Table 3.
Method | Information | Characteristic | References |
---|---|---|---|
Partial acid hydrolysis | Ranking of stability of various sugar: the pyran sugar residue>the furan sugar residue, the hexose sugar>the pentose sugar, the sugar residues in main chain>the branched sugar residues | Poor selectivity, requires precise reaction conditions, not suitable for the complex mixed polysaccharides or heterogeneous structure products | (88–90) |
Periodic acid oxidation | The position of glycosidic bonds; the degree of polymerization of linear polysaccharides; the number of branches of branched polysaccharides. | Carried out in the dark in an aqueous solution with pH 3–5, less polysaccharide samples are required | (4) |
Smith degradation | Degradation product erythrose: 1 → 4 combined glycosidic bonds; glycerol:1 → 6, 1 → 2 glycosidic bonds or a reducing terminal glucose residue; monosaccharides such as glucose, galactose, mannose: 1 → 3 glycosidic bonds. | Combined with periodic acid oxidation | (91) |
Methylation reaction | GC/MS spectral library; the standard PMAA spectrum; the ionization law of PMAA. |
α/β stereochemical information cannot be obtained | (92, 93) |
Enzymatic digestion | α-glucosidase hydrolysis α-glycosidic bond; β-glucosidase hydrolysis β-glycosidic bond. | Specific, few by-products, little digestive enzymes for polysaccharide | (94, 95) |