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在整合宿主因子(IHF)突变体中,来自oriC的染色体复制的利福平抗性起始。

Rifampicin-resistant initiation of chromosome replication from oriC in ihf mutants.

作者信息

Von Freiesleben U, Rasmussen K V, Atlung T, Hansen F G

机构信息

Department of Microbiology, Technical University of Denmark, Building 301, DK-2800 Lyngby, Denmark.

出版信息

Mol Microbiol. 2000 Sep;37(5):1087-93. doi: 10.1046/j.1365-2958.2000.02060.x.

Abstract

IHF (integration host factor) mutants exhibit asynchronous initiation of chromosome replication from oriC as determined from flow cytometric analysis of cultures where RNA synthesis was inhibited with rifampicin. However, the run-out kinetics of chromosome replication in ihf mutants shows that they continue to produce oriCs for some time in the absence of RNA synthesis resulting in a twofold increase in the oriC per mass ratio. An ihf dnaA double mutant did not exhibit this continued increase of the oriC per mass ratio. This indicates that ihf mutants can initiate replication from oriC in a rifampicin-resistant initiation mode but requires fully functional DnaA protein. The origin per mass ratio, determined by a quantitative Southern blotting technique, showed that the ihf mutants had an origin per mass ratio that was 60% of the wild type although it had a normal DnaA protein concentration. This shows that the initiation mass was substantially higher in the ihf mutants. The oriC per terminus ratio, which was also determined by Southern blotting, was very low in the ihf mutant, although it grew with the same doubling times as the wild-type strain. This indicates that cells lacking IHF replicate their chromosome(s) very fast.

摘要

整合宿主因子(IHF)突变体表现出从oriC开始的染色体复制起始异步,这是通过对用利福平抑制RNA合成的培养物进行流式细胞术分析确定的。然而,ihf突变体中染色体复制的延伸动力学表明,在没有RNA合成的情况下,它们在一段时间内继续产生oriC,导致oriC与质量比增加两倍。ihf dnaA双突变体并未表现出oriC与质量比的这种持续增加。这表明ihf突变体可以以利福平抗性起始模式从oriC起始复制,但需要功能完全正常的DnaA蛋白。通过定量Southern印迹技术测定的oriC与质量比表明,尽管ihf突变体具有正常的DnaA蛋白浓度,但其oriC与质量比仅为野生型的60%。这表明ihf突变体中的起始质量显著更高。同样通过Southern印迹测定的oriC与染色体末端比在ihf突变体中非常低,尽管其生长倍增时间与野生型菌株相同。这表明缺乏IHF的细胞非常快速地复制其染色体。

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