Jeevarajah Dharshini, Patterson John H, McConville Malcolm J, Billman-Jacobe Helen
Departments of Microbiology and Immunology1, and Biochemistry and Molecular Biology2, University of Melbourne, Victoria 3010, Australia.
Microbiology (Reading). 2002 Oct;148(Pt 10):3079-3087. doi: 10.1099/00221287-148-10-3079.
Glycopeptidolipids (GPLs) are a major component of the outer layers of the cell walls of several non-tuberculous mycobacteria. The Mycobacterium smegmatis GPLs consist of a diglycosylated lipopeptide core which is variably modified by acetylation and methylation. Analysis of a region of the M. smegmatis chromosome, upstream of the peptide synthetase gene, mps, revealed a GPL biosynthetic locus containing genes potentially involved in glycosylation, methylation, acetylation and transport of GPLs. Methyltransferases are required to modify rhamnose and the fatty acid of GPLs. Of the four methyltransferases encoded within the locus, one methyltransferase, Mtf2, was unlike sugar methyltransferases from other species. An mtf2 mutant was created and was shown to be unable to methylate the GPL fatty acids. Direct evidence is presented that Mtf2 is a methyltransferase that modifies the GPL fatty acid.
糖肽脂(GPLs)是几种非结核分枝杆菌细胞壁外层的主要成分。耻垢分枝杆菌的GPLs由一个双糖基化脂肽核心组成,该核心会被乙酰化和甲基化进行不同程度的修饰。对耻垢分枝杆菌染色体上肽合成酶基因mps上游区域的分析揭示了一个GPL生物合成位点,其中包含可能参与GPL糖基化、甲基化、乙酰化和转运的基因。甲基转移酶是修饰GPL鼠李糖和脂肪酸所必需的。在该位点编码的四种甲基转移酶中,有一种甲基转移酶Mtf2,与其他物种的糖甲基转移酶不同。构建了一个mtf2突变体,结果表明它无法使GPL脂肪酸甲基化。直接证据表明Mtf2是一种修饰GPL脂肪酸的甲基转移酶。