Abstract
A mixture of oligosaccharides produced by β-galactosidase using lactose as a substrate was fractionated according to degree of polymerization using gel filtration, followed by high-pH anion-exchange chromatography. The fractions obtained were analyzed using monosaccharide analysis, methylation analysis, mass spectrometry, and NMR spectroscopy. Twelve novel non-reducing oligosaccharides were characterized, namely, [β-D-Galp-(1→4)](n)-α-D-Glcp-(1⇆1)-β-D-Galp[-(4←1)-β-D-Galp](m), with n, m=(1, 2, 3, or 4) and β-D-Galp-(1→2)-α-D-Glcp-(1⇆1)-β-D-Galp. Copyright (C) 1998 Elsevier Science Ltd.
| Original language | English |
|---|---|
| Pages (from-to) | 101-114 |
| Number of pages | 14 |
| Journal | Carbohydrate Research |
| Volume | 314 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 21 Dec 1998 |
Keywords
- β-Galactosidase
- Functional food
- Non-reducing galacto-oligosaccharides
- Oligogalactosylated glucoses
- Primary structure analysis
- Transgalactosylation
- beta galactosidase
- lactose
- oligosaccharide
- anion exchange chromatography
- article
- carbohydrate analysis
- carbohydrate synthesis
- chemical modification
- gel filtration chromatography
- mass spectrometry
- methylation
- nuclear magnetic resonance spectroscopy
- polymerization
- priority journal
- reaction analysis
Fingerprint
Dive into the research topics of 'α-D-Glcp-(1⇆1)-β-D-Galp-containing oligosaccharides, novel products from lactose by the action of β-galactosidase'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver