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鉴定炭疽芽孢杆菌质粒pXO1上对其维持至关重要的三个不相邻区域。

Identification of three noncontiguous regions on Bacillus anthracis plasmid pXO1 that are important for its maintenance.

作者信息

Pomerantsev Andrei P, Chang Zanetta, Rappole Catherine, Leppla Stephen H

机构信息

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA

出版信息

J Bacteriol. 2014 Aug 15;196(16):2921-33. doi: 10.1128/JB.01747-14. Epub 2014 Jun 9.

Abstract

Bacillus anthracis pXO1 minireplicon (MR) plasmid consisting of open reading frames (ORFs) GBAA_pXO1_0020 to GBAA_pXO1_0023 is not stably maintained in B. anthracis, whereas the full-size parent pXO1 plasmid (having 181,677 bp and 217 ORFs) is extremely stable under the same growth conditions. Two genetic tools developed for DNA manipulation in B. anthracis (Cre-loxP and Flp-FRT systems) were used to identify pXO1 regions important for plasmid stability. We localized a large segment of pXO1 that enables stable plasmid maintenance during vegetative growth. Further genetic analysis identified three genes that are necessary for pXO1 maintenance: amsP (GBAA_pXO1_0069), minP (GBAA_pXO1_0082), and sojP (GBAA_pXO1_0084). Analysis of conserved domains in the corresponding proteins indicated that only AmsP (activator of maintenance system of pXO1) is predicted to bind DNA, due to its strong helix-turn-helix domain. Two conserved domains were found in the MinP protein (Min protein from pXO1): an N-terminal domain having some similarity to the B. anthracis septum site-determining protein MinD and a C-terminal domain that resembles a baculovirus single-stranded-DNA-binding protein. The SojP protein (Soj from pXO1) contains putative Walker box motifs and belongs to the ParA family of ATPases. No sequences encoding other components of type I plasmid partition systems, namely, cis-acting centromere parS and its binding ParB protein, were identified within the pXO1 genome. A model describing the role of the MinP protein in pXO1 distribution between daughter cells is proposed.

摘要

由开放阅读框(ORF)GBAA_pXO1_0020至GBAA_pXO1_0023组成的炭疽芽孢杆菌pXO1微型复制子(MR)质粒在炭疽芽孢杆菌中不能稳定维持,而全长亲本pXO1质粒(有181,677 bp和217个ORF)在相同生长条件下极其稳定。为在炭疽芽孢杆菌中进行DNA操作而开发的两种遗传工具(Cre-loxP和Flp-FRT系统)被用于鉴定对质粒稳定性重要的pXO1区域。我们定位了pXO1的一大段区域,该区域能在营养生长期间实现稳定的质粒维持。进一步的遗传分析确定了pXO1维持所必需的三个基因:amsP(GBAA_pXO1_0069)、minP(GBAA_pXO1_0082)和sojP(GBAA_pXO1_0084)。对相应蛋白质中保守结构域的分析表明,由于其强大的螺旋-转角-螺旋结构域,只有AmsP(pXO1维持系统激活剂)预计能结合DNA。在MinP蛋白(来自pXO1的Min蛋白)中发现了两个保守结构域:一个N端结构域与炭疽芽孢杆菌隔膜位点决定蛋白MinD有一些相似性,一个C端结构域类似于杆状病毒单链DNA结合蛋白。SojP蛋白(来自pXO1的Soj)含有假定的沃克盒基序,属于ATP酶的ParA家族。在pXO1基因组内未鉴定到编码I型质粒分配系统其他组分的序列,即顺式作用着丝粒parS及其结合蛋白ParB。提出了一个描述MinP蛋白在pXO1在子细胞间分配中作用的模型。

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