Characterization of polysaccharides from cystocarpic and tetrasporic stages of Sub - Antarctic Iridaea cordata
The polysaccharide systems from cystocarpic and tetrasporic phases of the Sub-Antarctic algae Iridaea cordata were studied. Cystocarpic plant polysaccharides are mainly composed by carrageenans of the κ–family. However, agaran structures were also detected in the fraction soluble in 2.00 M KCl, after fractionation with increasing potassium chloride solutions. The presence of B-D-galactose-α-L-galactose 3-sulfate, B-D-galactose-a-L-galactose 6- sufate, B-D-galactose 6-sulfate-α-L-galactose 6-sufate, and of B-D-galactose 4-sulfate-a-L-galactose 2,3-disulfate diads was confirmed by means of methylation and NMR spectroscopy analyses; the latter diad has been scarcely reported. The first extracts from tetrasporic plants rendered a pure λ-carrageenan with considerable yield, which confers this species promising commercial applications. In some cystocarpic and tetrasporic extracts a-glucose was also found and assigned to floridean starch by 1 H-13C HSQC NMR spectroscopy.
| Summary: | The polysaccharide systems from cystocarpic and tetrasporic phases of the Sub-Antarctic algae Iridaea cordata were studied. Cystocarpic plant polysaccharides are mainly composed by carrageenans of the κ–family. However, agaran structures were also detected in the fraction soluble in 2.00 M KCl, after fractionation with increasing potassium chloride solutions. The presence of B-D-galactose-α-L-galactose 3-sulfate, B-D-galactose-a-L-galactose 6- sufate, B-D-galactose 6-sulfate-α-L-galactose 6-sufate, and of B-D-galactose 4-sulfate-a-L-galactose 2,3-disulfate diads was confirmed by means of methylation and NMR spectroscopy analyses; the latter diad has been scarcely reported. The first extracts from tetrasporic plants rendered a pure λ-carrageenan with considerable yield, which confers this species promising commercial applications. In some cystocarpic and tetrasporic extracts a-glucose was also found and assigned to floridean starch by 1 H-13C HSQC NMR spectroscopy. |
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