- MeSH
- Amplified Fragment Length Polymorphism Analysis methods MeSH
- DNA, Bacterial genetics chemistry MeSH
- DNA Fingerprinting methods MeSH
- Ecosystem MeSH
- Isotope Labeling MeSH
- Membrane Lipids analysis MeSH
- Environmental Microbiology MeSH
- Electrophoresis, Gel, Pulsed-Field methods MeSH
- Sequence Analysis, DNA methods MeSH
Liquid cultures with cellulose and solid state fermentation cultures on wheat straw of the white-rot fungi Pleurotus ostreatus and Trametes versicolor and the brown-rot fungus Piptoporus betulinus were assayed for the free and solid fraction-bound activity of lignocellulose-degrading enzymes. The majority of the ligninolytic enzymes laccase and Mn peroxidase was detected in the free fraction of P. ostreatus and T. versicolor. The endocleaving enzymes endo-1,4-beta-glucanase, endo-1,4-beta-mannanase and endo-1,4-beta-xylanase were detected almost exclusively in the free fraction, while significant amounts of 1,4-beta-glucosidase, cellobiohydrolase, 1,4-beta-xylosidase and 1,4-beta-mannosidase were present in the bound fraction depending on the mode of cultivation and the species. The bound enzymes accounted for 66% of the total activity in P. ostreatus straw cultures, 35% in T. versicolor and only 8% in P. betulinus. The enzymes also showed significant differences in freeze-drying stability. Hydrolases in general showed high stability, whereas laccase and Mn peroxidase of P. ostreatus were the least stable.
- MeSH
- Cellulases analysis MeSH
- Cellulose metabolism MeSH
- Enzymes analysis MeSH
- Financing, Organized MeSH
- Fungal Proteins analysis MeSH
- Glycoside Hydrolases analysis MeSH
- Culture Media chemistry MeSH
- Laccase analysis MeSH
- Lignin metabolism MeSH
- Freeze Drying MeSH
- Peroxidases analysis MeSH
- Pleurotus enzymology MeSH
- Polyporales enzymology MeSH
- Enzyme Stability MeSH
