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双鞭毛系统使生物在不同环境下具备运动能力。

Dual flagellar systems enable motility under different circumstances.

作者信息

McCarter Linda L

机构信息

Department of Microbiology, The University of Iowa, Iowa City, Iowa 52246, USA.

出版信息

J Mol Microbiol Biotechnol. 2004;7(1-2):18-29. doi: 10.1159/000077866.

Abstract

Flagella are extremely effective organelles of locomotion used by a variety of bacteria and archaea. Some bacteria, including Aeromonas, Azospirillum, Rhodospirillum, and Vibrio species, possess dual flagellar systems that are suited for movement under different circumstances. Swimming in liquid is promoted by a single polar flagellum. Swarming over surfaces or in viscous environments is enabled by the production of numerous peritrichous, or lateral, flagella. The polar flagellum is produced continuously, while the lateral flagella are produced under conditions that disable polar flagellar function. Thus at times, two types of flagellar organelles are assembled simultaneously. This review focuses on the polar and lateral flagellar systems of Vibrio parahaemolyticus. Approximately 50 polar and 40 lateral flagellar genes have been identified encoding distinct structural, motor, export/assembly, and regulatory elements. The sodium motive force drives polar flagellar rotation, and the proton motive force powers lateral translocation. Polar genes are found exclusively on the large chromosome, and lateral genes reside entirely on the small chromosome of the organism. The timing of gene expression corresponds to the temporal demand for components during assembly of the organelle: RpoN and lateral- and polar-specific sigma(54)-dependent transcription factors control early/intermediate gene transcription; lateral- and polar-specific sigma(28) factors direct late flagellar gene expression. Although a different gene set encodes each flagellar system, the constituents of a central navigation system (i.e., chemotaxis signal transduction) are shared.

摘要

鞭毛是多种细菌和古菌所使用的极其有效的运动细胞器。一些细菌,包括气单胞菌属、固氮螺菌属、红螺菌属和弧菌属,拥有双鞭毛系统,适合在不同环境下运动。单个极鞭毛促进在液体中游泳。通过产生大量周生鞭毛或侧生鞭毛,可在表面或粘性环境中群游。极鞭毛持续产生,而侧生鞭毛在使极鞭毛功能丧失的条件下产生。因此,有时两种类型的鞭毛细胞器会同时组装。本综述聚焦于副溶血性弧菌的极鞭毛和侧生鞭毛系统。已鉴定出约50个极鞭毛基因和40个侧生鞭毛基因,它们编码不同的结构、运动、输出/组装和调控元件。钠动力驱动极鞭毛旋转,质子动力为侧向移位提供动力。极鞭毛基因仅存在于大染色体上,侧生鞭毛基因完全位于该生物体的小染色体上。基因表达的时间与细胞器组装过程中对组件的时间需求相对应:RpoN以及侧生和极生特异性的σ54依赖性转录因子控制早期/中期基因转录;侧生和极生特异性的σ28因子指导鞭毛晚期基因表达。尽管每个鞭毛系统由不同的基因集编码,但中央导航系统(即趋化信号转导)的组成部分是共享的。

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