The structure of sulfated oligosaccharide II, one of the main sulfated oligosaccharide chains of ovomucin, has been determined. This oligosaccharide was found to compose of each 1 mole of N-acetylgalactosaminitol, galactose, N-acetylneuraminic acid and sulfate. The sequential periodate oxidation, borohydride reduction and acid hydrolysis of N-acetylneuraminic acid-free oligosaccharide resulted in the formation of glycerol and N-acetylthreosaminitol. From these results, the following structure was proposed for sulfated oligosaccharide II: N-acetylneuraminyl-(2→3)-galactosyl-(1→3)-N-acetylgalactosaminitol-6-sulfate.
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Kato et al. (1978) studied this question.