Polysaccharides hydrolysis, acid

L (+) Arabmose is a naturally occurring L sugar It is obtained bj acid hydrolysis of the polysaccharide present in mesquite gum Write a Fischer pro ection for L (+) arabmose... 

D (+) Galactose is a constituent of numerous polysaccharides It is best obtained by acid hydrolysis of lactose (milk sugar) a disaccharide of d glucose and d galactose L (—) Galactose also occurs naturally and can be prepared by hydrolysis of flaxseed gum and agar The principal source of d (+) mannose is hydrolysis of the polysaccharide of the ivory nut a large nut like seed obtained from a South American palm... 

Abatzoglou, N. and Chornet, E. (1998) Acid hydrolysis of hemicellulose and cellulose. Theory and Applications, in Polysaccharides, Marcel Dekkes, New York, pp. 1007-1045. 

Rhamnogalacturonan 11 (RG-11) is a structurally complex, pectic polysaccharide that is present in the primary cell-walls of higher plants. It is composed of 60 glycosyl residues, and is a very complex molecule indeed. For example, on acid hydrolysis, at least ten different monosaccharides are formed, including the novel aceric acid (30), which is the only branched-... 

A structural study on lipid A and the O-specific polysaccharide of the lipopoly-saccharide from a clinical isolate of Bacteroides vulgatus from a patient with Crohn s disease was conducted by Hashimoto and coworkers [39]. They separated two potent virulence factors, capsular polysaccharide (CPS) and lipopolysaccharide (LPS), from a clinical isolate of B. vulgatus and characterized the structure of CPS. Next, they elucidated the strucmres of O-antigen polysaccharide (OPS) and lipid A in the LPS. LPS was subjected to weak acid hydrolysis to produce the lipid A fraction and polysaccharide fraction. Lipid A was isolated by PLC, and its structure was determined by MS and NMR. 

Although the glycosidic bonds of uronic acid residues are usually more resistant to acid hydrolysis than those of neutral polysaccharides,218 these linkages in heparin are more readily cleavable then those between the hexosamine and the uronic acid residues. Disaccharides obtained by exhaustive hydrolysis of heparin with 0.5 MHC1 at 80° contained hexu-... 

Acid hydrolysis of the polysaccharide portion of wood will release lignin but also causes major condensation reactions in the product(2l). These reactions can be minimized by using 41 wt. percent hydrochloric acid in place of other mineral acids but some condensation reactions still occur(22). This is not an effective method by which to obtain unaltered lignin. On the other hand, lignin can be solvent extracted from wood at temperature of 175°C using solvent mixtures such as 50/50 by volume water/1,4-dioxacyclohexane(23) Changes in lignin under these conditions appear to be minor. 

Pober, K.U., Hoff, M.H., and Darlington, R.K. "Water-Insoluble Residue Following Acid Hydrolysis of Water-Soluble Polysaccharides," J. Pet. Technol.(December 1983) 2185-2191. 

Gramnegative bacteria. The polysaccharide is determined as reducing substances after acid hydrolysis. Some polysaccharides yielded only one reducing sugar others yielded two or more sugars. 

We may return now to the polysaccharides present in the peanut for a brief consideration of the relationship of the other components present in the pectic materials to the araban constituent. All the evidence indicates that the pectic acid portion of the peanut is identical with normal pectic acid and, as was indicated in the previous section, this material, which is very stable to acid hydrolysis and possesses a high positive rotation contains a main chain which is built up of D-galac-turonic acid residues of the pyranose type. If, therefore, the araban associated with the pectic acid had been derived directly from the pectic acid by decarboxylation without intermediate hydrolysis of the poly-galacturonide, the sugar residues in the araban should also be in the pyranose form. The experimental evidence shows clearly, however, that the arabinose residues in araban are furanose in type and it follows that any hypothesis concerning the direct conversion of pectic acid into the araban by decarboxylation is untenable. 

Many plants store carbohydrates in their tubers in the form of polysaccharides which upon acid hydrolysis yield D-fructose as the main product. These polysaccharides differ from one another in the size of the molecule as well as in the position of the linkages between the D-fructose residues. Polyfructosans have also been prepared by enzymic action on sucrose. 

Acid hydrolysis of the basic hexasaccharide yielded the disaccharide 31. Its mobility in paper chromatography lay between those of the corresponding (1 — 3)-linked (from S10A) and /3-(l — 6)-linked (from S29) isomers, which is why it was assumed to be (1 — 4)-linked. The (1 — 2)-linked isomer was excluded, as the D-galactose residue that is part of 31 carries a D-galactopyranosyl group linked to 0-2 in the original polysaccharide, as will be discussed. 

Xylan has the general properties of insolubility in water, solubility in alkaline solutions, ease of acid hydrolysis, high negative optical rotation, and non-reducing action toward Fehling s solution. It can be placed in three general polysaccharide classes (1) pentosan, (2) glycan, and (3) hemicellulose. It is classed as a pentosan because it is principally a polymer of a pentose. It is by far the most abundant pentosan. 

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