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由大肠杆菌引发体促进的复制性DNA解旋酶的链交换

Strand switching of a replicative DNA helicase promoted by the E. coli primosome.

作者信息

Allen G C, Dixon N E, Kornberg A

机构信息

Department of Biochemistry Beckman Center, Stanford University School of Medicine, California 94305.

出版信息

Cell. 1993 Aug 27;74(4):713-22. doi: 10.1016/0092-8674(93)90518-u.

Abstract

The E. coli primosome assembles at an origin on a single-stranded DNA, like that of phi X174, to promote replication of that template. Upon conversion to the duplex form, the primosome can generate a rolling circle product from this template. Rolling circle synthesis implies the transfer of the DnaB helicase from its initial loading site on the viral strand to a displaced complementary strand. Isolated primosomes promote only unit-length synthesis; supplementation with PriC, DnaC, and DnaT is necessary to reconstitute rolling circle synthesis. Rolling circle replication is sensitive to salts, whereas primosome assembly and unit-length synthesis are not. Thus, the primosome promotes two distinct reactions: assembly for first-round synthesis and strand switching for rolling circle synthesis.

摘要

大肠杆菌引发体在单链DNA的一个原点处组装,就像噬菌体X174的那样,以促进该模板的复制。转化为双链形式后,引发体可以从该模板产生滚环产物。滚环合成意味着DnaB解旋酶从其在病毒链上的初始加载位点转移到一条被置换的互补链上。分离的引发体仅促进单位长度的合成;补充PriC、DnaC和DnaT对于重建滚环合成是必要的。滚环复制对盐敏感,而引发体组装和单位长度合成则不敏感。因此,引发体促进两种不同的反应:第一轮合成的组装和滚环合成的链切换。

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