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在大肠杆菌中,腐草霉素通过巯基介导的DNA断裂作用

Sulphydryl-mediated DNA breakage by phlemomycin in Escherichia coli.

作者信息

Sleigh M J, Grigg G W

出版信息

Mutat Res. 1977 Feb;42(2):181-90. doi: 10.1016/s0027-5107(77)80022-5.

Abstract

Sulphydryl-mediated DNA breakage, which is induced by the antibiotic phleomycin in vitro, has been found to contribute significantly to the DNA damage produced by phleomycin in Escherichia coli. The effect of pleomycin was inhibited in vivo, as in vitro, by chelating agents, sulphydryl blocking agents and antioxidants. An increase in the intracellular concentration of free sulphydryl resulted in an increased response to phleomycin, while mutants containing very low levels of free sulphydryl due to a defect in glutathione synthesis showed greatly reduced DNA breakage, particularly at low phleomycin concentrations. In spheroplasts of these gshA mutants, restoration of the response to phleomycin of dithiothreitol. Sulphydryl-mediated breakage appears to be the principal mechanism for DNA damage in E. coli at libly enzymic, operates at higher phleomycin concentrations.

摘要

巯基介导的DNA断裂由抗生素博来霉素在体外诱导产生,已发现其对博来霉素在大肠杆菌中造成的DNA损伤有显著作用。与体外情况一样,博来霉素的作用在体内受到螯合剂、巯基阻断剂和抗氧化剂的抑制。细胞内游离巯基浓度的增加导致对博来霉素的反应增强,而由于谷胱甘肽合成缺陷而含有极低水平游离巯基的突变体显示出DNA断裂大大减少,尤其是在低博来霉素浓度下。在这些gshA突变体的原生质球中,二硫苏糖醇恢复了对博来霉素的反应。巯基介导的断裂似乎是大肠杆菌中DNA损伤的主要机制,在低酶活性下,在较高博来霉素浓度下起作用。

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