| Literature DB >> 27832720 |
Yuta Sugiyama1, Toshihiko Katoh1,2, Yuji Honda1, Aina Gotoh1,2, Hisashi Ashida3, Shin Kurihara1, Kenji Yamamoto1, Takane Katayama1,2.
Abstract
We have recently generated a highly efficient 1,2-α-l-fucosynthase (BbAfcA N423H mutant) by protein engineering of 1,2-α-l-fucosidase from Bifidobacterium bifidum JCM 1254. This synthase could specifically introduce H-antigens (Fucα1-2Gal) into the non-reducing ends of oligosaccharides and in O-linked glycans in mucin glycoprotein. In the present study, we show an extended application of the engineered 1,2-α-l-fucosynthase by demonstrating its ability to insert Fuc residues into N- and O-glycans in fetuin glycoproteins, GM1 ganglioside, and a plant-derived xyloglucan nonasaccharide. This application study broadens the feasibility of this novel H-antigen synthesis technique in functional glycomics.Entities:
Keywords: 1,2-α-l-fucosidase; H-antigen; glycosynthase; oligosaccharide; sugar chains
Mesh:
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Year: 2016 PMID: 27832720 DOI: 10.1080/09168451.2016.1254532
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043