Rutherford T J, Jones C, Davies D B, Elliott A C
Chemistry Division, National Institute for Biological Standards & Control, Hertfordshire, Great Britain.
Carbohydr Res. 1991 Sep 30;218:175-84. doi: 10.1016/0008-6215(91)84096-w.
The 1H-n.m.r. spectra of the Streptococcus pneumoniae type 9V (S68 in American nomenclature) capsular polysaccharide (PS) and its O-deacetylated derivative [which is structurally identical to the S. pneumoniae type 9A (S33) PS] were assigned using COSY, relayed-COSY, and 2D-NOESY experiments. The positions of the OAc groups in the alpha-GlcA, beta-ManNAc, and alpha-Glc residues of the native 9V PS were established using 2D-n.m.r. and chemical shift arguments, and the relative proportions of different O-acetylated species were estimated by integration of well-resolved 1H-n.m.r. signals. The locations of the OAc substituents differ from those previously reported. [formula: see text].
运用COSY、接力COSY和二维核Overhauser效应光谱(2D-NOESY)实验,对9V型肺炎链球菌(美国命名法中的S68)荚膜多糖(PS)及其O-脱乙酰化衍生物[其结构与9A型肺炎链球菌(S33)PS相同]的1H-核磁共振光谱进行了归属。利用二维核磁共振和化学位移论证确定了天然9V PS的α-葡萄糖醛酸(α-GlcA)、β-甘露糖胺(β-ManNAc)和α-葡萄糖(α-Glc)残基中OAc基团的位置,并通过对分辨率良好的1H-核磁共振信号进行积分,估算了不同O-乙酰化物种的相对比例。OAc取代基的位置与先前报道的不同。[化学式:见原文]