Second generation ethanol is produced from the degradation of lignocellulosic biomass using enzymes as catalysts, with emphasis on xylanases. These biocatalysts are often costly, but stable at high temperatures, and t...Second generation ethanol is produced from the degradation of lignocellulosic biomass using enzymes as catalysts, with emphasis on xylanases. These biocatalysts are often costly, but stable at high temperatures, and their reuse is of great value, so the immobilization of the enzymes can increase their applicability on an industrial scale. We sought to immobilize a cocktail rich in xylanase produced by the fungus <i>Fusarium sp</i><i>.</i> EA 1.3.1 in alginate spheres, optimize the immobilization method, characterize the immobilized derivatives, improve their physical-chemical characteristics, and perform the hydrolysis of sugarcane bagasse to release sugars. The <i>Fusarium sp</i><i>.</i> EA 1.3.1 has been identified and used for cocktail rich in xylanase production that was immobilized in alginate spheres. During this process, the drip equipment, and the concentration of the solutions of sodium alginate and calcium chloride were evaluated. The best results were obtained with the glass rod and with concentrations of 3.14% and 2.10% for the solutions, respectively. The apparent optimum conditions of pH and temperature reaction were studied, and the values of pH 6.5 and 60°C were obtained. The immobilized conjugate also presented greater stability at this temperature than that of the soluble cocktail. The conjugate could be recycled up to six times, and its activity was maintained after 75 days of storage. Finally, the hydrolysis in natural sugarcane bagasse was achieved, and greater amounts of reducing sugars were obtained in the reaction with the conjugate. Thus, the cocktail rich in xylanase produced by the fungus <i>Fusarium sp.</i> EA1.3.1 was successfully immobilized on alginate spheres and possesses the potential to be used as a catalyst in industrial processes such as the lignocellulosic ethanol industry.展开更多
文摘Second generation ethanol is produced from the degradation of lignocellulosic biomass using enzymes as catalysts, with emphasis on xylanases. These biocatalysts are often costly, but stable at high temperatures, and their reuse is of great value, so the immobilization of the enzymes can increase their applicability on an industrial scale. We sought to immobilize a cocktail rich in xylanase produced by the fungus <i>Fusarium sp</i><i>.</i> EA 1.3.1 in alginate spheres, optimize the immobilization method, characterize the immobilized derivatives, improve their physical-chemical characteristics, and perform the hydrolysis of sugarcane bagasse to release sugars. The <i>Fusarium sp</i><i>.</i> EA 1.3.1 has been identified and used for cocktail rich in xylanase production that was immobilized in alginate spheres. During this process, the drip equipment, and the concentration of the solutions of sodium alginate and calcium chloride were evaluated. The best results were obtained with the glass rod and with concentrations of 3.14% and 2.10% for the solutions, respectively. The apparent optimum conditions of pH and temperature reaction were studied, and the values of pH 6.5 and 60°C were obtained. The immobilized conjugate also presented greater stability at this temperature than that of the soluble cocktail. The conjugate could be recycled up to six times, and its activity was maintained after 75 days of storage. Finally, the hydrolysis in natural sugarcane bagasse was achieved, and greater amounts of reducing sugars were obtained in the reaction with the conjugate. Thus, the cocktail rich in xylanase produced by the fungus <i>Fusarium sp.</i> EA1.3.1 was successfully immobilized on alginate spheres and possesses the potential to be used as a catalyst in industrial processes such as the lignocellulosic ethanol industry.
