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Holocellulose isolation

The investigations of Mitchell and Ritter - on holocellulose isolated from sugar maple are of interest. These workers isolated 25% of the holocellulose ill four, levorotatory, soluble fractions by successive treatments with hot water, cold 2% sodium carbonate, cold 4% sodium hydroxide, and hot 10% sodium hydroxide. The fraction extracted with hot water contained acetyl gi oups. All fractions contained xylan, and uronic anhydride and methoxyl were found in them in equivalent proportions. [Pg.320]

Relatively pure xylan isolated from the holocellulose of aspen (Populus) wood is said to contain 85% of xylose residues.78 One of the characteristic properties of xylan is its ease of hydrolysis. Because it hydrolyzes much more readily than cellulose, mild acid treatment may be employed to bring about preferential hydrolysis of xylan from plant material. Xylose is ordinarily prepared in the laboratory by direct sulfuric acid hydrolysis of the native xylan in ground corn cobs.74 Hydrolysis in hydrochloric acid proceeds rapidly, but decomposition to furfural also occurs to some extent.76 A commercial method for the production of D-xylose from cottonseed hulls76 and straw77 and from corn cobs17 78 has been described. [Pg.292]

Holocellulose Cellulosic material obtainable from wood after removal of lignin. The term therefore means total carbohydrates (cellulose and hemicellulose) present in the wood (Refs 1 2) Ritter (Ref 3) succeded in isolating holocellulose from wood pulp by repeated chlori-nations, followed by extraction with alcohol containing 3% of monoethanolamine. The resulting product was white but changed color on standing... [Pg.166]

Sprucewood holocellulose was treated with an endo-p-1,4-mannanase isolated from Aspergillus niger and an endo-/3-1,4-xylanase, two avicelases, and a cellobiohydrolase C isolated from Trichoderma viride. The mannanase hydrolyzed about a quarter of the mannan in 2-3 days without xylan or cellulose degradation. The xylanase hydrolyzed about half the xylan with 10% mannan solubilization. The three cellulases hydrolyzed up to 45% of the cellulose and 20% of the xylan, accompanied by 40-70% solubilization of the mannan. Combined xylanase-mannanase treatment hydrolyzed about half the xylan and mannan. Addition of mannanase to to cellulose-treated samples increased the degradation of the cellulose and mannan. Micromorphological studies of the variously treated specimens revealed a loss of substances in P/Slf T, and adjacent zones of S2 of the tracheid wall. [Pg.301]

The xylanase hydrolyzed about half the xylan in the sprucewood holocellulose. This is in the range of the xylan degradation obtained in former studies with delignified beechwood (7,10,22). Boutelje et al. (5) reported only 20-30% xylan hydrolysis of sprucewood holocellulose by a xylanase, even after repeated treatments. They used the same holocellulose and a xylanase isolated from the same commercial enzyme preparation as were used in the mannanase treatment referred to above. The holocellulose contained only a low xylan portion and very little arabinose this could be the reason for the inferior degradation rate, and hence it is not surprising that no free arabinose was detected, in contrast to what... [Pg.321]

The three cellulases decomposed about 25-45% of the cellulose accompanied by solubilization of about 40-70% of the mannan and, by partial hydrolysis, of about 20% of the xylan present in the untreated sprucewood holocellulose. Based on the degradation products (cf. Table III, Columns 13-15, and Table II), the catalytic actions of the three cellulases—all isolated from Trichoderma viride—are similar or identical. The lower absolute degradation values obtained with cellobiohydrolase C might merely be a result of enzyme concentration. [Pg.322]

The catalytic action of the two avicelases and the cellobiohydrolase C seems at least to be different from those of the xylanases isolated from Trichoderma viride i.e., the degradation products have a higher degree of polymerization even after prolonged incubation and, in the case of sprucewood holocellulose, no arabinose is liberated. [Pg.323]

Woods contain a number of acyl (mainly acetyl) groups, and it is probable that these are associated with the xylan components of the hemicellulose fraction. Evidence for the original esterification of aspen-wood xylan comes from the observation that the isolated xylan (obtained by alkaline extraction) is readily cleaved by periodate, whereas only a small proportion of the D-xylose residues in the wood itself are oxidized under similar conditions.66 Hemicelluloses still containing acyl groups may be extracted from wood holocelluloses by means of dimethyl sulfoxide, and further quantities... [Pg.462]

Holocellulose was isolated from bamboo powders by removing lignin and resinous compounds using alternate treatments of glacial acetic acid and sodium chlorite at 70-80 C for three hours according to the method of Ku and Chiou (20). [Pg.234]

The only pentosans which have been studied to any great extent are the xylans. These can be obtained from all lignified cell membranes by extraction with 5% sodium hydroxide solution after lipids, pectic materials etc. have been removed. The conditions necessary to avoid degradation during isolation have been outlined.2 Early structural determinations indicated that arabinose was present as a non-reducing end-group in a branched molecule which had a chain-length of 18-20 D-xylo-furanose residues.27 It has been shown recently, however, that the xylan from esparto holocellulose can be purified free of arabinose after several re-precipitations of the copper-complex.28... [Pg.299]

Hemicellulose Samples. Two water-soluble hemicellulosic samples were used (1) acetyl-4-O-methylglucuronoxylan (molecular weight = 30,000) from white birchwood, isolated by the extraction of chlorine holocellulose with dimethyl sulfoxide and (2) arabinogalactan, Stractan from St. Regis Paper Company (arabinose galactose = 1 6 molecular weight = 60,000), prepared by the water extraction of heartwood of western larch. Both samples were kindly provided by T. E. Timell (SUNY). [Pg.369]

Another method of isolating holocellulose from wood and similar lignified tissues by the use of sodium chlorite and acetic acid was devised by Jayme and modified by Wise, Murphy and D Addieco. The latter... [Pg.188]

A new approach to the isolation of hemicelluloses is through the production of holocellulose by chlorination of the wood followed by extraction of the holocellulose with a 3% solution of ethanolamine in alcohol. The holocellulose contains the carbohydrate portion of the wood freed of lignin. Hemicelluloses are then extracted from this product in the regular way. " ... [Pg.333]

The wastes were milled and screen-sieved. Wastes composition was determined in terms of the major constituent biopolymers, holocellulose (cellulose + hemicellulose) and lignin, and extractive components that are soluble in ethanol-benzene. Lignin and extractives were isolated according to TAPPI standard methods. Holocellulose was obtained following the procedure described elsewhere (9). [Pg.1117]

IR spectroscopic evidence for covalent urethane bond formation in the reaction between isocyanates and wood has been obtained. Isolation of holocellulose by the sodium chlorite method, isolation of lignin by the H2SO4 procedure, and subjecting both to IR spectroscopy indicated that isocyanates reacted with both cellulose and lignin (194),... [Pg.392]


See other pages where Holocellulose isolation is mentioned: [Pg.317]    [Pg.317]    [Pg.26]    [Pg.27]    [Pg.53]    [Pg.88]    [Pg.620]    [Pg.302]    [Pg.320]    [Pg.321]    [Pg.322]    [Pg.453]    [Pg.462]    [Pg.463]    [Pg.64]    [Pg.295]    [Pg.303]    [Pg.313]    [Pg.319]    [Pg.202]    [Pg.1491]    [Pg.292]    [Pg.292]    [Pg.268]    [Pg.276]    [Pg.277]    [Pg.257]    [Pg.257]    [Pg.258]    [Pg.260]    [Pg.261]    [Pg.261]    [Pg.262]   
See also in sourсe #XX -- [ Pg.317 ]




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