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Endo‐α‐Mannosidase‐Catalyzed Transglycosylation
Authors:Shogo Iwamoto  Yuta Kasahara  Prof?Dr Yayoi Yoshimura  Dr Akira Seko  Prof?Dr Yoichi Takeda  Prof?Dr Yukishige Ito  Prof?Dr Kiichiro Totani  Prof?Dr Ichiro Matsuo
Affiliation:1. Graduate School of Science and Technology, Gunma University, Kiryu, Gunma, Japan;2. ERATO Science and Technology Agency, JST), Ito Glycotrilogy Project, Wako, Saitama, Japan;3. Department of Biotechnology, Ritsumeikan University, Shiga, Japan;4. Synthetic Cellular Chemistry Laboratory, RIKEN, Wako, Saitama, Japan;5. Department of Materials and Life Science, Seikei University, Musashino, Tokyo, Japan
Abstract:In order for facilitating the synthesis of oligosaccharides, transglycosylation reactions mediated by glycoside hydrolases have been studied in various contexts. In this study, we examined the transglycosylating activity of a Golgi endo ‐ α‐mannosidase. We prepared various glycosyl donors and acceptors, and recombinant human Golgi endo‐α‐mannosidase and its various mutants were expressed. The enzyme was able to mediate transglycosylation from α‐glycosyl‐fluorides. Systematic screening of various point mutants revealed that the E407D mutant had excellent transglycosylation activity and extremely low hydrolytic activity. Substrate specificity analysis revealed that minimum motif required for glycosyl acceptor is Manα1– 2Man. The synthetic utility of the enzyme was demonstrated by generation of a high‐mannose‐type undecasaccharide (Glc1Man9GlcNAc2).
Keywords:enzymes  glycosylation  glycosynthases  oligosaccharides  transglycosylation
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