Herman A, Wegrzyn A, Wegrzyn G
Department of Molecular Biology, University of Gdańsk, Poland.
Mol Gen Genet. 1994 May 25;243(4):374-8. doi: 10.1007/BF00280467.
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.
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。