Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Monosaccharides from hemicellulose

Complete utilization of cellulose and hemicellulose requires selection or genetic modification of an organism that is able to ferment pentoses. In order to obtain monosaccharides from the raw material, several pretreatments and/or separations are required. First, the lignocellulosic material is mechanically treated and then delignified (pulped) by strong alkali or acid treatment. The (hemi)cellulose part becomes more accessible for enzymes at the same time. Subsequent enzymatic treatment mainly yields glucose and xylose and some arabinose. The enzymatic treatment and subsequent fermentation can be done in separate reactors or in one fermenter, in an SSF concept similar to starch SSF [57]. [Pg.12]

Wood chips can also be utilized as such to produce bioethanol. The cellulose and hemicellulose material is hydrolyzed in the presence of acids (H2SO4, HCl, or HCOOH) or enzymes to yield glucose and other monosaccharides [16]. Lignin is separated by filtration as a solid residue and the monosaccharides are fermented to ethanol, which, in turn, is separated from water and catalyst by distillation. Ethanol can be used not only as energy source but also as a platform component to make various chemicals, such as ethene and polyethene. Today green acetaldehyde and acetic acid from wood-derived bioethanol is manufactured by SEKAB Ab, at the Ornskoldsvik Biorefinery of the Future industrial park. [Pg.166]

Rha, Ara and Gal are the neutral sugar components from all the fractions. Xyl is not present in Fla and is significantly present in the hemicellulose fractions, indicating that this monosaccharide is component of hemicellulosic polymers. Chemical composition of the water fractions were determined (Table V). High protein contents and the presence of O-acetyl-groups were observed in four aqueous fractions. Neutral sugar and uronic acid composition points to inclusion of these polymers in the class of pectic polysaccharides. [Pg.558]

For monitoring the extent of polysaccharide hydrolysis, l.c. methods that sepeu ate and analyze the non-fermentable oligosaccharides (d.p. 3-30) derived from cellulose, hemicellulose, and pectins are useful, and have already been described (see Section III,l,c). For determination of the monosaccharide composition of completely hydrolyzed, plant polysaccharides, l.c. is especially useful and has been applied to the compositional analysis of hydrolyzed plant fiber,wood pulps,plant cell-walls,and cotton fibers.In these representative examples, the major sugars of interest, namely, glucose, xylose, galactose, arabinose, and mannose, have traditionally been difficult to resolve by l.c. The separa-... [Pg.52]

While the hemicelluloses obtained from the germ, aleuron, and caryopsis coat cell walls all showed a similar monosaccharide composition, this was not the case for the endosperm tissue. Thus, a major difference in the structure of hemicellulosic polysaccharides exists between the preparations obtained from the endosperm cell walls and those from the cell walls of the other parts of the grain, i.e., rice bran. (Rice bran consists of the caryopsis coat, aleuron layer and germ.) Comparison of the detailed structural features of the hemicellulosic polysaccharides of endosperm and bran cell walls will be discussed in the following sections. [Pg.336]

The present work deals with a two-step procedure of autohydrolysis followed by posthydrolysis to obtain a fermentable, monosaccharide-rich liquor from the hemicellulose fraction of BSG. The autohydrolysis step was carried out under preoptimized conditions, andboth enzymatic and chemical posthydrolysis were evaluated. Preliminary studies are also reported on the production of polyols from such liquor by Debaryomyces hansenii, a polyol-overproducing yeast (20-25). [Pg.1043]

Unlike starch or cellulose, BSG hemicellulose has a complex structure, which is still present, in part, on its autohydrolysis products. Oligosaccharides from BSG hydrolysis consist mainly of branched arabino-xylo-glucurono oligosaccharides that are not highly acetylated when compared to other xylans, such as from Eucalyptus wood (31). The action of several enzymatic activities including endo-l,4-P-xylanase P-xylosidase and accessory activities such as acetyl xylanesterase, a-glucuronidase, and a-arabino-furanosidase is therefore required for the complete hydrolysis of OCL to monosaccharides. [Pg.1047]

Hemicelluloses can be hydrolysed into their component sugars and used as a fermentation feedstock for the production of ethanol and other alcohols (e.g. butanol, arabitol, glycol and xylitol), organic acids (e.g. acetic acid), acetone and gases (e.g. methane and hydrogen). The wider monosaccharide profile offers opportunities to develop different products to those derived from glucose alone. [Pg.35]

Occurrence. D-Xylose (10) is present in widely abundant polysaccharides of plant tissues. Xylan is the main carbohydrate found in the hemicellulosic fraction, and accounts for one third of all renewable organic carbon available on earth. The structure and composition of xylans are variable, from linear (3-(l->4)-linked xylose chains to highly branched heteropolysaccharides. The branches may involve short oligosaccharides, usually of L-arabinofuranosyl units. Xyloglucans are also important hemicellulose polysaccharides consisting of a backbone of ( I — 4)-(i-D-glucopyranosyl residues heavily substituted with a-D-Xylp. Other monosaccharides may also be present.44... [Pg.16]

Chemically, about 35-55% of the dry material is the glucose polymer cellulose, much of which is in a crystalline structure while another 25—35% is hemicellulose, an amorphous polymer. The remainder is mostly lignin plus less amounts of minerals, waxes, and other compounds [3]. Cellulose is formed by beta-[l, 4] glucosyl linkages in a linear backbone, whereas hemicelluloses are branched polymers composed of several monosaccharides [5]. Fig. 1 shows the schematic illustration of the cellulose chain, while Fig. 2 shows the schematic illustration of xylans from Gramineae [5, 6]. [Pg.451]

However, to characterize the solubilized hemicelluloses of the wheat-straw samples, the four extracted fiactions obtained and the commercial hemieellulose of birch wood (Sigma ) were hydrolyzed to determine their sugar constituents, and the results are given in Table 2. The major monosaccharide obtained was xylose of birch wood (48.1%), indicating the presence of a xylan. In the hemicelluloses of wheat straw, the major monosaccharide was arabinose (36.5%), indicating the presence of an arabinoxylan. However, these sugar concentrations were very low which can likely be due to the methodology used to determined the chemical composition of the hemieellulose extracted from wheat straw. [Pg.456]


See other pages where Monosaccharides from hemicellulose is mentioned: [Pg.94]    [Pg.5]    [Pg.93]    [Pg.148]    [Pg.112]    [Pg.297]    [Pg.112]    [Pg.166]    [Pg.293]    [Pg.21]    [Pg.45]    [Pg.128]    [Pg.49]    [Pg.42]    [Pg.11]    [Pg.107]    [Pg.280]    [Pg.526]    [Pg.1041]    [Pg.1174]    [Pg.5]    [Pg.8]    [Pg.10]    [Pg.23]    [Pg.193]    [Pg.20]    [Pg.264]    [Pg.376]    [Pg.241]    [Pg.990]    [Pg.61]    [Pg.473]    [Pg.1530]    [Pg.291]    [Pg.259]    [Pg.278]    [Pg.21]    [Pg.174]    [Pg.232]   
See also in sourсe #XX -- [ Pg.102 ]




SEARCH



Hemicellulose

Hemicelluloses

© 2024 chempedia.info