Kobayashi H, Mitobe H, Takahashi K, Yamamoto T, Shibata N, Suzuki S
Second Department of Hygienic Chemistry, Tohoku College of Pharmacy, Miyagi, Japan.
Arch Biochem Biophys. 1992 May 1;294(2):662-9. doi: 10.1016/0003-9861(92)90739-j.
We conducted a structural analysis of the cell wall mannan-protein complex (mannan) isolated from a pathogenic yeast, Candida glabrata IFO 0622 strain. The chemical structure of mannobiose released from this mannan by treatment with 10 mM HCl at 100 degrees C for 1 h was identified as Manp beta 1-2Man. The treatment of this mannan with 100 mM NaOH at 25 degrees C for 18 h gave a mixture of alpha-1,2- and alpha-1,3-linked oligosaccharides, from tetraose to biose, and mannose. The acid- and alkali-stable mannan moiety was subjected to mild acetolysis with a 100:100:1 (v/v) mixture of (CH3CO)2O, CH3COOH, and H2SO4 at 40 degrees C for 36 h. The resultant three novel oligosaccharides, tetraose, hexaose, and heptaose, were identified as Manp beta 1-2Manp alpha 1-2Manp alpha 1-2Man, Manp alpha 1-2Manp alpha 1-2Manp alpha 1-6Manp alpha 1-2Manp alpha 1-2Man, and Manp alpha 1-3Manp alpha 1-2Manp alpha 1-2Manp alpha 1-6Manp alpha 1- 2Manp alpha 1-2Man, respectively, in addition to the three known oligosaccharides, Manp alpha 1-2Man, Manp alpha 1-2Manp alpha 1-2Man, and Manp alpha 1-3Manp alpha 1-2Manp alpha 1-2Man. A sequential analytical procedure involving partial acid hydrolysis with hot 0.3 M H2SO4, methylation, fast atom bombardment mass, and 1H NMR analyses was quite effective in the structural determination of the novel oligosaccharides. The results indicate that this mannan possesses a structure closely resembling that of Saccharomyces cerevisiae X2180-1A wild type strain, with the presence of small amounts of oligomannosyl residue, Manp beta 1-2Manp alpha 1-X, corresponding to one of the epitopes dominating serotype-A specificity of Candida spp., in addition to branches corresponding to hexaose and heptaose each containing one intermediary alpha-1,6 linkage.
我们对从致病性酵母光滑念珠菌IFO 0622菌株中分离出的细胞壁甘露聚糖 - 蛋白质复合物(甘露聚糖)进行了结构分析。通过在100℃下用10 mM HCl处理该甘露聚糖1小时释放出的甘露二糖的化学结构被鉴定为Manpβ1 - 2Man。在25℃下用100 mM NaOH处理该甘露聚糖18小时,得到了从四糖到二糖的α - 1,2 - 和α - 1,3 - 连接的寡糖混合物以及甘露糖。将酸和碱稳定的甘露聚糖部分在40℃下用(CH3CO)2O、CH3COOH和H2SO4的100:100:1(v/v)混合物进行温和乙酰解36小时。除了三种已知的寡糖Manpα1 - 2Man、Manpα1 - 2Manpα1 - 2Man和Manpα1 - 3Manpα1 - 2Manpα1 - 2Man外,所得的三种新型寡糖,四糖、六糖和七糖,分别被鉴定为Manpβ1 - 2Manpα1 - 2Manpα1 - 2Man、Manpα1 - 2Manpα1 - 2Manpα1 - 6Manpα1 - 2Manpα1 - 2Man和Manpα1 - 3Manpα1 - 2Manpα1 - 2Manpα1 - 6Manpα1 - 2Manpα1 - 2Man。涉及用热的0.3 M H2SO4进行部分酸水解、甲基化、快原子轰击质谱和1H NMR分析的顺序分析程序在新型寡糖的结构测定中非常有效。结果表明,这种甘露聚糖具有与酿酒酵母X2180 - 1A野生型菌株非常相似的结构,除了分别含有一个中间α - 1,6连接的六糖和七糖的分支外,还存在少量对应于念珠菌属血清型 - A特异性主导表位之一的低聚甘露糖基残基Manpβ1 - 2Manpα1 - X。