Institute for Biological Sciences, National Research Council, Ottawa, ON, K1A 0R6, Canada.
Glycobiology. 2009 Dec;19(12):1436-45. doi: 10.1093/glycob/cwp117. Epub 2009 Aug 8.
Previous studies on LPS from Neisseria meningitidis strains M992B, the immunotype L6 strain, NMB, the type strain, a candidate LPS vaccine strain 6275z, and an extensively used clinical strain M986 had suggested that the location of the phosphoethanolamine (PEtn) residue was the 7-position of the distal heptose residue (HepII) of the inner-core oligosaccharide (OS). In all cases, this was only established by chemical methods, methylation linkage analyses. In this study, we have used standard NMR techniques to unequivocally show that the PEtn residue is actually located at the 6-position and not at the 7-position of the HepII residue in all of these strains. The 6-PEtn transferase genes were sequenced and their translated amino acid sequences were shown to be greater than 96% identical to that of the Lpt6 transferase from the L4 immunotype strain, which has been shown to transfer PEtn to the 6-position of the distal heptose residue. We discuss the implications of these findings with respect to the immunotyping scheme for the meningococci and in the context of LPS-based vaccine development.
先前针对脑膜炎奈瑟菌 M992B 菌株、免疫型 L6 菌株、NMB(模式株)、候选脂多糖疫苗菌株 6275z 以及一种广泛应用的临床菌株 M986 的 LPS 研究表明,磷酸乙醇胺(PEtn)残基的位置位于核心寡糖(OS)的远端庚糖残基(HepII)的 7 位。在所有情况下,这仅通过化学方法、甲基化键合分析来确定。在这项研究中,我们使用标准 NMR 技术明确表明,在所有这些菌株中,PEtn 残基实际上位于 HepII 残基的 6 位,而不是 7 位。6-PEtn 转移酶基因被测序,其翻译的氨基酸序列与 L4 免疫型菌株的 Lpt6 转移酶的氨基酸序列大于 96%相同,该酶已被证明将 PEtn 转移到远端庚糖残基的 6 位。我们讨论了这些发现对脑膜炎奈瑟菌免疫分型方案以及基于 LPS 的疫苗开发的影响。