Galβ1Ǟ4 disaccharide structures are vital core units of the rides {Galβ1Ǟ4GlcNAcαOAll (3), Galβ1Ǟ4GlcNAcβOAll (5), Galβ1Ǟ4GalαOAll (10), Galβ1Ǟ4GalβOAll (12), Galβ1Ǟ oligosaccharide components of glycoconjugates. β-Galactosidase from Bacillus circulans (E.C.3.2.1.23) catalyses the transfer 4GalβSPh
Regioselective Synthesis of Galactosylated Tri- and Tetrasaccharides by Use of β-Galactosidase from Bacillus circulans.
✍ Scribed by Erzsebet Farkas; Ulja Schmidt; Joachim Thiem; Joerg Kowalczyk; Markwart Kunz; Manfred Vogel
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 58 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
The aim of this research is to develop a model to describe oligosaccharide synthesis and simultaneously lactose hydrolysis. Model A (engineering approach) and model B (biochemical approach) were used to describe the data obtained in batch experiments with -galactosidase from Bacillus circulans at v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract The enzymatic synthesis of N‐acetyl‐lactosamine (LacNAc) by the transgalactosylation of N‐acetyl‐D‐glucosamine (GlcNAc), catalyzed by the β‐galactosidase from Bacillus circulans (BcβGal), was studied in hydro‐organic media, starting from o‐nitrophenyl‐β‐D‐galactopyranoside (oNPG) as a g
## Abstract The enzymatic synthesis of __N__‐acetyl‐lactosamine (LacNAc) was studied in aqueous media with high substrate concentrations using the transgalactosylation of __N__‐acetyl‐D‐glucosamine (GlcNAc), starting from lactose as a galactosyl donor. The efficiency and regioselectivity of the β‐g