REGIOSELECTIVITY OF THE ENZYMATIC TRANSGALACTOSIDATION OF D-XYLOSE AND L-XYLOSE CATALYZED BY BETA-GALACTOSIDASES

Citation
E. Montero et al., REGIOSELECTIVITY OF THE ENZYMATIC TRANSGALACTOSIDATION OF D-XYLOSE AND L-XYLOSE CATALYZED BY BETA-GALACTOSIDASES, Carbohydrate research, 305(3-4), 1997, pp. 383-391
Citations number
27
Categorie Soggetti
Chemistry Applied","Chemistry Inorganic & Nuclear",Biology
Journal title
ISSN journal
00086215
Volume
305
Issue
3-4
Year of publication
1997
Pages
383 - 391
Database
ISI
SICI code
0008-6215(1997)305:3-4<383:ROTETO>2.0.ZU;2-5
Abstract
The regioselectivity of enzymatic transgalactosidation depends on the source of the beta-galactosidase used. When the galactosyl acceptor on ly contains secondary hydroxyl groups, of anp of the three regioisomer s 4-, 3- and 2-O-beta-D-galactopyranosyl-D-xylose (1, 2 and 3, respect ively) or 4-, 3-and 2-O-beta-D-galactopyranosyl-L-xylose (4, 5 and 6, respectively). Enriched mixtures in 1, 2 or 3 were obtained using beta -galactosidases from Escherichia coli, bovine testes or Aspergillus or yzae, respectively, by transgalactosidation reaction of O-nitrophenyl- beta-D-galactopyranoside and D-xylose, and enriched mixtures in 4, 5 o r 6 were obtained in a similar way using beta-galactosidases from Aspe rgillus oryzae, lamb small-intestine (intestinal lactase-phloridzin hy drolase) or Saccharomyces fragilis, respectively, using L-xylose as ac ceptor. (C) 1998 Elsevier Science Ltd.