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萘啶酸诱导大肠杆菌中的瞬时DNA松弛

Transient DNA relaxation in Escherichia coli induced by nalidixic acid.

作者信息

Ohtsuka Y, Mizushima T, Miki T, Sekimizu K

机构信息

Department of Microbiology, Faculty of Pharmaceutical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan.

出版信息

Biol Pharm Bull. 1997 May;20(5):467-70. doi: 10.1248/bpb.20.467.

Abstract

We report here the transient relaxation of plasmid DNA by inhibitors of DNA gyrase in Escherichia coli. Relaxation of plasmid DNA in the presence of nalidixic acid, an inhibitor of the A subunit of DNA gyrase, lasted less than 60 min. The effect of nalidixic acid was not observed in a nalA26 mutant, a strain resistant to nalidixic acid due to a mutation in the gyrA gene. Novobiocin, whose target is the B subunit of DNA gyrase, also caused transient DNA relaxation. Resupercoiling of relaxed DNA in the presence of nalidixic acid was inhibited by pretreatment of the cells with chloramphenicol. As mutations of both the rpoH and recA genes did not affect the resupercoiling reaction, this step seems to require protein synthesis that is independent of both heat shock and SOS responses.

摘要

我们在此报告了大肠杆菌中DNA回旋酶抑制剂对质粒DNA的瞬时松弛作用。在萘啶酸(一种DNA回旋酶A亚基的抑制剂)存在的情况下,质粒DNA的松弛持续时间不到60分钟。在nalA26突变体中未观察到萘啶酸的作用,该突变体是由于gyrA基因发生突变而对萘啶酸具有抗性的菌株。新生霉素的作用靶点是DNA回旋酶的B亚基,它也会引起DNA的瞬时松弛。用氯霉素预处理细胞可抑制在萘啶酸存在下松弛DNA的再超螺旋化。由于rpoH和recA基因的突变均不影响再超螺旋化反应,因此这一步骤似乎需要独立于热休克和SOS反应的蛋白质合成。

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