7-15: Effect of initial moisture content on two Amazon rainforest Aspergillus strains cultivated on agroindustrial residues: biomass-degrading enzymes production and characterization

Monday, April 30, 2012
Napoleon Ballroom C-D, 3rd fl (Sheraton New Orleans)
Priscila da Silva Delabona1, Rosangela D. P. Buzon Pirota1, Carla Aloia Codima1, Célia Regina Tremacoldi2, Andre Rodrigues3 and Cristiane Sanchez Farinas1, (1)Brazilian Agricultural Research Corporation - Embrapa, São Carlos, Brazil, (2)Brazilian Agricultural Research Corporation - Embrapa, Belém, Brazil, (3)Universidade Estadual de Santa Cruz, Brazil
Biomass-degrading enzymes production using low cost and easily available agricultural residues as substrates of solid state fermentation (SSF) can contribute to a broader application of enzymes in the conversion process of biomass into biofuels. Among the operational parameters that affect the SSF process efficiency, moisture content is one of the most important. This work evaluates the initial moisture content effect on two Aspergillus strains isolated from the Amazon Rainforest growing under SSF by analyzing the biomass-degrading enzymes produced using different agro-industrial residues as carbon sources (wheat bran, sugar cane bagasse, soybean bran, and orange peel) and characterizing the enzymatic complex produced by a selected strain of Aspergillus fumigatus in terms of the optimum pH and temperature and thermal stability. Among the lignocellulosic materials evaluated as carbon source for Aspergillus cultivation, wheat and soybean bran as well as the mixture of sugar cane bagasse and wheat bran (1:1) were the most effective for multienzyme production. Nevertheless, much higher values for β-glucosidase and xylanase were achieved when using wheat bran as substrate. The characterization of the crude enzyme has shown A. fumigatus P40M2 enzymes to be active in the acidic pH range 3 to 5, with maximal activity at either pH 3.0 or 65 °C, hence a promising organism for the production of acidophilic and thermophilic enzymes.
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