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分枝杆菌中 mycolic acid 生物合成的新成员 Cg1246

Cg1246, a new player in mycolic acid biosynthesis in .

机构信息

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France.

Institut de Pharmacologie et de Biologie Structurale, IPBS, Université de Toulouse, CNRS, UPS, Toulouse, France.

出版信息

Microbiology (Reading). 2022 Apr;168(4). doi: 10.1099/mic.0.001171.

DOI:10.1099/mic.0.001171
PMID:35394419
Abstract

Mycolic acids are key components of the complex cell envelope of . These fatty acids, conjugated to trehalose or to arabinogalactan form the backbone of the mycomembrane. While mycolic acids are essential to the survival of some species, such as , their absence is not lethal for which has been extensively used as a model to depict their biosynthesis. Mycolic acids are first synthesized on the cytoplasmic side of the inner membrane and transferred onto trehalose to give trehalose monomycolate (TMM). TMM is subsequently transported to the periplasm by dedicated transporters and used by mycoloyltransferase enzymes to synthesize all the other mycolate-containing compounds. Using a random transposition mutagenesis, we recently identified a new uncharacterized protein (Cg1246) involved in mycolic acid metabolism. Cg1246 belongs to the DUF402 protein family that contains some previously characterized nucleoside phosphatases. In this study, we performed a functional and structural characterization of Cg1246. We showed that absence of the protein led to a significant reduction in the pool of TMM in , resulting in a decrease in all other mycolate-containing compounds. We found that, , Cg1246 has phosphatase activity on organic pyrophosphate substrates but is most likely not a nucleoside phosphatase. Using a computational approach, we identified important residues for phosphatase activity and constructed the corresponding variants in . Surprisingly complementation with these non-functional proteins fully restored the defect in TMM of the Δ mutant strain, suggesting that , the phosphatase activity is not involved in mycolic acid biosynthesis.

摘要

分枝菌酸是复杂细胞包膜的关键成分。这些脂肪酸与海藻糖或阿拉伯半乳聚糖结合,构成了菌膜的骨架。虽然分枝菌酸对某些物种的生存至关重要,如分枝杆菌,但它们的缺失对结核分枝杆菌并不致命,结核分枝杆菌已被广泛用作描绘其生物合成的模型。分枝菌酸最初在内膜的细胞质侧合成,并转移到海藻糖上形成海藻糖单酯(TMM)。TMM 随后通过专用转运蛋白转运到周质,并被酰基转移酶用于合成所有其他含分枝菌酸的化合物。通过随机转座诱变,我们最近鉴定了一种新的未被表征的分枝菌酸代谢相关蛋白(Cg1246)。Cg1246 属于 DUF402 蛋白家族,该家族包含一些以前被表征的核苷磷酸酶。在本研究中,我们对 Cg1246 进行了功能和结构表征。我们发现该蛋白缺失会导致细胞内 TMM 池显著减少,导致所有其他含分枝菌酸的化合物减少。我们发现,Cg1246 对有机焦磷酸盐底物具有磷酸酶活性,但不太可能是核苷磷酸酶。通过计算方法,我们确定了磷酸酶活性的重要残基,并在构建了相应的变体。令人惊讶的是,这些非功能性蛋白的互补完全恢复了Δ突变株中 TMM 的缺陷,这表明,磷酸酶活性不参与分枝菌酸的生物合成。

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