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尿嘧啶-DNA糖基化酶在大肠杆菌K-12中引发5-溴脱氧尿苷光致敏作用。

Uracil-DNA glycosylase causes 5-bromodeoxyuridine photosensitization in Escherichia coli K-12.

作者信息

Yamamoto Y, Fujiwara Y

机构信息

Department of Radiation Biophysics, Kobe University School of Medicine, Japan.

出版信息

J Bacteriol. 1990 Sep;172(9):5278-85. doi: 10.1128/jb.172.9.5278-5285.1990.

Abstract

An Escherichia coli uracil-DNA glycosylase-defective mutant (ung-1 thyA) was more resistant than its wild-type counterpart (ung+ thyA) to the killing effect of UV light when cultured in medium containing 5-bromouracil or 5-bromo-2'-deoxyuridine (BrdUrd). The phenotype of resistance to BrdUrd photosensitization and the uracil-DNA glycosylase deficiency appeared to be 100% cotransduced by P1 phage. During growth with BrdUrd, both strains exhibited similar growth rates and 5-bromouracil incorporation into DNA. The resistant phenotype of the ung-1 mutant was observed primarily during the stationary phase. In cells carrying 5-bromouracil-substituted DNA, mutations causing resistance to rifampin and valine were induced by UV irradiation at a higher frequency in the wild type than in the ung-1 mutant. This Ung-dependent UV mutagenesis required UmuC function. These results suggest that the action of the uracil-DNA glycosylase on UV-irradiated 5-bromouracil-substituted DNA produces lethal and mutagenic lesions. The BrdUrd photosensitization-resistant phenotype allowed us to develop a new, efficient method for enriching and screening ung mutants.

摘要

当在含有5-溴尿嘧啶或5-溴-2'-脱氧尿苷(BrdUrd)的培养基中培养时,大肠杆菌尿嘧啶-DNA糖基化酶缺陷型突变体(ung-1 thyA)比其野生型对应物(ung+ thyA)对紫外线的杀伤作用更具抗性。对BrdUrd光致敏的抗性表型和尿嘧啶-DNA糖基化酶缺陷似乎通过P1噬菌体100%共转导。在含有BrdUrd的培养基中生长期间,两种菌株表现出相似的生长速率以及5-溴尿嘧啶掺入DNA的情况。ung-1突变体的抗性表型主要在稳定期观察到。在携带5-溴尿嘧啶取代DNA的细胞中,紫外线照射诱导对利福平和缬氨酸抗性的突变,野生型中的频率高于ung-1突变体。这种依赖Ung的紫外线诱变需要UmuC功能。这些结果表明尿嘧啶-DNA糖基化酶对紫外线照射的5-溴尿嘧啶取代DNA的作用产生致死性和诱变性损伤。BrdUrd光致敏抗性表型使我们能够开发一种新的、高效的方法来富集和筛选ung突变体。

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