid in Escherichia coli.胸腺嘧啶饥饿对大肠杆菌中脱氧核糖核酸完整性的影响。
J Bacteriol. 1971 Mar;105(3):733-8. doi: 10.1128/jb.105.3.733-738.1971.
10
Genetic and kinetic evidence for different types of postreplication repair in Escherichia coli B.大肠杆菌B中不同类型复制后修复的遗传学和动力学证据。
J Bacteriol. 1975 Jul;123(1):154-61. doi: 10.1128/jb.123.1.154-161.1975.

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Substitutions of short heterologous DNA segments of intragenomic or extragenomic origins produce clustered genomic polymorphisms.基因组内或基因组外来源的短异源DNA片段的替换会产生成簇的基因组多态性。
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Is a fully wrapped SSB-DNA complex essential for Escherichia coli survival?完全包裹的单链结合蛋白 - 脱氧核糖核酸(SSB-DNA)复合物对大肠杆菌的生存至关重要吗?
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10
Cyanide enhances hydrogen peroxide toxicity by recruiting endogenous iron to trigger catastrophic chromosomal fragmentation.氰化物通过募集内源性铁来引发灾难性的染色体断裂,从而增强过氧化氢的毒性。
Mol Microbiol. 2015 Apr;96(2):349-67. doi: 10.1111/mmi.12938. Epub 2015 Feb 18.

本文引用的文献

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Linkage of polynucleotides through phosphodiester bonds by an enzyme from Escherichia coli.来自大肠杆菌的一种酶通过磷酸二酯键连接多核苷酸。
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Three loci in Escherichia coli K-12 that control the excision of pyrimidine dimers and certain other mutagen products from DNA.大肠杆菌K-12中控制从DNA切除嘧啶二聚体和某些其他诱变产物的三个基因座。
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Ultraviolet- and X-ray-induced responses of a deoxyribonucleic acid polymerase-deficient mutant of Escherichia coli.紫外线和X射线诱导的大肠杆菌脱氧核糖核酸聚合酶缺陷型突变体的反应
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Dark recovery processes in Escherichia coli irradiated with ultraviolet light. I. Effect of rec mutations on liquid holding recovery.紫外线照射大肠杆菌后的暗修复过程。I. rec突变对液体保持修复的影响
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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.

DOI:10.1128/jb.121.2.511-517.1975
PMID:1089633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC245960/
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。