BackgroundThe lignocellulosic enzymes of Trichoderma species have received particular attention with regard to biomass conversion to biofuels, but the production cost of these enzymes remains a significant hurdle for their commercial application. In this study, we quantitatively compared the lignocellulolytic enzyme profile of a newly isolated Trichoderma asperellum S4F8 strain with that of Trichoderma reesei Rut C30, cultured on sugarcane bagasse (SCB) using solid-state fermentation (SSF).ResultsComparison of the lignocellulolytic enzyme profiles of S4F8 and Rut C30 showed that S4F8 had significantly higher hemicellulase and β-glucosidase enzyme activities. Liquid chromatography tandem mass spectrometry analysis of the two fungal secretomes enabled the detection of 815 proteins in total, with 418 and 397 proteins being specific for S4F8 and Rut C30, respectively, and 174 proteins being common to both strains. In-depth analysis of the associated biological functions and the representation of glycoside hydrolase family members within the two secretomes indicated that the S4F8 secretome contained a higher diversity of main and side chain hemicellulases and β-glucosidases, and an increased abundance of some of these proteins compared with the Rut C30 secretome.ConclusionsIn SCB SSF, T. asperellum S4F8 produced a more complex lignocellulolytic cocktail, with enhanced hemicellulose and cellobiose hydrolysis potential, compared with T. reesei Rut C30. This bodes well for the development of a more cost-effective and efficient lignocellulolytic enzyme cocktail from T. asperellum for lignocellulosic feedstock hydrolysis.
Green tea extracts from the indigenous South African rooibos (Aspalathus linearis) and honeybush (Cyclopia species) plants were evaluated as potential antifungal agents against the plant pathogen Botrytis cinerea. When applied at 10 mg/ml, the tea extracts stimulated biomass production in B. cinerea by more than 3-fold after 24 hrs. This induction could not be linked directly to the presence of selected micro-and macronutrients or antioxidants in the extracts, suggesting a complex set of yet unidentified factors that may act synergistically to enhance cell growth. However, when applied at 100 mg/ml, the A. linearis and C. genistoides extracts reduced spore germination of B. cinerea by 33.3% and 16.7%, respectively. This suggests that the tea extracts contain active compounds that should be further investigated for their potential as natural anti-fungal agents.
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