Suppr超能文献

氨基酸饥饿型大肠杆菌菌株中质粒pBR322复制的调控

Regulation of replication of plasmid pBR322 in amino acid-starved Escherichia coli strains.

作者信息

Herman A, Wegrzyn A, Wegrzyn G

机构信息

Department of Molecular Biology, University of Gdańsk, Poland.

出版信息

Mol Gen Genet. 1994 May 25;243(4):374-8. doi: 10.1007/BF00280467.

Abstract

The stringent response causes inhibition of replication of plasmid pBR322 in amino acid-starved Escherichia coli cells whereas in relaxed mutants the replication of this plasmid proceeds for several hours. On the basis of density shift experiments and pulse-labelling experiments we showed that most of the pBR322 molecules begin replication during the relaxed response and the rate of plasmid DNA synthesis in unstarved and isoleucine-starved relA- bacteria is similar. We found that the Rom function plays a key role in the stringent control of plasmid pBR322 replication, as insertional inactivation of the rom gene causes amplification of pBR322rom- in both relA- and relA+ strains during amino acid starvation. Moreover, pUC19, which is a pBR322-derived plasmid lacking the rom gene, behaves like pBR322rom-, whereas introduction of the rom gene into the pUC19 replicon drives it into the pBR322 mode of replication in amino acid-starved bacteria. A model for the regulation of pBR322 plasmid DNA replication by Rom protein in amino acid-starved Escherichia coli strains is proposed.

摘要

严紧反应会抑制质粒pBR322在氨基酸饥饿的大肠杆菌细胞中的复制,而在松弛突变体中,该质粒的复制会持续数小时。基于密度转移实验和脉冲标记实验,我们表明大多数pBR322分子在松弛反应期间开始复制,并且在未饥饿和异亮氨酸饥饿的relA-细菌中质粒DNA合成的速率相似。我们发现Rom功能在质粒pBR322复制的严紧控制中起关键作用,因为在氨基酸饥饿期间,rom基因的插入失活会导致relA-和relA+菌株中pBR322rom-的扩增。此外,pUC19是一种缺乏rom基因的pBR322衍生质粒,其行为类似于pBR322rom-,而将rom基因引入pUC19复制子会使其在氨基酸饥饿的细菌中进入pBR322复制模式。本文提出了一种在氨基酸饥饿的大肠杆菌菌株中由Rom蛋白调控pBR322质粒DNA复制的模型。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验