An α-glucan was isolated from the culinary medicinal mushroom A. bisporus by hot water extraction, ethanol precipitation and DEAE-cellulose chromatography. The resulting material showed a single HMW peak excluded from a Sephadex G50 column that could completely be degraded by α-amylase treatment. After heating in 1% SDS a small additional peak of low MW eluted from the G50 column. The monosaccharide composition of the main peak was evaluated by HPLC, and was found to consist of a majority of glucose (97.6%), and a minor proportion of galactose (2.4%). Methylation analysis and degradation by α-amylase indicated the presence of an α-glucan with a main chain consisting of (1→4)-linked units, substituted at O-6 by α-D-glucopyranose single-units in the relation 1:8. Mono- ( 13C-, 1H-NMR) and bidimensional [1H (obs.),13C-HSQC] spectroscopy analysis confirmed the α-configuration of the Glcp residues by low frequency resonances of C-1 at δ 100.6, 100.2, and 98.8 ppm and H-1 high field ones at δ 5.06, 5.11, and 4.74 ppm. The DEPT-13C-NMR allowed assigning the non-substituted and Osubstituted -CH2 signals at δ 60.3/60.8 and 66.2 ppm, respectively. Other assignmentswere attributed to C-2, C-3, C-4, C-5 and C-6 of the non-reducing ends at δ 71.8; 72.8; 70.0; 71.3 and 60.3/60.8 ppm, respectively. The minor proportion of galactose that was demonstrated was probably derived from a complex between the α-glucan and a low molecular weight galactan.
NMR, polysaccharides, α-glucan, Basidiomycetes, medicinal mushrooms, Agaricus bisporus
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