This study aimed to produce, characterize and purify a protease from Aspergillus heteromorphus URM0269. After production by solid fermentation of wheat bran performed according to a central composite design, protease was characterized in terms of biochemical, kinetic, and thermodynamic parameters for further purification by chromatography. Proteolytic activity achieved a maximum value of 57.
View Article and Find Full Text PDFCollagenolytic proteases produced by URM0269 were extracted using a PEG/sulfate aqueous two-phase system (ATPS). A 2 factorial design was performed to analyze the independent variables: PEG molar mass (M), PEG concentration (C), and sulfate concentration (C). The extracted proteases were also evaluated for their optimum pH and stability at different pH levels (4.
View Article and Find Full Text PDF