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来自广宿主范围质粒RK2的最小质粒稳定系统的定义。

Definition of a minimal plasmid stabilization system from the broad-host-range plasmid RK2.

作者信息

Roberts R C, Helinski D R

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093-0634.

出版信息

J Bacteriol. 1992 Dec;174(24):8119-32. doi: 10.1128/jb.174.24.8119-8132.1992.

Abstract

The stable inheritance of the broad-host-range plasmid RK2 is due at least in part to functions within a region located at coordinates 32.8 to 35.9 kb, termed the RK2 par locus. This locus encodes four previously identified genes in two operons (parCBA and parD; M. Gerlitz, O. Hrabak, and H. Schwab, J. Bacteriol. 172:6194-6203, 1990, and R. C. Roberts, R. Burioni, and D. R. Helinski, J. Bacteriol. 172:6204-6216, 1990). The parCBA operon is functional in resolving plasmid multimers to monomers. Analysis of the plasmid stabilization capacity of deletions within this region, however, indicates that this multimer resolution operon is required for stabilization only in certain Escherichia coli strains and under specific growth conditions. The deletion analysis further allowed a redefinition of the minimal functional region as 790 bp in length, consisting of the parD gene (243 bp) and its promoter as well as sequences downstream of parD. This minimal region stabilizes an RK2-derived minireplicon in several different gram-negative bacteria and, at least in E. coli, in a vector-independent manner. By insertional mutagenesis, both the parD gene and downstream (3') regions were found to be required for plasmid stabilization. The downstream DNA sequence contained an open reading frame which was subsequently shown by transcriptional and translational fusions to encode a protein with a predicted size of 11,698 Da, designated ParE. Since the parDE operon requires the presence of the parCBA operon for efficient stabilization under certain growth conditions, the potential role of multimer resolution in plasmid stabilization was tested by substituting the ColE1 cer site for the parCBA operon. While the cer site did function to resolve plasmid multimers, it was not sufficient to restore stabilization activity to the parDE operon under growth conditions that require the parCBA operon for plasmid stability. This suggests that plasmid stabilization by the RK2 par locus relies on a complex mechanism, representing a multifaceted stabilization system of which multimer resolution is a conditionally dispensable component, and that the function(s) encoded by the parDE operon is essential.

摘要

广宿主质粒RK2的稳定遗传至少部分归因于位于坐标32.8至35.9 kb区域内的功能,该区域称为RK2 par位点。该位点在两个操纵子(parCBA和parD;M. Gerlitz、O. Hrabak和H. Schwab,《细菌学杂志》172:6194 - 6203,1990年,以及R. C. Roberts、R. Burioni和D. R. Helinski,《细菌学杂志》172:6204 - 6216,1990年)中编码四个先前已鉴定的基因。parCBA操纵子在将质粒多聚体解析为单体方面发挥作用。然而,对该区域内缺失的质粒稳定能力分析表明,这种多聚体解析操纵子仅在某些大肠杆菌菌株和特定生长条件下对于稳定化是必需的。缺失分析进一步允许将最小功能区域重新定义为长度790 bp,由parD基因(243 bp)及其启动子以及parD下游的序列组成。这个最小区域在几种不同的革兰氏阴性细菌中稳定一个源自RK2的微型复制子,并且至少在大肠杆菌中,以一种不依赖载体的方式起作用。通过插入诱变,发现parD基因和下游(3')区域对于质粒稳定化都是必需的。下游DNA序列包含一个开放阅读框,随后通过转录和翻译融合表明其编码一个预测大小为11,698 Da的蛋白质,命名为ParE。由于在某些生长条件下parDE操纵子需要parCBA操纵子的存在才能实现有效稳定化,因此通过用ColE1 cer位点替代parCBA操纵子来测试多聚体解析在质粒稳定化中的潜在作用。虽然cer位点确实起到了解析质粒多聚体的作用,但在需要parCBA操纵子来实现质粒稳定的生长条件下,它不足以恢复parDE操纵子的稳定活性。这表明RK2 par位点介导的质粒稳定化依赖于一种复杂机制,代表了一个多方面的稳定系统,其中多聚体解析是一个条件性可缺失的组成部分,并且parDE操纵子编码的功能是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4e8/207551/5bf252c48f46/jbacter00090-0257-a.jpg

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