A Chemoenzymatic Route to Conjugatable β(1→3)-Glucan Oligosaccharides
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.
1992 ◽
Vol 50
(1)
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pp. 844-845
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2016 ◽
Vol 51
(3)
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pp. 335-342
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Keyword(s):
2017 ◽
Vol 20
(4)
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Keyword(s):
2008 ◽
2019 ◽
pp. 140-150
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