Abstract
The use of biocatalysts from yeast strains in organic synthesis is well established and covers a broad range of reaction classes. A particularly interesting reaction class is the regio- and stereospecific attachment of sugar moieties (i.e. glycosylation) to a variety of natural
products, from small molecules up to oligosaccharides and proteins. Since the bioactivity of many therapeutics depends on the proper glycosylation, the improvement of glycosylation methodology by chemical synthesis, biocatalysis or in vivo approaches is of major interest. We have developed
glycosyltransferase-toolkits for the straight-forward and quantitative transfer of a specific monosaccharide moiety to an acceptor substrate. The stable expression of the ?(1?4)-galactosyltransferase I in Saccharomyces cerevisiae and ?(1?3)-fucosyltransferase VI
in Pichia pastoris has enabled these biocatalysts to be prepared in large-scale for use in organic synthesis. The application of galactosyltransferase using UDP-galactose and fucosyltransferase using GDP-fucose as NDP-sugar donor in the regio- and stereospecific galactosylation and
fucosylation of small molecules is shown with a simplified reaction system. Optimisation of the reaction conditions allows for quantitative glycosylation reactions. The use of recombinant yeasts has been the key to performing this highly efficient glycosylation methodology and represents a
building block of biocatalytic glycomics for the future.
Subject
General Medicine,General Chemistry
Cited by
11 articles.
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