Severn W B, Richards J C
Division of Biological Sciences, National Research Council of Canada, Ottawa, Ontario.
Carbohydr Res. 1990 Oct 10;206(2):311-32. doi: 10.1016/0008-6215(90)80070-j.
The specific capsular polysaccharide produced by Rhodococcus equi serotype 2 is a high-molecular-weight acidic polymer composed of D-glucose, D-mannose, D-glucuronic acid and 3-O-[(S)-1-carboxyethyl]-L-rhamnose in equimolar proportions. Structural analysis, employing a combination of chemical and n.m.r. techniques, established that the polysaccharide is composed of linear repeating tetrasaccharide units. (formula; see text) in which the beta-D-mannose residues carry O-acetyl groups at O-2 and O-3 to the extent of 1.7 mol equivalents. Unequivocal determination of the absolute chirality of the 3-O-[(S)-1-carboxyethyl]-alpha-L-rhamnose residues was achieved by chemical correlation with an authentic synthetic sample. The 1H and 13C-n.m.r. resonances of the native and O-deacetylated serotype 2 polysaccharides were fully assigned by homo- and heteronuclear chemical-shift correlation methods.
马红球菌2型产生的特定荚膜多糖是一种高分子量酸性聚合物,由等摩尔比例的D-葡萄糖、D-甘露糖、D-葡萄糖醛酸和3-O-[(S)-1-羧乙基]-L-鼠李糖组成。采用化学和核磁共振技术相结合的结构分析确定,该多糖由线性重复四糖单元组成。(分子式;见正文)其中β-D-甘露糖残基在O-2和O-3处带有O-乙酰基,含量为1.7摩尔当量。通过与真实合成样品的化学关联,明确确定了3-O-[(S)-1-羧乙基]-α-L-鼠李糖残基的绝对手性。通过同核和异核化学位移相关方法,完全归属了天然和O-脱乙酰化2型多糖的1H和13C核磁共振共振。