首页> 外文期刊>The Journal of biological chemistry >Identification of Novel α1,3-Galactosyltransferase and Elimination of α-Galactose-containing Glycans by Disruption of Multiple α-Galactosyltransferase Genes in Schizosaccharomyces pombe
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Identification of Novel α1,3-Galactosyltransferase and Elimination of α-Galactose-containing Glycans by Disruption of Multiple α-Galactosyltransferase Genes in Schizosaccharomyces pombe

机译:通过破坏多种α-半乳糖基转移酶基因的α1,3-半乳糖基转移酶和消除含α-半乳糖糖苷基因的α1,3-半乳糖基三族基因的鉴定

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The oligosaccharides from fission yeast Schizosaccharomyces pombe contain large amounts of d-galactose (Gal) in addition to d-mannose (Man), in contrast to the budding yeast Saccharomyces cerevisiae. Detailed structural analysis has revealed that the Gal residues are attached to the N- and O-linked oligosaccharides via α1,2- or α1,3-linkages. Previously we constructed and characterized a septuple α-galactosyltransferase disruptant (7GalTΔ) anticipating a complete lack of α-Gal residues. However, the 7GalTΔ strain still contained oligosaccharides consisting of α1,3-linked Gal residues, indicating the presence of at least one more additional unidentified α1,3-galactosyltransferase. In this study we searched for unidentified putative glycosyltransferases in the S. pombe genome sequence and identified three novel genes, named otg1+–otg3+ (α one, three-galactosyltransferase), that belong to glycosyltransferase gene family 8 in the Carbohydrate Active EnZymes (CAZY) database. Gal-recognizing lectin blotting and HPLC analyses of pyridylaminated oligosaccharides after deletion of these three additional genes from 7GalTΔ strain demonstrated that the resultant disruptant missing 10 α-galactosyltransferase genes, 10GalTΔ, exhibited a complete loss of galactosylation. In an in vitro galactosylation assay, the otg2+ gene product had Gal transfer activity toward a pyridylaminated Man9GlcNAc2 oligosaccharide and pyridylaminated Manα1,2-Manα1,2-Man oligosaccharide. In addition, the otg3+ gene product exhibited Gal transfer activity toward the pyridylaminated Man9GlcNAc2 oligosaccharide. Generation of an α1,3-linkage was confirmed by HPLC analysis, α-galactosidase digestion analysis, 1H NMR spectroscopy, and LC-MS/MS analysis. These results indicate that Otg2p and Otg3p are involved in α1,3-galactosylation of S. pombe oligosaccharides.
机译:除了D-甘露糖(MAN)外,来自裂变酵母Schizosaccharomyces Pombe的寡糖含有大量的D-半乳糖(GAL),与D-Mannose(MAN)相反,与萌芽的酵母酿酒酵母酿酒酵母相比。详细的结构分析显示GAL残基通过α1,2-或α1,3-键连接到N-和O链寡糖上。以前我们构建并表征了偏离α-半乳糖基转移酶破坏剂(7GALTδ),预期完全缺乏α-加仑残基。然而,7Galtδ菌株仍然含有由α1,3-连接的GAL残基组成的寡糖,表明存在至少一种另外的未识别的α1,3-半乳糖基转移酶。在该研究中,我们在S.Pombe基因组序列中搜索了未识别的推定糖基转移酶,并鉴定了三个名为OTG1 + -Tod3 +(α1,三半乳糖基转移酶)的三种新基因,其属于碳水化合物活性酶(聊天)中的糖基转移酶基因家族8数据库。在从7gAltδ菌株删除这三个另外的基因后,GA1识别吡啶基寡糖的副素印迹和HPLC分析证明了所得破坏剂缺失10α-半乳糖基转移酶10,10gAltΔ,表现出完全的半乳糖基化损失。在体外半乳糖基化测定中,OTG2 +基因产物具有朝向吡啶基胺的MAN9GLCNAC2寡糖和吡啶基胺化的人α1,2-MANα1,2-人寡糖的GAL转移活性。此外,OTG3 +基因产物表现出朝向吡啶基的MAN9GLCNAC2寡糖的GAL转移活性。通过HPLC分析,α-半乳糖苷酶消化分析,1H NMR光谱学和LC-MS / MS分析证实了α1,3-键的产生。这些结果表明,OTG2P和OTG3P涉及S.Pombe寡糖的α1,3-半乳糖基化。

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