Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91 Stockholm, Sweden.
Carbohydr Res. 2011 Oct 18;346(14):2300-3. doi: 10.1016/j.carres.2011.06.022. Epub 2011 Jun 25.
The structure of the O-antigen polysaccharide (PS) from Escherichia coli O177 has been determined. Component analysis together with (1)H and (13)C NMR spectroscopy experiments was used to determine the structure. Inter-residue correlations were determined by (1)H,(13)C-heteronuclear multiple-bond correlation and (1)H,(1)H-NOESY experiments. PS is composed of tetrasaccharide repeating units with the following structure: →2)-α-L-Rhap-(1→3)-α-L-FucpNAc-(1→3)-α-L-FucpNAc-(1→3)-β-D-GlcpNAc-(1→. An α-L-Rhap residue is suggested to be present at the terminal part of the polysaccharide, which on average is composed of ∼20 repeating units, since the (1)H and (13)C chemical shifts of an α-linked rhamnopyranosyl group could be assigned by a combination of 2D NMR spectra. Consequently, the biological repeating unit has a 3-substituted N-acetyl-D-glucosamine residue at its reducing end. The repeating unit of the E. coli O177 O-antigen shares the →3)-α-L-FucpNAc-(1→3)-β-D-GlcpNAc-(1→ structural element with the O-antigen from E. coli O15 and this identity may then explain the reported cross-reactivity between the strains.
已确定大肠杆菌 O177 的 O-抗原多糖 (PS) 的结构。通过成分分析和 (1)H 和 (13)C NMR 光谱实验来确定结构。通过 (1)H、(13)C-异核多键相关和 (1)H、(1)H-NOESY 实验确定了残基间的相关性。PS 由四糖重复单元组成,具有以下结构:→2)-α-L-Rhap-(1→3)-α-L-FucpNAc-(1→3)-α-L-FucpNAc-(1→3)-β-D-GlcpNAc-(1→。由于可以通过二维 NMR 光谱的组合来分配α-连接的鼠李吡喃糖基的 (1)H 和 (13)C 化学位移,因此建议在多糖的末端存在α-L-Rhap 残基,其平均由约 20 个重复单元组成。因此,生物重复单元在其还原端具有 3-取代的 N-乙酰-D-葡糖胺残基。大肠杆菌 O177 O-抗原的重复单元与大肠杆菌 O15 的 O-抗原共享→3)-α-L-FucpNAc-(1→3)-β-D-GlcpNAc-(1→结构单元,这种同一性可能解释了这两个菌株之间报道的交叉反应性。