Ohe Y, Ohtani K, Sone Y, Misaki A
Department of Food and Nutrition, Faculty of Science of Living, Osaka City University, Japan.
Biosci Biotechnol Biochem. 1993 Feb;57(2):227-30. doi: 10.1271/bbb.57.227.
Alfa-D-glucans containing a 3,6-anhydro D-glucosyl residue were prepared from three kinds of alpha-D-glucan (elsinan, pullulan, and amylose), and the physical properties of these 3,6-anhydro glucans were examined. The method employed for introducing the 3,6-anhydro linkage into a D-glucosyl residue involved sulfation of the O-6 position with dimethylsulfoxide-sulfur trioxide complex and a subsequent alkali treatment of the resulting partially sulfated glucan. This introduction of the 3,6-anhydro linkage caused a decrease in viscosity of the original polysaccharides and made them resistant to the action of hydrolytic enzymes. Hydrolysis of the 3,6-anhydro glucans with dilute acid afforded several oligosaccharides whose reducing end was 3,6-anhydro D-glucose.
从三种α-D-葡聚糖(埃尔辛南、支链淀粉和直链淀粉)制备了含有3,6-脱水-D-葡糖基残基的α-D-葡聚糖,并研究了这些3,6-脱水葡聚糖的物理性质。将3,6-脱水键引入D-葡糖基残基的方法包括用二甲基亚砜-三氧化硫络合物对O-6位进行硫酸化,以及随后对所得部分硫酸化的葡聚糖进行碱处理。这种3,6-脱水键的引入导致原始多糖的粘度降低,并使其对水解酶的作用具有抗性。用稀酸水解3,6-脱水葡聚糖得到了几种还原端为3,6-脱水-D-葡萄糖的寡糖。