| 摘要 |
In the present invention, O-arylalpha-glycoside is synthesized in excellent efficiency by using an enzymatic synthesis method by reacting glycosyl donor and carbohydrate receptor under the existence of acid/base catalyst residues changed into inactivated amino acid residues and alpha-thioglycoligase which is a mutant of alpha-glycosidase or alpha-xylosidase. |
