Miyamoto Yuji, Mukai Tetsu, Maeda Yumi, Nakata Noboru, Kai Masanori, Naka Takashi, Yano Ikuya, Makino Masahiko
Department of Microbiology, Leprosy Research Center, National Institute of Infectious Diseases, 4-2-1 Aobacho, Higashimurayama, Tokyo 189-0002, Japan.
J Bacteriol. 2007 Aug;189(15):5515-22. doi: 10.1128/JB.00344-07. Epub 2007 May 25.
The cell envelopes of several species of nontuberculous mycobacteria, including the Mycobacterium avium complex, contain glycopeptidolipids (GPLs) as major glycolipid components. GPLs are highly antigenic surface molecules, and their variant oligosaccharides define each serotype of the M. avium complex. In the oligosaccharide portion of GPLs, the fucose residue is one of the major sugar moieties, but its biosynthesis remains unclear. To elucidate it, we focused on the 5.0-kb chromosomal region of the M. avium complex that includes five genes, two of which showed high levels of similarity to the genes involved in fucose synthesis. For the characterization of this region by deletion and expression analyses, we constructed a recombinant Mycobacterium smegmatis strain that possesses the rtfA gene of the M. avium complex to produce serovar 1 GPL. The results revealed that the 5.0-kb chromosomal region is responsible for the addition of the fucose residue to serovar 1 GPL and that the three genes mdhtA, merA, and gtfD are indispensable for the fucosylation. Functional characterization revealed that the gtfD gene encodes a glycosyltransferase that transfers a fucose residue via 1-->3 linkage to a rhamnose residue of serovar 1 GPL. The other two genes, mdhtA and merA, contributed to the formation of the fucose residue and were predicted to encode the enzymes responsible for the synthesis of fucose from mannose based on their deduced amino acid sequences. These results indicate that the fucosylation pathway in GPL biosynthesis is controlled by a combination of the mdhtA, merA, and gtfD genes. Our findings may contribute to the clarification of the complex glycosylation pathways involved in forming the oligosaccharide portion of GPLs from the M. avium complex, which are structurally distinct.
几种非结核分枝杆菌,包括鸟分枝杆菌复合群的细胞壁包膜含有糖肽脂(GPLs)作为主要的糖脂成分。GPLs是高度抗原性的表面分子,其可变寡糖定义了鸟分枝杆菌复合群的每个血清型。在GPLs的寡糖部分,岩藻糖残基是主要的糖基之一,但其生物合成仍不清楚。为了阐明这一点,我们聚焦于鸟分枝杆菌复合群的5.0 kb染色体区域,该区域包含五个基因,其中两个与岩藻糖合成相关基因具有高度相似性。为了通过缺失和表达分析来表征该区域,我们构建了一种重组耻垢分枝杆菌菌株,该菌株拥有鸟分枝杆菌复合群的rtfA基因以产生血清型1 GPL。结果表明,5.0 kb染色体区域负责将岩藻糖残基添加到血清型1 GPL中,并且mdhtA、merA和gtfD这三个基因对于岩藻糖基化是必不可少的。功能表征表明,gtfD基因编码一种糖基转移酶,该酶通过1→3连接将岩藻糖残基转移到血清型1 GPL的鼠李糖残基上。另外两个基因mdhtA和merA有助于岩藻糖残基的形成,根据其推导的氨基酸序列预测它们编码负责从甘露糖合成岩藻糖的酶。这些结果表明,GPL生物合成中的岩藻糖基化途径受mdhtA、merA和gtfD基因的组合控制。我们的发现可能有助于阐明参与从结构不同的鸟分枝杆菌复合群形成GPLs寡糖部分的复杂糖基化途径。