N. Nakajima et al., Multi-enzymatic glucosylation using Eucalyptus UDP-glucosyltransferase coupled UDPglucose-fermentation by bakers' yeast, BIOS BIOT B, 63(5), 1999, pp. 934-936
The enzymatic synthesis of glucoside compounds using a membrane-associated
UDP-glucosyltransferase fraction from Eucalyptus perriniana cultured cells
as a water-insoluble catalyst (N. Nakajima, et. at., J. Ferment. Bioeng., 8
4 (5), pp. 455-460, 1997) has been effectively done by coupling UDPglucose-
fermentation by bakers' yeast. For example, beta-thujaplicin (hinokitiol) a
nd p-aminobenzoic acid were converted respectively to their corresponding b
eta-D-monoglucosides with the conversion rate of around 24-26% by the multi
-enzymatic system with UDPglucose as a glucose donor, which is produced by
yeast cells from glucose and 5'-UMP. Addition of either cellobiose, a subst
rate of beta-glucosidase, or DL-1,2-anhydro-myo-inositol, an inhibitor for
the enzyme in the reaction mixture, could increased the yield of these beta
-D-monoglucosides. This new enzymatic system could also be used for the syn
thesis of flavonoid glucosides such as isoquercitrin (quercetin 3-O-beta-D-
glucoside).