| Literature DB >> 12054949 |
Jakob F Tolborg1, Lars Petersen, Knud J Jensen, Christoph Mayer, David L Jakeman, R Antony J Warren, Stephen G Withers.
Abstract
Enzymatic approaches for the preparation of oligosaccharides are interesting alternatives to traditional chemical synthesis, the main advantage being the regio- and stereoselectivity offered without the need for protecting groups. The use of solid-phase techniques offers easy workup procedures and the prospect of automatability. Here, we report the first application of glycosynthases to solid-phase oligosaccharide synthesis by use of the 51 kDa serine and glycine mutants of Agrobacterium sp. beta-glucosidase, Abg E358S and E358G. Acceptors were linked to PEGA resin through a backbone amide linker (BAL), and using these mutated enzymes, a galactose moiety was transferred from a donor sugar, alpha-D-galactosyl fluoride, with high efficiency (>90%) together with excellent recovery of material. Furthermore, it was demonstrated that a resin-bound model glycopeptide was also an acceptor for the glycosynthase.Entities:
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Year: 2002 PMID: 12054949 DOI: 10.1021/jo0163445
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354