Yildirim Håkan H, Li Jianjun, Richards James C, Hood Derek W, Moxon E Richard, Schweda Elke K H
Clinical Research Centre, Karolinska Institutet and University College of South Stockholm, NOVUM, S-141 86 Huddinge, Sweden.
Biochemistry. 2005 Apr 5;44(13):5207-24. doi: 10.1021/bi047480h.
Common structural motifs of Haemophilus influenzae lipopolysaccharide (LPS) are globotetraose [beta-d-GalpNAc-(1-->3)-alpha-d-Galp-(1-->4)-beta-d-Galp-(1-->4)-beta-d-Glcp] and its truncated versions globoside [alpha-d-Galp-(1-->4)-beta-d-Galp-(1-->4)-beta-d-Glcp] and lactose [beta-d-Galp-(1-->4)-beta-d-Glcp] linked to the terminal heptose (HepIII) of the triheptosyl inner-core moiety l-alpha-d-Hepp-(1-->2)-[PEA-->6]-l-alpha-d-Hepp-(1-->3)-l-alpha-d-Hepp-(1-->5)-[PPEA-->4]-alpha-Kdo-(2-->6)-lipid A. We report here structural studies of LPS from nontypeable H. influenzae strain 1124 expressing these motifs linked to both the proximal heptose (HepI) and HepIII at the same time. This novel finding was obtained by structural studies of LPS using NMR techniques and electrospray ionization mass spectrometry (ESI-MS) on O-deacylated LPS and core oligosaccharide material (OS) as well as ESI-MS(n)() on permethylated dephosphorylated OS. The use of defined mutants allowed us to confirm structures unambiguously and understand better the biosynthesis of each of the globotetraose units. We found that lgtC is involved in the expression of alpha-d-Galp-(1-->4)-beta-d-Galp in both extensions, whereas lic2A directs only the expression of beta-d-Galp-(1-->4)-beta-d-Glcp when linked to HepIII. The LPS of NTHi strain 1124 contained sialylated glycoforms that were identified by CE-ESI-MS/MS. A common sialylated structure in H. influenzae LPS is sialyllactose linked to HepIII. This structure exists in strain 1124. However, results for the lpsA mutant indicate that sialyllactose extends from HepI as well, a molecular environment for sialyllactose in H. influenzae that has not been reported previously. In addition, the LPS was found to carry phosphorylcholine, O-linked glycine, and a third PEA group which was linked to O3 of HepIII.
流感嗜血杆菌脂多糖(LPS)的常见结构基序是球四糖[β - d - 氨基半乳糖 - (1→3) - α - d - 半乳糖 - (1→4) - β - d - 半乳糖 - (1→4) - β - d - 葡萄糖]及其截短形式球苷[α - d - 半乳糖 - (1→4) - β - d - 半乳糖 - (1→4) - β - d - 葡萄糖]和乳糖[β - d - 半乳糖 - (1→4) - β - d - 葡萄糖],它们连接到三庚糖基内核部分l - α - d - 庚糖 - (1→2) - [PEA→6] - l - α - d - 庚糖 - (1→3) - l - α - d - 庚糖 - (1→5) - [PPEA→4] - α - Kdo - (2→6) - 脂质A的末端庚糖(HepIII)上。我们在此报告了对不可分型流感嗜血杆菌菌株1124的LPS的结构研究,该菌株同时表达与近端庚糖(HepI)和HepIII相连的这些基序。这一新颖发现是通过对LPS进行结构研究获得的,采用了核磁共振技术和电喷雾电离质谱(ESI - MS)对O - 脱酰化LPS和核心寡糖物质(OS)进行分析,以及对全甲基化去磷酸化OS进行ESI - MS(n)()分析。使用特定的突变体使我们能够明确确认结构,并更好地理解每个球四糖单元的生物合成。我们发现lgtC参与了两个延伸部分中α - d - 半乳糖 - (1→4) - β - d - 半乳糖的表达,而lic2A仅在与HepIII相连时指导β - d - 半乳糖 - (1→4) - β - d - 葡萄糖的表达。NTHi菌株1124的LPS包含经CE - ESI - MS/MS鉴定的唾液酸化糖型。流感嗜血杆菌LPS中一种常见的唾液酸化结构是连接到HepIII的唾液乳糖。这种结构存在于菌株1124中。然而,lpsA突变体的结果表明唾液乳糖也从HepI延伸,这是流感嗜血杆菌中唾液乳糖的一种此前未报道过的分子环境。此外,发现该LPS带有磷酸胆碱、O - 连接的甘氨酸以及连接到HepIII的O3上的第三个PEA基团。