Kelly John, Jarrell Harold, Millar Lorna, Tessier Luc, Fiori Laura M, Lau Peter C, Allan Brenda, Szymanski Christine M
Institute for Biological Sciences, National Research Council, 100 Sussex Dr., Ottawa, Ontario K1A 0R6, Canada.
J Bacteriol. 2006 Apr;188(7):2427-34. doi: 10.1128/JB.188.7.2427-2434.2006.
In eukaryotes, N-linked protein glycosylation is a universal modification involving addition of preformed oligosaccharides to select Asn-Xaa-Ser/Thr motifs and influencing multiple biological events. We recently demonstrated that Campylobacter jejuni is the first member of the Bacteria to possess an N-linked glycan pathway. In this study, high-resolution magic angle spinning nuclear magnetic resonance (HR-MAS NMR) was applied to probe and quantitate C. jejuni N-glycan biosynthesis in vivo. To confirm HR-MAS NMR findings, glycosylation mutants were screened for chicken colonization potential, and glycoproteins were examined by mass spectrometry and lectin blotting. Consistent with the mechanism in eukaryotes, the combined data indicate that bacterial glycans are assembled en bloc, emphasizing the evolutionary conservation of protein N glycosylation. We also show that under the conditions examined, PglG plays no role in glycan biosynthesis, PglI is the glucosyltransferase and the putative ABC transporter, and WlaB (renamed PglK) is required for glycan assembly. These studies underpin the mechanism of N-linked protein glycosylation in Bacteria and provide a simple model system for investigating protein glycosylation and for exploitation in glycoengineering.
在真核生物中,N-连接的蛋白质糖基化是一种普遍的修饰,涉及将预先形成的寡糖添加到特定的天冬酰胺-任意氨基酸-丝氨酸/苏氨酸基序上,并影响多种生物学事件。我们最近证明,空肠弯曲菌是细菌中首个拥有N-连接聚糖途径的成员。在本研究中,高分辨率魔角旋转核磁共振(HR-MAS NMR)被用于探测和定量空肠弯曲菌体内的N-聚糖生物合成。为了证实HR-MAS NMR的结果,对糖基化突变体进行了鸡定植潜力筛选,并通过质谱和凝集素印迹法对糖蛋白进行了检测。与真核生物中的机制一致,综合数据表明细菌聚糖是整体组装的,强调了蛋白质N-糖基化的进化保守性。我们还表明,在所研究的条件下,PglG在聚糖生物合成中不起作用,PglI是葡糖基转移酶和假定的ABC转运蛋白,而WlaB(重新命名为PglK)是聚糖组装所必需的。这些研究巩固了细菌中N-连接蛋白质糖基化的机制,并为研究蛋白质糖基化以及在糖工程中的应用提供了一个简单的模型系统。