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Type: Journal article
Title: A chemoenzymatic route to conjugatable beta(1 -> 3)-glucan oligosaccharides
Author: Montel, E.
Hrmova, M.
Fincher, G.
Driguez, H.
Cottaz, S.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 2009; 62(6):575-584
Publisher: C S I R O Publishing
Issue Date: 2009
ISSN: 0004-9425
Statement of
Emilie Montel, Maria Hrmova, Geoffrey B. Fincher, Hugues Driguez and Sylvain Cottaz
Abstract: 3II-O-Allyl-α-laminaribiosyl fluoride was prepared as a key synthon for the enzymatic synthesis of β(1→3)-glucan oligosaccharides, catalyzed by a mutated β(1→3)-glucanase (E231G) from barley (Hordeum vulgare L.). A strategy was developed for enzymatic elongation of the β(1→3)-glucan chain from the reducing end, using a single glucoside acceptor. When β-glucoside phenyl disulfide was used as the acceptor, this methodology generated laminari-oligosaccharides conjugatable at both their reducing and non-reducing ends.
DOI: 10.1071/CH08517
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