期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 11, 期 18, 页码 2503-2506出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(01)00474-7
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The alpha -Gal trisaccharide Gal alpha (1 -->3)Gal beta (1 -->4)GlcNAc 11 was synthesized on a homogeneously soluble polymeric support (polyethylene glycol, PEG) by use of a multi-enzyme system consisting of beta -1,4-galactosyltransferase (EC 2.4.1.38), alpha -1,3-galactosyltransferase (EC 2.4.1.151), sucrose synthase (EC 2.4.1.13) and UDP-glucose-4-epimerase (EC 5.1.3.2). In addition workup was simplified by use of dia-ultrafiltration. Thus the advantages of classic chemistry/enzymology and solid-phase synthesis could be united in one. Subsequent hydrogenolytic cleavage afforded the free alpha -Gal trisaccharide. (C) 2001 Elsevier Science Ltd. All rights reserved.
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