PubMed:8156559
Annnotations
{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/8156559","sourcedb":"PubMed","sourceid":"8156559","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/8156559","text":"NMR spectroscopic investigation of agarose oligomers produced by an alpha-agarase.\nThe 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 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