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GacA 直接调控丁香假单胞菌 pv. 番茄 11528 中几个毒力基因的表达。

GacA directly regulates expression of several virulence genes in Pseudomonas syringae pv. tabaci 11528.

机构信息

Department of Microbiology, College of Natural Science, Pusan National University, Busan 609-735, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2012 Jan 13;417(2):665-72. doi: 10.1016/j.bbrc.2011.11.124. Epub 2011 Dec 7.

Abstract

A two-component system comprising GacS and GacA affects a large number of traits in many Gram-negative bacteria. However, the signals to which GacS responds, the regulation mechanism for GacA expression, and the genes GacA controls are not yet clear. In this study, several phenotypic tests and tobacco-leaf pathogenicity assays were conducted using a gacA deletion mutant strain (BL473) of Pseudomonas syringae pv. tabaci 11528. To determine the regulation mechanism for gacA gene expression and to identify GacA-regulated genes, we conducted quantitative RT-PCR and electrophoretic mobility shift assay (EMSA) experiments. The results indicated that virulence traits related to the pathogenesis of P. syringae pv. tabaci 11528 are regulated coordinately by GacA and iron availability. They also revealed that several systems coordinately regulate gacA gene expression in response to iron concentration and bacterial cell density and that GacA and iron together control the expression of several virulence genes. EMSA results provided genetic and molecular evidence for direct control of virulence genes by GacA.

摘要

由 GacS 和 GacA 组成的双组分系统影响许多革兰氏阴性细菌的许多性状。然而,GacS 响应的信号、GacA 表达的调节机制以及 GacA 控制的基因尚不清楚。在这项研究中,我们使用丁香假单胞菌 pv.番茄溃疡病 11528 的 gacA 缺失突变株 (BL473) 进行了几项表型测试和烟草叶片致病性测定。为了确定 gacA 基因表达的调节机制并鉴定 GacA 调控的基因,我们进行了定量 RT-PCR 和电泳迁移率变动分析 (EMSA) 实验。结果表明,丁香假单胞菌 pv.番茄溃疡病 11528 的发病机制相关的毒力性状受 GacA 和铁可用性的协调调节。结果还表明,几种系统通过响应铁浓度和细菌细胞密度协同调节 gacA 基因表达,并且 GacA 和铁共同控制几种毒力基因的表达。EMSA 结果为 GacA 对毒力基因的直接控制提供了遗传和分子证据。

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