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甲苯处理的大肠杆菌中的两种切除修复模式。

Two modes of excision repair in toluene-treated Escherichia coli.

作者信息

Sharon R, Miller C, Ben-Ishai R

出版信息

J Bacteriol. 1975 Sep;123(3):1107-14. doi: 10.1128/jb.123.3.1107-1114.1975.

Abstract

In toluene-treated Escherichia coli incision breaks accumulate during post-irradiation incubation in the presence of adenosine 5'-triphosphate (ATP). It is shown that incised deoxyribonucleic acid (DNA) is converted to high-molecular-weight DNA during reincubation in the presence of the four deoxyribonucleoside triphosphates (dNTP's) and nicotinamide adenine dinucleotide (NAD). This restitution process is ATP independent and N-ethylmaleimide insensitive and takes place only in polA+ strains. It is defective in strains carrying a mutation in the 5' leads to 3' exonucleolytic activity associated with DNA polymerase I. Repair of accumulated incision breaks differs from repair in which all the steps of the excision repair process occur simultaneously or in rapid succession. The latter is observed if toluene-treated E. coli are incubated immediately after irradiation in the presence of the four dNTP's, NAD, and ATP. It is shown that under these conditions dimer excision occurs to a larger extent than during repair of accumulated incision breaks and that, except in strains defective in polynucleotide ligase, incision breaks do not accumulate. This consecutive mode of repair is detectable in polA+ strains and at low doses also in polA mutants.

摘要

在甲苯处理过的大肠杆菌中,在存在腺苷5'-三磷酸(ATP)的情况下进行辐照后孵育期间,切口断裂会累积。结果表明,在存在四种脱氧核苷三磷酸(dNTP)和烟酰胺腺嘌呤二核苷酸(NAD)的情况下重新孵育时,切口的脱氧核糖核酸(DNA)会转化为高分子量DNA。这种修复过程不依赖ATP且对N-乙基马来酰亚胺不敏感,并且仅在polA +菌株中发生。在携带与DNA聚合酶I相关的5'至3'核酸外切酶活性突变的菌株中,该修复过程存在缺陷。累积切口断裂的修复与切除修复过程的所有步骤同时或快速连续发生的修复不同。如果在存在四种dNTP、NAD和ATP的情况下,对甲苯处理过的大肠杆菌在辐照后立即进行孵育,就会观察到后者。结果表明,在这些条件下,二聚体切除的程度比累积切口断裂的修复过程中更大,并且除了在多核苷酸连接酶缺陷的菌株中,切口断裂不会累积。这种连续的修复模式在polA +菌株中可检测到,在低剂量时在polA突变体中也可检测到。

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The ATP dependence of the incision and resynthesis steps of excision repair.
Biochim Biophys Acta. 1976 Aug 18;442(2):162-73. doi: 10.1016/0005-2787(76)90487-1.

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