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铜绿假单胞菌Psl胞外多糖的遗传和生化分析揭示了多糖合成酶在Psl和脂多糖产生中的重叠作用。

Genetic and biochemical analyses of the Pseudomonas aeruginosa Psl exopolysaccharide reveal overlapping roles for polysaccharide synthesis enzymes in Psl and LPS production.

作者信息

Byrd Matthew S, Sadovskaya Irina, Vinogradov Evgueny, Lu Haiping, Sprinkle April B, Richardson Stephen H, Ma Luyan, Ralston Brad, Parsek Matthew R, Anderson Erin M, Lam Joseph S, Wozniak Daniel J

机构信息

Department of Microbiology and Immunology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

Mol Microbiol. 2009 Aug;73(4):622-38. doi: 10.1111/j.1365-2958.2009.06795.x. Epub 2009 Jul 29.

DOI:10.1111/j.1365-2958.2009.06795.x
PMID:19659934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4409829/
Abstract

Exopolysaccharides contribute significantly to attachment and biofilm formation in the opportunisitc pathogen Pseudomonas aeruginosa. The Psl polysaccharide, which is synthesized by the polysaccharide synthesis locus (psl), is required for biofilm formation in non-mucoid strains that do not rely on alginate as the principal biofilm polysaccharide. In-frame deletion and complementation studies of individual psl genes revealed that 11 psl genes, pslACDEFGHIJKL, are required for Psl production and surface attachment. We also present the first structural analysis of the psl-dependent polysaccharide, which consists of a repeating pentasaccharide containing d-mannose, d-glucose and l-rhamnose: [See text]. In addition, we identified the sugar nucleotide precursors involved in Psl generation and demonstrated the requirement for GDP-d-mannose, UDP-d-glucose and dTDP-l-rhamnose in Psl production and surface attachment. Finally, genetic analyses revealed that wbpW restored Psl production in a pslB mutant and pslB promoted A-band LPS synthesis in a wbpW mutant, indicating functional redundancy and overlapping roles for these two enzymes. The structural and genetic data presented here provide a basis for further investigation of the Psl proteins and potential roles for Psl in the biology and pathogenesis of P. aeruginosa.

摘要

胞外多糖对机会致病菌铜绿假单胞菌的附着和生物膜形成有重要作用。由多糖合成位点(psl)合成的Psl多糖,对于不依赖藻酸盐作为主要生物膜多糖的非黏液型菌株的生物膜形成是必需的。对单个psl基因进行框内缺失和互补研究表明,11个psl基因,即pslACDEFGHIJKL,对于Psl的产生和表面附着是必需的。我们还首次对依赖psl的多糖进行了结构分析,该多糖由包含d-甘露糖、d-葡萄糖和l-鼠李糖的重复五糖组成:[见正文]。此外,我们确定了参与Psl生成的糖核苷酸前体,并证明了GDP-d-甘露糖、UDP-d-葡萄糖和dTDP-l-鼠李糖在Psl产生和表面附着中的必要性。最后,遗传分析表明,wbpW在pslB突变体中恢复了Psl的产生,而pslB在wbpW突变体中促进了A带脂多糖的合成,这表明这两种酶具有功能冗余和重叠作用。本文提供的结构和遗传数据为进一步研究Psl蛋白以及Psl在铜绿假单胞菌生物学和发病机制中的潜在作用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7117/4409829/5bed51ca874f/nihms134883f9.jpg
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