Fractionation and identification of cellulases and other extracellular enzymes produced by Sporotrichum (Chrysosporium) thermophile during growth on cellulose or cellobiose
- 1 September 1983
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Microbiology
- Vol. 29 (9) , 1071-1080
- https://doi.org/10.1139/m83-165
Abstract
The extracellular enzyme proteins secreted by Sporotrichum (Chrysosporium) thermophile, ATCC 42 464, upon growth on cellulose or cellobiose, were separated by polyacrylamide gel electrophoresis and electrofocusing into different fractions which were then analyzed with respect to their enzymatic character to identify the cellulolytic enzymes. A positive reaction against carboxymethylcellulose azure (CMC azure) was taken as evidence for an endo-acting cellulase, whereas the criterion for the presence of an exo-cellulase was a negative reaction with CMC azure and a concomitant increase in reducing power upon action of any kind of cellulose. With this procedure, four main cellulolytic enzymes were detected: three endo-cellulases, named endo-cellulases I, II, and III (with corresponding isoelectric points 5.1, 4.2, 5.7), and an exo-cellulase (isoelectric point 4.7). With respect to their enzymatic action on amorphous cellulose, endo-cellulases I and III were isofunctional, releasing cellobiose and cellodextrins as hydrolytic products, whereas endo-cellulase II was found to produce additionally some glucose. Endo-cellulases I and III were also able to attack native (crystalline) cellulose like filter paper or Avicel, but endo-cellulase II could not and thus behaved as a true carboxymethylcellulase. The rate of formation of endo-cellulase I during growth was distinctly superior from that of the other cellulases so that the proportion of the activity due to endo-cellulase. I compared with that due to the others constantly increased during the culture.This publication has 12 references indexed in Scilit:
- Isolation of cellulases by means of biospecific sorption on amorphous celluloseAnalytical Biochemistry, 1981
- Separation and Some Properties of Two Intracellular β-Glucosidases of Sporotrichum (Chrysosporium) thermophileApplied and Environmental Microbiology, 1981
- Regulation of the cellulolytic system in Trichoderma reesei by sophorose: induction of cellulase and repression of beta-glucosidaseJournal of Bacteriology, 1980
- New chromogenic substrates for the assay of alpha-amylase and (1→4)-β-d-glucanaseCarbohydrate Research, 1980
- Analysis of cellulase proteins by high-performance liquid chromatographyJournal of Chromatography A, 1979
- Induction and Catabolite Repression of Cellulase Synthesis in the Thermophilic Fungus Sporotrichum thermophileJournal of General Microbiology, 1979
- Cell wall-degrading enzymes of vascular wilt fungi. II. Properties and modes of action of polysaccharidases of Verticillium albo-atrum and Fusarium oxysporum f. sp. lycopersiciPhysiological Plant Pathology, 1978
- Plant Microbody Proteins, I. Purification and Characterization of Catalase from Leaves ofLens culinarisHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1976
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951
- A COLORIMETRIC METHOD FOR THE DETERMINATION OF THE PROTEOLYTIC ACTIVITY OF DUODENAL JUICEJournal of Biological Chemistry, 1947