Structure determination of galacto-oligosaccharides by pyridylamination and NMR spectroscopy
✍ Scribed by Kazumasa Kimura; Keisuke Matsumoto; Chiyoko Ishihara; Katsuhisa Harada; Akihiko Miyagi
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 487 KB
- Volume
- 270
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
Galacto-oligosaccharides formed from lactose by the action of some /3-galactosidases were subjected to gel chromatography on Bio-Gel P-2, and the resulting oligosaccharide fractions were converted into pyridylamino (PA) derivatives. Each PA-oligosaccharide fraction, which consisted of several isomers in a given size-class, was then subjected to HPLC on an ODS column. Twenty-one individual galacto-oligosaccharide components were isolated in this way. The structures of most of these compounds, namely six disaccharides, five trisaccharides, two tetrasaccharides, and a pentasaccharide, were determined by 13C-NMR spectroscopy. The results obtained will be useful for the study of the activity of various galacto-oligosaccharides on the growth of Bifidobacterium species.
📜 SIMILAR VOLUMES
1D NMR ('H and 13C) and 2D NMR spectroscopy have been used to determine the structure of feruloylated oligosaccharides obtained by enzymic degradation or mild acid hydrolysis of sugar-beet pulp. Feruloylated oligosaccharides derived from pectic neutral side-chains containing arabinose or galactose r
## The investigation of the chemical constituents of Symplocos racemosa Roxb led to the isolation of two new glycosides, symcomoside A (1) and symcomoside B (2), together with one known glycoside, tortoside C (3), which is reported for the first time from this plant. The structures of the new comp
## Abstract Ramosine, a new sesquiterpene lactone, was isolated from the chloroform fraction of __Amberboa ramosa__ and the structure was assigned as 4β‐(hydroxymethyl)‐3β,4α‐dihydroxy‐8α‐[(__S__)‐3‐hydroxy‐2‐ethylenepropionyloxy]‐1αH, 5αH,6βH,7αH,11βH,11α‐methylguaia‐10(14)‐en‐6, 12‐olide by exten
Two isomers of betamethasone 9a-fluoro-11~,17a,21-trihydroxy-l6~-methy~pregna-l,4diene-3,2~ione (l), were isolated from the mother liquor of a manufacturing process and were characterized by NMR spectroscopy. They were identified as 8a-fluoro-l1~,17a,2l-trihydroxy-l6~-methyl-9~-pregna-l,4-diene-3,20
Homologous series of dihydroxamic acids [HONHCO(CH 2 n CONHOH with n D 0, 1, 2, 3, 4 and 6] were prepared and trimethysilylated [1(n) and 2(n)]. The solution NMR spectra ( 1 H, 13 C, 15 N) of 1(n) show that the hydroxamic end groups assume Z-Z and Z-E combinations of conformers. An exception is oxal