Dithiothreitol pretreatment and inducible repair in UV-irradiated Escherichia coli K12 cells.

H G Claycamp
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引用次数: 10

Abstract

The UV radiation survival of several Escherichia coli K12 strains was measured after pretreatment of the cells with dithiothreitol (DTT). In DNA repair-competent cells (AB1157), UV survival was enhanced (ER = 1.2) after pretreating cells for 1.0 h using 10 mmol dm-3 DTT and then incubating the cells for 1.5 h in buffer before UV irradiation. Similar experiments using the excision repair mutant, AB1886uvrA6, or the recombination repair and SOS-deficient mutant, AB2462recA, strains did not show enhanced UV survival. None of the E. coli strains tested were protected against UV killing by simultaneous treatment with DTT (10 mmol dm-3). These results, and the fact that incubation in chloramphenicol removed the wild-type response in DTT-pretreated, UV-irradiated cells, suggest that the observed UV radioprotection was a result of inducible enzymatic repair processes such as recA-dependent repair. The proposed stimulus for inducible repair in these cells is DNA damage caused by intracellular hydroxyl radicals arising from thiol oxidation. The involvement of oxygen radicals in the induction pathway is supported by results that showed superoxide dismutase and catalase could inhibit a portion (one-third) of the inducible repair.

二硫苏糖醇预处理及紫外辐照大肠杆菌K12细胞的诱导修复。
用二硫苏糖醇(DTT)预处理多株大肠杆菌K12,测定其紫外辐射存活率。在DNA修复能力细胞(AB1157)中,用10 mmol dm-3 DTT预处理细胞1.0 h,然后在紫外线照射前在缓冲液中孵育1.5 h,增强了细胞的紫外线存活率(ER = 1.2)。在类似的实验中,使用切除修复突变体AB1886uvrA6或重组修复和sos缺陷突变体AB2462recA,菌株的紫外线存活率没有提高。DTT (10 mmol dm-3)同时处理后,所有大肠杆菌菌株均未被紫外线杀灭。这些结果,以及在氯霉素中孵育去除dtt预处理、紫外线照射细胞的野生型反应的事实表明,观察到的紫外线辐射保护是诱导酶修复过程(如reca依赖性修复)的结果。在这些细胞中诱导修复的刺激是由硫醇氧化引起的细胞内羟基自由基引起的DNA损伤。结果表明,超氧化物歧化酶和过氧化氢酶可以抑制部分(三分之一)的诱导修复,这支持了氧自由基参与诱导途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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