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黄色黏球菌中社会运动性所需的胞外多糖生物合成基因。

Exopolysaccharide biosynthesis genes required for social motility in Myxococcus xanthus.

作者信息

Lu Ann, Cho Kyunyung, Black Wesley P, Duan Xue-Yan, Lux Renate, Yang Zhaomin, Kaplan Heidi B, Zusman David R, Shi Wenyuan

机构信息

University of California-Los Angeles, Molecular Biology Institute and School of Dentistry, Los Angeles, CA 90095, USA.

出版信息

Mol Microbiol. 2005 Jan;55(1):206-20. doi: 10.1111/j.1365-2958.2004.04369.x.

Abstract

Social (S)-motility in Myxococcus xanthus is a flagellum-independent gliding motility system that allows bacteria to move in groups on solid surfaces. S-motility has been shown to require type IV pili (TFP), exopolysaccharide (EPS; a component of fibrils) and lipopolysaccharide (LPS). Previously, information concerning EPS biogenesis in M. xanthus was lacking. In this study, we screened 5000 randomly mutagenized colonies for defects in S-motility and EPS and identified two genetic regions essential for EPS biogenesis: the EPS synthesis (eps) region and the EPS-associated (eas) region. Mutants with insertions in the eps and eas regions were defective in S-motility and fruiting body formation. These mutants failed to bind the dye calcofluor white, indicating that they lacked EPS; however, they retained normal TFP and LPS. Analysis of the eps locus showed several open reading frames (ORFs) that encode homologues to glycosyltransferases, glucanases and EPS transporters as well as regulatory proteins; the eas locus contains two ORFs: one exhibits homology to hypothetical proteins with a conserved domain of unknown function and the other displays no apparent homology to other proteins in the database. Further genetic mutagenesis analysis indicates that the whole eps region is involved in the biosynthesis of fibrils and fibril EPS. The operon at the proximal end of the eps region was analysed by generating in-frame deletion mutations. These mutants showed varying degrees of defects in the bacterium's ability to produce EPS or perform EPS-related functions, confirming the involvement of these genes in M. xanthus EPS biogenesis.

摘要

黄色黏球菌的社会(S)-运动性是一种不依赖鞭毛的滑行运动系统,它能使细菌在固体表面成群移动。已证明S-运动性需要IV型菌毛(TFP)、胞外多糖(EPS;纤丝的一种成分)和脂多糖(LPS)。此前,关于黄色黏球菌中EPS生物合成的信息尚缺。在本研究中,我们筛选了5000个随机诱变的菌落,以寻找S-运动性和EPS方面的缺陷,并确定了EPS生物合成所必需的两个遗传区域:EPS合成(eps)区域和EPS相关(eas)区域。在eps和eas区域有插入突变的突变体在S-运动性和子实体形成方面存在缺陷。这些突变体无法结合染料荧光增白剂,表明它们缺乏EPS;然而,它们保留了正常的TFP和LPS。对eps位点的分析显示了几个开放阅读框(ORF),它们编码与糖基转移酶、葡聚糖酶和EPS转运蛋白以及调节蛋白同源的蛋白;eas位点包含两个ORF:一个与具有未知功能保守结构域的假定蛋白具有同源性,另一个在数据库中与其他蛋白没有明显同源性。进一步的遗传诱变分析表明,整个eps区域参与纤丝和纤丝EPS的生物合成。通过产生框内缺失突变对eps区域近端的操纵子进行了分析。这些突变体在细菌产生EPS或执行与EPS相关功能的能力方面表现出不同程度的缺陷,证实了这些基因参与黄色黏球菌的EPS生物合成。

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