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Identification of the Missing trans-Acting Enoyl Reductase Required for Phthiocerol Dimycocerosate and Phenolglycolipid Biosynthesis in Mycobacterium tuberculosis▿ †

机译:鉴定结核分枝杆菌中的苯二酚二霉菌酸酯和苯酚糖脂的生物合成所需的缺失的反式烯丙基还原酶▿†

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摘要

Phthiocerol dimycocerosates (DIM) and phenolglycolipids (PGL) are functionally important surface-exposed lipids of Mycobacterium tuberculosis. Their biosynthesis involves the products of several genes clustered in a 70-kb region of the M. tuberculosis chromosome. Among these products is PpsD, one of the modular type I polyketide synthases responsible for the synthesis of the lipid core common to DIM and PGL. Bioinformatic analyses have suggested that this protein lacks a functional enoyl reductase activity domain required for the synthesis of these lipids. We have identified a gene, Rv2953, that putatively encodes an enoyl reductase. Mutation in Rv2953 prevents conventional DIM formation and leads to the accumulation of a novel DIM-like product. This product is unsaturated between C-4 and C-5 of phthiocerol. Consistently, complementation of the mutant with a functional pks15/1 gene from Mycobacterium bovis BCG resulted in the accumulation of an unsaturated PGL-like substance. When an intact Rv2953 gene was reintroduced into the mutant strain, the phenotype reverted to the wild type. These findings indicate that Rv2953 encodes a trans-acting enoyl reductase that acts with PpsD in phthiocerol and phenolphthiocerol biosynthesis.
机译:苯二酚二腰果酸酯(DIM)和酚糖脂(PGL)是结核分枝杆菌在功能上重要的表面暴露脂质。它们的生物合成涉及结核分枝杆菌染色体70-kb区域中的几个基因的产物。在这些产品中有PpsD,它是负责合成DIM和PGL共有的脂质核心的一种模块化I型聚酮化合物合酶。生物信息学分析表明,该蛋白质缺乏合成这些脂质所需的功能性烯基还原酶活性域。我们已经鉴定出一个基因Rv2953,该基因假定编码烯酰还原酶。 Rv2953中的突变阻止了常规DIM的形成,并导致了新型DIM样产物的积累。该产物在苯硫酚的C-4和C-5之间是不饱和的。一致地,突变体与来自牛分枝杆菌BCG的功能性pks15 / 1基因的互补导致不饱和PGL样物质的积累。当将完整的Rv2953基因重新引入突变株后,该表型恢复为野生型。这些发现表明,Rv2953编码一种反式烯酰还原酶,该酶在苯硫酚和酚苯硫酚的生物合成中与PpsD相互作用。

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