Characterization of acetylated 4-O-methylglucuronoxylan isolated from aspen employing 1H and 13C NMR spectroscopy
2000
Abstract Water-soluble hemicelluloses were extracted from milled aspen wood ( Populus tremula ) employing microwave oven treatment at 180 °C for 10 min. The final pH of this extract was 3.5. From this extract oligo- and polysaccharides were isolated and subsequently fractionated by size-exclusion chromatography. The structures of the saccharides in three of the fractions obtained were determined by 1 H and 13 C NMR spectroscopy, using homonuclear and heteronuclear two-dimensional techniques. The polysaccharides present in the two fractions eluted first were O -acetyl-(4- O -methylglucurono)xylans. The average degree of acetylation of the xylose residues in these compounds was 0.6. The structural element →4)[4- O -Me-α- d -Glc p A-(1→2)][3- O -Ac]-β- d -Xyl p -(1→ could also be identified. On the average, these two xylans were composed of the following (1→4)-linked β- d -xylopyranosyl structural elements: unsubstituted (50 mol%), 2-O-acetylated (13 mol%), 3-O-acetylated (21 mol%), 2,3-di-O-acetylated (6 mol%) and [MeGlcA α-(1→2)][3-O-acetylated] (10 mol%). Most of the 4- O -methylglucuronyl and acetyl substituents in the isolated polysaccharides survived the microwave oven treatment. The third fraction, eluted last, contained acetylated xylo -oligosaccharides, with minor contamination by an acetylated mannan. In the case of these xylo -oligosaccharides, the average degree of acetylation was 0.3.
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