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酵母拓扑异构酶I的纯化与特性分析

Purification and characterization of yeast topoisomerase I.

作者信息

Badaracco G, Plevani P, Ruyechan W T, Chang L M

出版信息

J Biol Chem. 1983 Feb 10;258(3):2022-6.

PMID:6296118
Abstract

Yeast topoisomerase I (Mr = 76,000) has been purified to 80% homogeneity using a combination of ion exchange, gel filtration, and DNA-cellulose chromatography. The enzyme was characterized with respect to its ability to relax supercoiled DNA and to catenate nicked circular DNA. Yeast topoisomerase I will remove both positive and negative turns in DNA supercoils in the absence of ATP and magnesium ion. The products of the catenating activity of the enzyme were examined on agarose gels and in the electron microscope. These analyses indicate that yeast topoisomerase I will generate large catenated DNA networks which appear to rearrange to multimeric linear structures upon long incubation time.

摘要

酵母拓扑异构酶I(分子量=76,000)通过离子交换、凝胶过滤和DNA纤维素色谱法相结合的方法纯化至80%的纯度。对该酶在松弛超螺旋DNA和连环化带切口环状DNA方面的能力进行了表征。酵母拓扑异构酶I在没有ATP和镁离子的情况下能够去除DNA超螺旋中的正、负超螺旋圈。在琼脂糖凝胶和电子显微镜下对该酶的连环化活性产物进行了检测。这些分析表明,酵母拓扑异构酶I会产生大型连环化DNA网络,在长时间孵育后似乎会重排为多聚体线性结构。

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