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Cellulose fungal

Bonfante et al. (73) used monoclonal antibodies and enzyme-gold complexes to reveal pectins and cellulose at the interface between the fungal wall and the host plasma membrane in AM roots (Fig. 6), and additional wall components have been investigated with other molecular probes (74-76). These studies indicate that the interface is an apoplastic space of high molecular complexity where the boundaries of the partners are defined. The examination of other endomycorrhizal systems has demonstrated that their interface is morphologically similar but different in composition. Cellulose and pectins are present at the interface... [Pg.271]

In the treatment of cellulose pulps one essential criterion for a suitable enzyme preparation is that its cellulase activity should be as low as possible, or preferably absent completely. As even extremely low cellulase activities may ruin pulp quality, Trichoderma enzyme preparations are unlikely to be suitable for these applications. Many bacterial and fungal enzymes with low cellulase activity have been shown to be suitable for treatment of pulps 14, 15, 16,17), Regulation of the often synchronous production of cellulolytic and hemicellulolytic enzymes in micro-organisms is not well understood, and is further complicated by substrate cross-specificity of these enzymes. Enzymes with both endoglucanase and xylanase activity have been reported for bacteria 18, 19) and fungi 20, 21, 22), In addition to selection of strain and... [Pg.13]

Cost sensitivity studies have shown that the successful commercialization of cellulase-based processes, such as the conversion of cellulose to fermentable sugars, is highly dependent on the cost of enzyme production (i). Because fungal -D-glucosidase (EC 3.2.1.21) is the most labile enzyme in this system under process conditions (2), and k to efficient saccharification of cellulose, this enzyme was targeted for application of stabilization technology, both through chemical modification and immobilization to solid supports. [Pg.137]

In searching for means to enhance this in vitro activity, a range of fungal isolates were screened for cellulolytic activity on straw. The tests used to assay activity included clearing of cellulose agar (zone size measured), loss of weight from straw, colony radial extension rate on a water-soluble extract... [Pg.611]

DehnuUe, B., De Saeger, S., Adams, A., De Kimpe, N., and Van Peteghem, C., Development of a hquid chromatography/tandem mass spectrometry method for the simultaneous determination of 16 myco-toxins on cellulose filters and in fungal cultures, Rapid Communications in Mass Spectrometry 20(5), 771-776, 2006. [Pg.97]

Streptomycin, chemistry of, 3, 337-384 Structural chemistry, of fungal polysaccharides, 23, 367-417 of the hemicelluloses, 14, 429-468 Structure, molecular, of cellulose, 19, 219-246 of dextran, 15, 341-369 of glycogens, 12, 261-298 of polysaccharide gels and networks,... [Pg.537]

Chitin is the microfibrillar component of some fungal cell walls and is equivalent to cellulose microfibrils in plants. It is a characteristic feature of the Ascomycetes, Deuteromycetes and Basidiomycetes but is absent in the Phycomycetes, which contain cellulose as their major cell wall constituent. [Pg.94]

Polyoxins are inhibitors of chitin biosynthesis. Chitin is a component of fungal cell walls except in Phycomycete fungi these contain cellulose as their major cell wall constituent, hence polyoxins are inactive against Plasmopara, Pythium and Phytophthora. [Pg.135]

Cellulose, the most abundant of all biopolymers, is extremely stable but is attacked by a host of bacterial and fungal (3-glycanases.96 Animals do not ordinarily produce cellulases but some termites do.97 Cellulase structures are varied, being represented by 10 of 57 different glycosylhydrolase families.98 Most, like lysozyme, retain the P configuration in their products but some invert.98 100... [Pg.602]

Chitin. Like cellulose synthase, fungal chitin synthases are present in the plasma membrane and extrude microfibrils of chitin to the outside.147 150 In the fungus Mucor the majority of the chitin synthesized later has its N-acetyl groups removed hydrolytically to form the deacetylated polymer chitosan.151152 Chitin is also a major component of insect exoskeletons. For this reason, chitin synthase is an appropriate target enzyme for design of synthetic insecticides.153... [Pg.1148]

All naturally occurring fungal strains of Trichoderma require an inducer for cellulase synthesis. In the absence of an inducer such as cellulose, cellobiose (21,22), or sophorose (12,13,14,23), Trichoderma does not make any detectable cellulase complex enzymes. The true physiological inducer of cellulase is currently unknown. Insoluble cellulose is presumably not such an inducer since there is no way for the internal cell machinery to sense the presence of this insoluble material. However, a small transglycosylation product such as sophorose, 2-0-/ -glucopyranosyl-D-glucose, may well be the natural inducer. [Pg.290]


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