Title of article :
Laccase-catalyzed decolorization and detoxification of Acid Blue 92: statistical optimization, microtoxicity, kinetics, and energetics
Author/Authors :
Rezaei، Shahla نويسنده 1Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, Tehran 14176, Iran , , Tahmasbi، Hamed نويسنده 1Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, P.O. Box 14155–6451, Tehran 1417614411, Iran , , Mogharabi، Mehdi نويسنده 1Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, P.O. Box 14155–6451, Tehran 1417614411, Iran 2Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 1417614411, Iran , , Ameri، Alieh نويسنده , , Forootanfar، Hamid نويسنده 1Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, Tehran , Iran,Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, Kerman, , , KHOSHAYAND، Mohammad Reza نويسنده , , Faramarzi، Mohammad Ali نويسنده ,
Abstract :
Background: In recent years, enzymatic-assisted removal of hazardous dyes has been considered as an alternative
and eco-friendly method compared to those of physicochemical techniques. The present study was designed in
order to obtain the optimal condition for laccase-mediated (purified from the ascomycete Paraconiothyrium variabile)
decolorization of Acid Blue 92; a monoazo dye, using response surface methodology (RSM). So, a D-optimal design
with three variables, including pH, enzyme activity, and dye concentration, was applied to optimize the decolorization
process. In addition, the kinetic and energetic parameters of the above mentioned enzymatic removal of Acid Blue 92
was investigated.
Results: Decolorization of Acid Blue 92 was maximally (94.1% ± 2.61) occurred at pH 8.0, laccase activity of 2.5 U/mL,
and dye concentration of 75 mg/mL. The obtained results of kinetic and energetic studies introduced the
laccase-catalyzed decolorization of Acid Blue 92 as an endothermic reaction (Ea, 39 kJ/mol; ?S, 131 J/mol K; and ?H,
40 kJ/mol) with Km and Vmax values of 0.48 mM and 227 mM/min mg, respectively. Furthermore, the results of microtoxicity
study revealed that the toxicity of laccase-treated dye was significantly reduced compared to the untreated dye.
Conclusions: To sum up, the present investigation introduced the Paraconiothyrium variabile laccase as an efficient
biocatalyst for decolorization of synthetic dye Acid Blue 92.