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鉴定参与脂多糖核心生物合成的rfaG、rfaP和galU基因中的Tn10插入,这些插入影响大肠杆菌的黏附。

Identification of Tn10 insertions in the rfaG, rfaP, and galU genes involved in lipopolysaccharide core biosynthesis that affect Escherichia coli adhesion.

作者信息

Genevaux P, Bauda P, DuBow M S, Oudega B

机构信息

Department of Molecular Microbiology, Faculty of Biology, Free University of Amsterdam, De Boelelaan 1087, 1081 HV, Amsterdam, The Netherlands.

出版信息

Arch Microbiol. 1999 Jul;172(1):1-8. doi: 10.1007/s002030050732.

Abstract

Escherichia coli was used as a model to study initial adhesion and early biofilm development to abiotic surface. Tn10 insertion mutants of Escherichia coli K-12 W3110 were selected for altered abilities to adhere to a polystyrene surface. Seven insertion mutants that showed a decrease in adhesion harbored insertions in genes involved in lipopolysaccharide (LPS) core biosynthesis. Two insertions were located in the rfaG gene, two in the rfaP gene, and three in the galU gene. These adhesion mutants were found to exhibit a deep-rough phenotype and to be reduced, at different levels, in type 1 fimbriae production and motility. The loss of adhesion exhibited by these mutants was associated with either the affected type 1 fimbriae production and/or the dysfunctional motility. Apart from the pleiotropic effect of the mutations affecting LPS on type 1 fimbriae and flagella biosynthesis, no evidence for an involvement of the LPS itself in adhesion to polystyrene surface could be observed.

摘要

以大肠杆菌作为模型,研究其对非生物表面的初始黏附及早期生物膜形成。通过筛选大肠杆菌K-12 W3110的Tn10插入突变体,获得了对聚苯乙烯表面黏附能力改变的突变体。七个黏附能力下降的插入突变体在参与脂多糖(LPS)核心生物合成的基因中存在插入。两个插入位于rfaG基因,两个位于rfaP基因,三个位于galU基因。这些黏附突变体表现出深粗糙表型,且1型菌毛产生和运动能力在不同程度上降低。这些突变体黏附能力的丧失与受影响的1型菌毛产生和/或功能失调的运动有关。除了影响LPS的突变对1型菌毛和鞭毛生物合成的多效性作用外,未观察到LPS本身参与对聚苯乙烯表面黏附的证据。

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