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rml基因座参与铜绿假单胞菌核心寡糖和O抗原多糖的组装过程。

Involvement of the rml locus in core oligosaccharide and O polysaccharide assembly in Pseudomonas aeruginosa.

作者信息

Rahim Rahim, Burrows Lori L, Monteiro Mario A, Perry Malcolm B, Lam Joseph S

机构信息

Canadian Bacterial Diseases Network, Networks of Centers of Excellence, Heritage Medical Research Building, Hospital Drive, Calgary, Alberta, Canada T2N 4N12.

Department of Microbiology, University of Guelph, Guelph, Ontario, Canada, N1G 2W11.

出版信息

Microbiology (Reading). 2000 Nov;146 ( Pt 11):2803-2814. doi: 10.1099/00221287-146-11-2803.

Abstract

L-Rhamnose (L-Rha) is a component of the lipopolysaccharide (LPS) core, several O antigen polysaccharides, and the cell surface surfactant rhamnolipid of Pseudomonas aeruginosa. In this study, four contiguous genes (rmlBDAC) responsible for the synthesis of dTDP-L-Rha in P. aeruginosa have been cloned and characterized. Non-polar chromosomal rmlC mutants were generated in P. aeruginosa strains PAO1 (serotype O5) and PAK (serotype O6) and LPS extracted from the mutants was analysed by SDS-PAGE and Western immunoblotting. rmlC mutants of both serotype O5 and serotype O6 synthesized a truncated core region which was unable to act as an attachment point for either A-band or B-band O antigen. A rmd rmlC PAO1 double mutant (deficient in biosynthesis of both D-Rha and L-Rha) was constructed to facilitate structural analysis of the mutant core region. This strain has an incomplete core oligosaccharide region and does not produce A-band O antigen. These results provide the genetic and structural evidence that L-Rha is the receptor on the P. aeruginosa LPS core for the attachment of O polysaccharides. This is the first report of a genetically defined mutation that affects the synthesis of a single sugar in the core oligosaccharide region of P. aeruginosa LPS, and provides further insight into the mechanisms of LPS biosynthesis and assembly in this bacterium.

摘要

L-鼠李糖(L-Rha)是铜绿假单胞菌脂多糖(LPS)核心、几种O抗原多糖以及细胞表面活性剂鼠李糖脂的组成成分。在本研究中,已克隆并鉴定了铜绿假单胞菌中负责合成dTDP-L-Rha的四个相邻基因(rmlBDAC)。在铜绿假单胞菌菌株PAO1(血清型O5)和PAK(血清型O6)中产生了非极性染色体rmlC突变体,并通过SDS-PAGE和Western免疫印迹分析了从突变体中提取的LPS。血清型O5和血清型O6的rmlC突变体均合成了截短的核心区域,该区域无法作为A带或B带O抗原的附着点。构建了rmd rmlC PAO1双突变体(缺乏D-Rha和L-Rha的生物合成)以促进对突变核心区域的结构分析。该菌株具有不完整的核心寡糖区域,不产生A带O抗原。这些结果提供了遗传和结构证据,表明L-Rha是铜绿假单胞菌LPS核心上O多糖附着的受体。这是关于影响铜绿假单胞菌LPS核心寡糖区域中单一糖合成的基因定义突变的首次报道,并为该细菌中LPS生物合成和组装的机制提供了进一步的见解。

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