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Phytase production by Aspergillus niger and Aspergillus terreus in solid state fermentation using wheat bran
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phytase, solid state fermentation, Aspergillus
Animal nutrition industry demands for phytases with high specific activity and stability under high temperature conditions (feed pellet production) and under acidic conditions (monogastric animals), for this reason continues to stimulate the search for new enzyme sources [1]. Most of scientific work has been focused on Aspergillus spp. phytases due to their biochemical properties found [2]. An alternative for phytase production is solid state fermentation (SSF), it offers several advantages over submerged fermentation (SmF), as hiperglycosylated proteins, making them more stable, higher yields and productivities and can be used agroindustrial residues as substrate-support [3]. Wheat bran (agroindustrial residue) is one of the most used in phytase production by SSF, due to their high phytic acid concentration (1-2%) compared to other residues. It is important to give an adequate pretreatment to the residue in order to be used for phytase production avoiding contamination and preventing phytic acid hydrolysis [4]. Filamentous fungi (164) belonging to CIATEJ collection, isolated from different agroindustrial wastes and unconventional environments (mescal, cocoa fermentation, coffee pulp, etc.), were grown in a media using phytic acid as sole source of carbon and phosphorus in order to find phytase-producing candidates. A screening method using 15 mL tubes fermentation system was performed to assay different fermentation conditions at the same time, obtaining rapid and reliable results. The best fermentation conditions found using 15 mL tubes as reactor were: wheat bran without wash and UV exposed for 2h and culture media A; reaching a maximum phytase activity of 1.91±0.25 U/gdm at 192h of fermentation (Fig. 1-A). The other wheat bran pretreatments as well as culture media B do not present significant phytase activity (Fig. 1-B). Maximum phytase activity reached using columns reactors were: 4.2±0.71 U/gdm at 96h of culture for Aspergillus niger and 0.49±0.005 U/gdm at 96h for Aspergillus terreus (Fig. 2).
Asociación Mexicana de Ciencias de los Alimentos
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