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弧菌科的极鞭毛运动性。

Polar flagellar motility of the Vibrionaceae.

作者信息

McCarter L L

机构信息

Department of Microbiology, The University of Iowa, Iowa City, IA 52242, USA.

出版信息

Microbiol Mol Biol Rev. 2001 Sep;65(3):445-62, table of contents. doi: 10.1128/MMBR.65.3.445-462.2001.

Abstract

Polar flagella of Vibrio species can rotate at speeds as high as 100,000 rpm and effectively propel the bacteria in liquid as fast as 60 microm/s. The sodium motive force powers rotation of the filament, which acts as a propeller. The filament is complex, composed of multiple subunits, and sheathed by an extension of the cell outer membrane. The regulatory circuitry controlling expression of the polar flagellar genes of members of the Vibrionaceae is different from the peritrichous system of enteric bacteria or the polar system of Caulobacter crescentus. The scheme of gene control is also pertinent to other members of the gamma purple bacteria, in particular to Pseudomonas species. This review uses the framework of the polar flagellar system of Vibrio parahaemolyticus to provide a synthesis of what is known about polar motility systems of the Vibrionaceae. In addition to its propulsive role, the single polar flagellum of V. parahaemolyticus is believed to act as a tactile sensor controlling surface-induced gene expression. Under conditions that impede rotation of the polar flagellum, an alternate, lateral flagellar motility system is induced that enables movement through viscous environments and over surfaces. Although the dual flagellar systems possess no shared structural components and although distinct type III secretion systems direct the simultaneous placement and assembly of polar and lateral organelles, movement is coordinated by shared chemotaxis machinery.

摘要

弧菌属的极鞭毛能够以高达100,000转/分钟的速度旋转,并能在液体中以高达60微米/秒的速度有效地推动细菌前进。钠动力为作为推进器的鞭毛丝的旋转提供动力。鞭毛丝结构复杂,由多个亚基组成,并被细胞外膜的延伸部分所包裹。控制弧菌科成员极鞭毛基因表达的调控电路不同于肠道细菌的周生鞭毛系统或新月柄杆菌的极鞭毛系统。基因控制模式也适用于γ-紫色细菌的其他成员,特别是假单胞菌属。本综述以副溶血性弧菌的极鞭毛系统为框架,综合介绍了弧菌科极运动系统的相关知识。除了其推进作用外,副溶血性弧菌的单根极鞭毛还被认为充当触觉传感器,控制表面诱导的基因表达。在阻碍极鞭毛旋转的条件下,会诱导出另一种侧向鞭毛运动系统,使细菌能够在粘性环境中移动并在表面上移动。尽管这两种鞭毛系统没有共同的结构成分,尽管不同的III型分泌系统指导极鞭毛和侧向细胞器的同时定位和组装,但运动是由共同的趋化机制协调的。

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