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鉴定黄色粘球菌孢子衣多糖生物合成中的 Wzx 翻转酶、Wzy 聚合酶和糖修饰酶。

Identification of the Wzx flippase, Wzy polymerase and sugar-modifying enzymes for spore coat polysaccharide biosynthesis in Myxococcus xanthus.

机构信息

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.

出版信息

Mol Microbiol. 2020 Jun;113(6):1189-1208. doi: 10.1111/mmi.14486. Epub 2020 Feb 25.

Abstract

The rod-shaped cells of Myxococcus xanthus, a Gram-negative deltaproteobacterium, differentiate to environmentally resistant spores upon starvation or chemical stress. The environmental resistance depends on a spore coat polysaccharide that is synthesised by the ExoA-I proteins, some of which are part of a Wzx/Wzy-dependent pathway for polysaccharide synthesis and export; however, key components of this pathway have remained unidentified. Here, we identify and characterise two additional loci encoding proteins with homology to enzymes involved in polysaccharide synthesis and export, as well as sugar modification and show that six of the proteins encoded by these loci are essential for the formation of environmentally resistant spores. Our data support that MXAN_3260, renamed ExoM and MXAN_3026, renamed ExoJ, are the Wzx flippase and Wzy polymerase, respectively, responsible for translocation and polymerisation of the repeat unit of the spore coat polysaccharide. Moreover, we provide evidence that three glycosyltransferases (MXAN_3027/ExoK, MXAN_3262/ExoO and MXAN_3263/ExoP) and a polysaccharide deacetylase (MXAN_3259/ExoL) are important for formation of the intact spore coat, while ExoE is the polyisoprenyl-phosphate hexose-1-phosphate transferase responsible for initiating repeat unit synthesis, likely by transferring N-acetylgalactosamine-1-P to undecaprenyl-phosphate. Together, our data generate a more complete model of the Exo pathway for spore coat polysaccharide biosynthesis and export.

摘要

黄色粘球菌(Myxococcus xanthus)是革兰氏阴性 δ-变形菌,其杆状细胞在饥饿或化学胁迫时会分化为具有环境抗性的孢子。环境抗性取决于由 ExoA-I 蛋白合成的孢子被膜多糖,其中一些蛋白是多糖合成和外排的 Wzx/Wzy 依赖途径的一部分;然而,该途径的关键成分仍未被鉴定。在这里,我们鉴定并描述了两个额外的编码与多糖合成和外排、糖修饰相关酶同源蛋白的基因座,并表明这些基因座编码的 6 种蛋白对于形成具有环境抗性的孢子是必需的。我们的数据支持 MXAN_3260(重新命名为 ExoM)和 MXAN_3026(重新命名为 ExoJ)分别是 Wzx 翻转酶和 Wzy 聚合酶,负责重复单位的转位和多糖的聚合。此外,我们提供的证据表明,三个糖基转移酶(MXAN_3027/ExoK、MXAN_3262/ExoO 和 MXAN_3263/ExoP)和一个多糖脱乙酰酶(MXAN_3259/ExoL)对于完整孢子被膜的形成很重要,而 ExoE 是聚异戊二烯磷酸己糖-1-磷酸转移酶,负责重复单元合成的起始,可能是通过将 N-乙酰半乳糖胺-1-P 转移到十一碳烯磷酸上。总之,我们的数据为 Exo 途径合成和外排孢子被膜多糖提供了一个更完整的模型。

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