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新型反应调节蛋白失活有利于费氏弧菌生物膜形成和宿主定植。

Inactivation of a novel response regulator is necessary for biofilm formation and host colonization by Vibrio fischeri.

机构信息

Department of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL, USA.

出版信息

Mol Microbiol. 2011 Oct;82(1):114-30. doi: 10.1111/j.1365-2958.2011.07800.x. Epub 2011 Aug 30.

Abstract

The marine bacterium Vibrio fischeri uses a biofilm to promote colonization of its eukaryotic host Euprymna scolopes. This biofilm depends on the symbiosis polysaccharide (syp) locus, which is transcriptionally regulated by the RscS-SypG two-component regulatory system. An additional response regulator (RR), SypE, exerts both positive and negative control over biofilm formation. SypE is a novel RR protein, with its three putative domains arranged in a unique configuration: a central phosphorylation receiver (REC) domain flanked by two effector domains with putative enzymatic activities (serine kinase and serine phosphatase). To determine how SypE regulates biofilm formation and host colonization, we generated a library of SypE domain mutants. Our results indicate that the N-terminus inhibits biofilm formation, while the C-terminus plays a positive role. The phosphorylation state of SypE appears to regulate these opposing activities, as disruption of the putative site of phosphorylation results in a protein that constitutively inhibits biofilm formation. Furthermore, SypE restricts host colonization: (i) sypE mutants with constitutive inhibitory activity fail to efficiently initiate host colonization and (ii) loss of sypE partially alleviates the colonization defect of an rscS mutant. We conclude that SypE must be inactivated to promote symbiotic colonization by V. fischeri.

摘要

海洋细菌 Vibrio fischeri 使用生物膜来促进其真核宿主 Euprymna scolopes 的定植。该生物膜依赖于共生多糖(syp)基因座,该基因座受 RscS-SypG 双组分调节系统转录调控。另一个响应调节剂(RR)SypE 对生物膜形成具有正、负双重调控作用。SypE 是一种新型 RR 蛋白,其三个假定结构域以独特的构型排列:中央磷酸化受体(REC)结构域两侧是具有假定酶活性的两个效应结构域(丝氨酸激酶和丝氨酸磷酸酶)。为了确定 SypE 如何调节生物膜形成和宿主定植,我们生成了 SypE 结构域突变体文库。我们的结果表明,N 端抑制生物膜形成,而 C 端发挥积极作用。SypE 的磷酸化状态似乎调节这些相反的活性,因为破坏假定的磷酸化位点会导致蛋白持续抑制生物膜形成。此外,SypE 限制宿主定植:(i)具有持续抑制活性的 sypE 突变体不能有效地启动宿主定植;(ii)sypE 的缺失部分缓解了 rscS 突变体的定植缺陷。我们得出结论,必须使 SypE 失活才能促进 V. fischeri 的共生定植。

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