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一种针对作用于脱嘌呤位点的核酸内切酶的新型检测方法及其在测量酿酒酵母修复缺陷突变体中AP核酸内切酶活性方面的应用。

A novel assay for endonucleases acting at apurinic sites and its use in measuring AP endonuclease activity in repair-deficient mutants of Saccharomyces cerevisiae.

作者信息

Futcher A B, Morgan A R

出版信息

Can J Biochem. 1979 Jun;57(6):932-7. doi: 10.1139/o79-113.

Abstract

A quick and convenient assay for depurination and AP endonuclease activities has been developed. (The term 'AP endonuclease' refers to a nuclease that acts on apurinic and probably apyrimidinic sites on DNA.) It is based on the observation that different topological forms of DNA, such as open circular DNA and covalently closed circular DNA, bind different amounts of the fluorescent intercalator ethidium bromide, and can therefore be distinguished by their fluorescence. This assay has been used to measure AP endonuclease activity in 22 repair-deficient mutants of Saccharomyces cerevisiae. All 22 had normal or nearly normal AP endonuclease activity. The AP endonuclease activity was partially characterized.

摘要

已开发出一种用于检测脱嘌呤和AP核酸内切酶活性的快速便捷方法。(术语“AP核酸内切酶”指作用于DNA上无嘌呤位点以及可能的无嘧啶位点的核酸酶。)该方法基于这样的观察结果:不同拓扑形式的DNA,如开环DNA和共价闭合环状DNA,结合不同量的荧光嵌入剂溴化乙锭,因此可以通过它们的荧光来区分。此方法已用于测量酿酒酵母22个修复缺陷型突变体中的AP核酸内切酶活性。所有22个突变体都具有正常或接近正常的AP核酸内切酶活性。对AP核酸内切酶活性进行了部分表征。

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