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通过F接合系统稳定来自斯氏泛菌的pSW100。

Stabilization of pSW100 from Pantoea stewartii by the F conjugation system.

作者信息

Lin Mei-Hui, Liu Shih-Tung

机构信息

Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 333, Taiwan.

出版信息

J Bacteriol. 2008 May;190(10):3681-9. doi: 10.1128/JB.00846-07. Epub 2008 Mar 14.

Abstract

Plasmid pSW100 is 1 of the 13 plasmids from Pantoea stewartii subsp. stewartii SW2 which has a replicon that resembles that of ColE1. This work uses a pSW100 derivative, pSW140K, to study how the pSW100 replicon is stably maintained in its hosts. Our results indicate that although pSW140K is stable in Escherichia coli HB101, the plasmid is rapidly lost in another E. coli strain, DH5alpha, indicating that the genetic background of an E. coli strain affects the stability of pSW140K. Mutagenesis of E. coli HB101 with EZ::TN revealed that mutations in traC, traF, traG, traN, and traV, which encode the components of the sex pilus assembly, reduce plasmid stability. Furthermore, this work identified that a 38-bp region located immediately upstream of the RNAII promoter is critical to the maintenance of plasmid stability in E. coli HB101. TraC binds to the region, and in addition, deleting the region destabilizes the plasmid. Furthermore, inserting this 38-bp fragment into a plasmid that contains the minimal replicon from pSW200 stabilizes the plasmid in E. coli HB101. Fluorescence in situ hybridization and immunofluorescence staining also revealed that derivatives of pSW100, pSW128A, and TraC are colocalized in cells, suggesting that pSW100 may use the sex pilus assembly as a partition apparatus to ensure the even distribution of the plasmid during cell division, which may thus maintain the plasmid's stability.

摘要

质粒pSW100是来自斯氏泛菌斯氏亚种SW2的13种质粒之一,其复制子与ColE1的复制子相似。本研究使用pSW100的衍生物pSW140K来研究pSW100复制子如何在其宿主中稳定维持。我们的结果表明,虽然pSW140K在大肠杆菌HB101中是稳定的,但该质粒在另一株大肠杆菌DH5α中迅速丢失,这表明大肠杆菌菌株的遗传背景会影响pSW140K的稳定性。用EZ::TN 对大肠杆菌HB101进行诱变,结果显示,编码性菌毛组装成分的traC、traF、traG、traN和traV发生突变会降低质粒稳定性。此外,本研究还确定,位于RNAII启动子上游紧邻的一个38bp区域对于在大肠杆菌HB101中维持质粒稳定性至关重要。TraC与该区域结合,此外,删除该区域会使质粒不稳定。此外,将这个38bp的片段插入到含有pSW200最小复制子的质粒中,可使该质粒在大肠杆菌HB101中稳定。荧光原位杂交和免疫荧光染色还显示,pSW100的衍生物pSW128A和TraC在细胞中是共定位的,这表明pSW100可能利用性菌毛组装作为一种分配装置,以确保质粒在细胞分裂过程中均匀分布,从而维持质粒的稳定性。

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