Production of extracellular enzyme by the white-rot fungus Dichomitus squalens in cellulose-containing liquid culture

The white-rot fungus Dichomitus squalens has been found to be a potent endo-1,4-β- d-glucanase producer when cultivated on crystalline cellulose in the presence of 0.2% proteose peptone. Several activities were detected in culture supernatant, including endo-1,4-β- d-glucanase [1,4-(1,3;1,4)-β- d-gl...

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Veröffentlicht in:Enzyme and microbial technology 1986, Vol.8 (1), p.22-26
Hauptverfasser: Rouau, X., Odier, E.
Format: Artikel
Sprache:eng
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Zusammenfassung:The white-rot fungus Dichomitus squalens has been found to be a potent endo-1,4-β- d-glucanase producer when cultivated on crystalline cellulose in the presence of 0.2% proteose peptone. Several activities were detected in culture supernatant, including endo-1,4-β- d-glucanase [1,4-(1,3;1,4)-β- d-glucan 4-glucanohydrolase, EC 3.2.1.4], d-xylanase (endo-1,3-β- d-xylanase, 1,3-β- d-xylan xylanohydrolase, EC 3.2.1.32), exopoly- d-galacturonase [poly(1,4-α- d-galacturonide) galacturonohydrolase, EC 3.2.1.67], cellobiose dehydrogenase [cellobiose:quinone oxidoreductase, see d-glucose dehydrogenase (acceptor), d-glucose:(acceptor) 1-oxidoreductase, EC 1.1.99.10], β- d-glucosidase (β- d-glucoside glucohydrolase, EC 3.2.1.21) and exo-cellobiohydrolase (1,4-β- d-glucan cellobiohydrolase, EC 3.2.1.91), using 4-nitrophenyl-β- d-cellobioside as a substrate. A crude enzyme preparation was obtained by ammonium sulphate (80% saturation) precipitation of soluble protein. In spite of the presence of both endo- and exo-β- d-glucanase activities, degradation of crystalline cellulose by the enzymic preparation remained weak.
ISSN:0141-0229
1879-0909
DOI:10.1016/0141-0229(86)90005-0