PubMed:8156559 / 292-295
|
NMR spectroscopic investigation of agarose oligomers produced by an alpha-agarase.
The 13C NMR signals of various even and odd agarose oligosaccharides with either D-galactose or 3,6-anhydro-alpha-L-galactose at the reducing end have been assigned. The chemical shifts in water of the agaro- and the neoagaro-oligosaccharides are compared and the influence of dimethyl sulfoxide on the chemical structure of the agaro-oligosaccharides is reported. The 3,6-anhydro-L-galactose residue at the reducing end of agaro-oligosaccharides is in the hydrated form.
|
Annnotations
- Denotations: 1
- Blocks: 0
- Relations: 0