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Novel enzymatic approach to the synthesis of flavonoid glycosides and their esters
Author(s) -
Gao Chunli,
Mayon Patrick,
MacManus David A.,
Vulfson Evgeny N.
Publication year - 2000
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/1097-0290(2000)71:3<235::aid-bit1013>3.0.co;2-m
Subject(s) - glycoside , flavonoid , chemistry , enzyme , organic chemistry , biochemistry , stereochemistry , antioxidant
Flavonoids such as (+)catechin can be efficiently solubilised in supersaturated solutions prepared with donor glycosides, e.g., p ‐nitrophenyl glycosides, di‐ and higher oligosaccharides, and poly(ethylene glycol) dimethyl ether in sufficiently high concentration for their efficient enzymatic glycosylation. Under these conditions several glycosidases readily accept (+)catechin as substrate and the target glycosides were prepared in one step in up to 26% yields. The regioselectivity of the reaction depends on the enzyme and substrate combination used; three positions, 5, 7, and 4′, in the flavonoid can be glycosylated. The resulting and similar flavonoid glycosides were further modified by regioselective acylation with vinyl esters of arylpropenoic acids using lipases as biocatalyst. The efficiency of acylation was found to diminish in the order of vinyl cinnamate > vinyl ferulate > vinyl coumarate. This work demonstrates the feasibility of assembling complex flavonoid glycoside esters in just two steps by sequential use of commercially available glycosidases and lipases. © 2001 John Wiley & Sons, Inc. Biotechnol Bioeng 71: 235–243, 2000/2001.