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幽门螺杆菌血清群O:3和O:6的脂多糖——一类脂多糖的结构,参考D-甘油-α-D-甘露庚糖残基寡聚单元的位置

Lipopolysaccharides of Helicobacter pylori serogroups O:3 and O:6--structures of a class of lipopolysaccharides with reference to the location of oligomeric units of D-glycero-alpha-D-manno-heptose residues.

作者信息

Aspinall G O, Monteiro M A, Shaver R T, Kurjanczyk L A, Penner J L

机构信息

Department of Chemistry, York University, Toronto, Ontario, Canada.

出版信息

Eur J Biochem. 1997 Sep 1;248(2):592-601. doi: 10.1111/j.1432-1033.1997.00592.x.

DOI:10.1111/j.1432-1033.1997.00592.x
PMID:9346320
Abstract

Lipopolysaccharides (LPS) from antigenically different strains assigned to serogroups O:3 and O:6 of Helicobacter pylori were isolated as water-soluble material of high Mr and as water-insoluble gels of low Mr. Chemical and spectroscopic analyses of the soluble LPS and oligosaccharides liberated from the water-insoluble gels led to proposed structures with Lewis (Le) antigen determinants terminating regular repeating units of different types, linked in turn to inner core regions of invariable structure. The O:6 LPS has two populations of related molecules with chains of 3-linked D-glycero-alpha-D-manno-heptose residues similar to those in the MO19 strain, one with and the other without a single terminal Lewis (Le(y)) epitope. In contrast, in the O:3 LPS, Lewis (Le(x) and Le(y)) epitopes terminate a partially fucosylated N-acetyllactosaminoglycan, but a heptan chain similar to that in the O:6 LPS was shown to connect the outer chains to the inner core. These LPS provide examples of the molecular mimicry of cell-surface glycoconjugates. Structural variations of LPS between strains, and differences in some aspects of structure within strains, between high Mr and low Mr LPS indicate a class of LPS whose mechanisms of biosynthesis lead to overall architectures different from those characteristic of most LPS from enteric bacteria.

摘要

从幽门螺杆菌血清群O:3和O:6的抗原性不同菌株中分离出的脂多糖(LPS),以高Mr的水溶性物质和低Mr的水不溶性凝胶形式存在。对可溶性LPS和从水不溶性凝胶中释放的寡糖进行化学和光谱分析,得出了具有Lewis(Le)抗原决定簇的结构,这些决定簇终止于不同类型的规则重复单元,进而连接到结构不变的内核区域。O:6 LPS有两类相关分子,其3-连接的D-甘油-α-D-甘露庚糖残基链与MO19菌株中的类似,一类带有单个末端Lewis(Le(y))表位,另一类没有。相比之下,在O:3 LPS中,Lewis(Le(x)和Le(y))表位终止于部分岩藻糖基化的N-乙酰乳糖胺聚糖,但一条与O:6 LPS中类似的庚糖链将外链与内核连接起来。这些LPS提供了细胞表面糖缀合物分子模拟的例子。菌株间LPS的结构变异以及同一菌株内高Mr和低Mr LPS在结构某些方面的差异表明,这类LPS的生物合成机制导致其整体结构不同于大多数肠道细菌LPS的特征结构。

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