Xylan acidic

Xyhtol is synthesized by reduction of D-xylose catalyticahy (40), electrolyticahy (41), and by sodium amalgam (42). D-Xylose is obtained by hydrolysis of xylan and other hemiceUulosic substances obtained from such sources as wood, com cobs (43), almond shells, hazelnuts, or oHve waste (44). Isolation of xylose is not necessary xyhtol results from hydrogenation of the solution obtained by acid hydrolysis of cottonseed hulls (45). 

The L-arabino-(4-0-methyl-D-glucurono)xylans are found in softwoods and annual plants. The L-arabinose is present primarily as a-L-arabinofuranosyl units, although P-L-arabinopyranosyl units may also be present. In either case, the arabinosyl units are often, but not always, present as single-unit side chains, as are the uronic acid units. 

P -D-xylan with 3-hnked a-L-arabiaose branches (1 4)-P -D-xylan with 2-Unked 4-0-methyl-a-D-glucuronic acid and arabiaose branches... 

Most of the glucuronoxylans have single 4-0-methyl-o -D-glucopyranosyl uronic acid residues (MeGlcA) attached always at position 2 of the main chain Xylp units (Fig. 2). This structural type is usually named as 4-0-methyl-D-glucurono-D-xylan (MGX). However, the glucuronic acid side chain may be present in both the 4-0-methylated and non-methylated forms (GlcA). 

The heteroxylans (CHX) present in cereals, seeds, gum exudates, and mucilages are structurally more complex [6]. They have a (1 4)-)0-d-xylopyranose backbone decorated, except of the single uronic acid and arabinosyl residues with various mono- and oligoglycosyl side chains. Reinvestigations of CHX isolated from corn bran [52] have confirmed that the xylan backbone is heavily substituted (at both positions 2 and 3) with y0-D-Xylp, y0-L-Ara/, of-D-GlcpA residues and oligosaccharide side chains (1), (3) and (4). 

The foamability of the xylans tested [128] was low in comparison to a commercial whipping protein DIOO. Only the highly viscous beech wood xylan and the rye bran AX-protein complex exhibited remarkable foaming activity, which was similar to that of gum arable. As the MGX polymers contain considerable amounts of uronic acid side chains, this may play a role in their foaming activity together with the presence of low amounts of Ugnin. 

Xylan sulphates, known also as pentosan polysulphates (PPS), are permanently studied with regard to their biological activities [3,419-422]. Usually, sulphuric acid, sulphur trioxide, or chlorsulphonic acid are employed as sul-phating agents alone or in combination with alcohols, amines or chlorinated hydrocarbons as reaction media [423]. 

Xylan-based micro- and nanoparticles have been produced by simple coacervation (Garcia et al., 2001). In the study, sodium hydroxide and chloride acid or acetic acid were used as solvent and non-solvent, respectively. Also, xylan and surfactant concentrations and the molar ratio between sodium hydroxide and chloride acid were observed as parameters for the formation of micro- and nanoparticles by the simple coacervation technique (Garcia et al., 2001). Different xylan concentrations allowed the formation of micro- and nanoparticles. More precisely, microparticles were found for higher concentrations of xylan while nanopartides were produced for lower concentrations of the polymer solution. When the molar ratio between sodium hydroxide and chloride acid was greater than 1 1, the partides settled more rapidly at pH=7.0. Regarding the surfactant variations, an optimal concentration was found however, at higher ones a supernatant layer was observed after 30 days (Garda et al., 2001). 

The floss silk from Chorisia speciosa furnished a polysaccharide with a main chain of (1 -> 4) linked P-Xylp substituted at 0-2 by 5 % of uronic acid. The xylan structure also was interposed with a-Rhap units in small amounts. The defatted seeds furnished on aqueous extraction a major fraction, ((9-acetyl, 10 % and protein, 45 %) wich was hydrolysed and analysed by p.c. and GLC, showing Rha (20 %), Ara (16 %), Gal (64 %) and also uronic acids (45 %). Partial hydrolysis gave rise to a polysaccharide free of arabinose, with 46 % of uronic acids. Methylation analysis (GLC -MS) indicated a chain of (1 4) - linked Gal/ (42 % of 2,3,6-Me3-Gal). 

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