ENZYMATIC-SYNTHESIS OF ALPHA-LINKED GALACTOOLIGOSACCHARIDES USING THEREVERSE REACTION OF A CELL-BOUND ALPHA-GALACTOSIDASE FROM CANDIDA-GUILLIERMONDII H-404
H. Hashimoto et al., ENZYMATIC-SYNTHESIS OF ALPHA-LINKED GALACTOOLIGOSACCHARIDES USING THEREVERSE REACTION OF A CELL-BOUND ALPHA-GALACTOSIDASE FROM CANDIDA-GUILLIERMONDII H-404, Bioscience, biotechnology, and biochemistry, 59(2), 1995, pp. 179-183
alpha-Linked galactooligosaccharides (alpha-GOS A from galactose, and
alpha-GOS B from lactose hydrolyzates) were synthesized using the reve
rse reaction of a-galactosidase from Candida guilliermondii H-404. The
alpha-GOS A and B were isolated and their structures were identified
by methylation analysis. The main product of the disaccharides in alph
a-GOS A and alpha-GOS B was the (1,6)-isomer. The remaining disacchari
des consisted of (1,3)-, (1,2)-, and (1,1)-isomers. Conditions for syn
thesis of alpha-GOS B from lactose hydrolyzates were examined, The yie
ld of alpha-GOS B was approximately 20% when the mixture of heat-treat
ed cells containing alpha-galactosidase (60 U/g galactose) and 85% lac
tose hydrolyzates was incubated for 90 h at pH 4.5 and 50 degrees C. T
he alpha-GOS A and B were available as the donor substrates in transga
lactosylation of alpha-galactosidase in the same manner as melibiose.