The decolorization/degradation of aqueous azo dyes generated by textile photography industries are a main issue in wastewater treatment. Despite many significant efforts and numerous systems have been exploited, the problem is still unsolved due to intrinsically low activity or use of non-convenient chemical reagents. Biodegradation appears to be
one of the most efficient ways, however, the initial step of biotransformation usually involves a reductive cleavage of the azo bond, which under anaerobic conditions leads to the formation of aromatic amines known to be carcinogenic. This study shows that applying an oxidative process of H
2O
2 catalyzed by chloroperoxidase (CPO) for decolorization/degradation of aqueous azo dyes (Orange G and Sunset Yellow) in buffer solution is a very efficient system. The effect of initial pH,
dosage of enzyme, H
2O
2 concentration, reaction temperature and
time, and suitable initial dye concentration on the decolorization efficiency were investigated in detail and optimized accordingly. At optimum reaction condition, the decolorization efficiency of Orange G reached 98.72%in 5 min, and 77.25%in 10 min for Sunset Yellow. The
dosage of CPO was below ppm level. This enzymatic reaction is an ideal potential alternative for application on decolorization/degradation of aqueous azo dyes.
Furthermore, the elucidation of degradation pathways is of special interest considering healthy and environmental priorities. In this work, LC-MS was used to determine the structures of intermediates arising from Orange G by CPO-H2O2 oxidation. Eight transformation products were identified and two types of cleavage were proposed for the degradation pathway.