首页> 外文期刊>Molecular Microbiology >Three rhamnosyltransferases responsible for assembly of the A-band D-rhamnan polysaccharide in Pseudomonas aeruginosa: a fourth transferase, WbpL, is required for the initiation of both A-band and B-band lipopolysaccharide synthesis (published erratu
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Three rhamnosyltransferases responsible for assembly of the A-band D-rhamnan polysaccharide in Pseudomonas aeruginosa: a fourth transferase, WbpL, is required for the initiation of both A-band and B-band lipopolysaccharide synthesis (published erratu

机译:三种鼠李糖基转移酶负责铜绿假单胞菌中A带D-鼠李糖多糖的组装:第四个转移酶WbpL是引发A带和B带脂多糖合成的必需条件(已出版

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The Pseudomonas aeruginosa A-band lipopolysaccharide (LPS) molecule has an O-polysaccharide region composed of trisaccharide repeat units of alpha1-->2, alpha1-->3, alpha1-->3 linked D-rhamnose (Rha). The A-band polysaccharide is assembled by the alpha-D-rhamnosyltransferases, WbpX, WbpY and WbpZ. WbpZ probably transfers the first Rha residue onto the A-band accepting molecule, while WbpY and WbpX subsequently transfer two alpha1-->3 linked Rha residues and one alpha1-->2 linked Rha respectively. The last two transferases are predicted to be processive, alternating in their activities to complete the A-band polymer. The genes coding for these transferases were identified at the 3' end of the A-band biosynthetic cluster. Two additional genes, psecoA and uvrD, border the 3' end of the cluster and are predicted to encode a coenzyme A transferase and a DNA helicase II enzyme respectively. Chromosomal wbpX, wbpY and wbpZ mutants were generated, and Western immunoblot analysis demonstrates that these mutants are unable to synthesize A-band LPS, while B-band synthesis is unaffected. WbpL, a transferase encoded within the B-band biosynthetic cluster, was previously proposed to initiate B-band biosynthesis through the addition of Fuc2NAc (2-acetamido-2,6-dideoxy-D-galactose) to undecaprenol phosphate (Und-P). In this study, chromosomal wbpL mutants were generated that did not express A band or B band, indicating that WbpL initiates the synthesis of both LPS molecules. Cross-complementation experiments using WbpL and its homologue, Escherichia coli WecA, demonstrates that WbpL is bifunctional, initiating B-band synthesis with a Fuc2NAc residue and A-band synthesis with either a GlcNAc (N-acetylglucosamine) or GalNAc (N-acetylgalactosamine) residue. These data indicate that A-band polysaccharide assembly requires four glycosyltransferases, one of which is necessary for initiating both A-band and B-band LPS synthesis.
机译:铜绿假单胞菌A波段脂多糖(LPS)分子具有一个O-多糖区域,该区域由三糖重复单元α1-> 2,α1-> 3,α1-> 3连接的D-鼠李糖(Rha)组成。 A带多糖由α-D-鼠李糖基转移酶WbpX,WbpY和WbpZ组装。 WbpZ可能会将第一个Rha残基转移到A带接受分子上,而WbpY和WbpX随后分别转移两个alpha1-> 3连接的Rha残基和一个alpha1-> 2连接的Rha。预测最后两种转移酶是持续性的,它们的活性交替变化以完成A带聚合物。在A-带生物合成簇的3'末端鉴定了编码这些转移酶的基因。另外两个基因,psecoA和uvrD,位于簇的3'末端,预计分别编码辅酶A转移酶和DNA解旋酶II酶。产生了染色体wbpX,wbpY和wbpZ突变体,Western免疫印迹分析表明,这些突变体无法合成A波段LPS,而B波段合成则不受影响。 WbpL是一种编码在B波段生物合成簇中的转移酶,以前曾提出通过将Fuc2NAc(2-乙酰氨基-2,6-dideoxy-D-半乳糖)添加到十一碳烯醇磷酸酯(Und-P)中来启动B波段生物合成。 。在这项研究中,生成了不表达A带或B带的染色体wbpL突变体,表明WbpL启动了两个LPS分子的合成。使用WbpL及其类似物大肠杆菌WecA的交叉互补实验表明WbpL具有双功能,可通过Fuc2NAc残基启动B波段合成,并通过GlcNAc(N-乙酰氨基葡萄糖)或GalNAc(N-乙酰半乳糖胺)启动A波段合成。残留物。这些数据表明,A波段多糖组装需要四种糖基转移酶,其中之一对于启动A波段和B波段LPS合成都是必需的。

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