Production, immobilization and thermodynamic studies of free and immobilized Aspergillus awamori amylase.

Int J Biol Macromol

Department of Chemistry of Natural and Microbial Products, National Research Centre, Dokki, Cairo, Egypt. Electronic address:

Published: September 2017

Enzyme cost, stability and its thermodynamic characteristics are the main criteria for industrial use. In this study, Aspergillus awamori amylase was constitutively produced using various agro-industrial wastes. Olive oil cake gave the highest activity (230U/g). The amylase was partially purified to 2.81-fold purification. Immobilization was achieved using different carriers by covalent binding. The novel carrier Ca alginate (Alg) starch (St)/polyethyleneimine (PEI)/glutaraldehyde (GA), showed the highest operational stability and was selected for further studies. The optimum temperature for the free and immobilized form was 50°C and 55-60°C, respectively. The immobilization process had a major role in improving enzyme thermal stability. In comparison to free enzyme, the immobilized form showed the highest optimum temperature, activation energy (E) and deactivation rate constants (k). Also, t, D-values (decimal reduction time), change in enthalpy (ΔH° kJmol), and Gibbs free energy (ΔG°) increased and was higher than the native enzyme within 50-80°C. The magnitude of negative value of entropy (ΔS° kJmol) for immobilized enzyme was negative for the free and immobilized enzymes revealing that native form of enzyme was in more ordered state. K and V values were slightly affected by the temperature variations 40-70°C.

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http://dx.doi.org/10.1016/j.ijbiomac.2017.04.033DOI Listing

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