Peroxidase Essay

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Peroxidases enzymes are broadly distributed in microorganisms, and animals, where these play specific roles. However they are also present in plants abundantly and have been involved in several biochemical and physiological processes, such as in the protection mechanism in tissues infected and damage physically, participation in lignification process, and in the elimination of toxic effects of hydrogen peroxide which is produced during redox reaction. (Bhatti et al., 2012). Peroxidases contain haem proteins and have prosthetic group of iron (III) protoporphyrin IX (ferriprotoporphyrin IX). This is an assembly of oxidoreductases which catalyze the peroxiase reduction, like H2O2 and the oxidation of different inorganic and organic complexes (Hamid and Rehman., 2009). Dyes, the complicated aromatic substances mostly used to colorize different materials. Sometimes they combine on structural area with heavy metals, are examined to have comparatively unsatisfactory results on the nearby environment because of its inhibitory and toxic response (Mohan et al., 2005). About 10,000 diverse species of pigments and dyes are used in industries, which show that an annual use of almost 7×105 tonnes in world. Dyes are intractable and toxic materials, they oppose biological breakdown (Souza et al., 2007). Many industries like papers, textiles, gasoline, and leather are huge users of azo dyes which contains the largest group of substitute organic chemicals. The waste produced from these industries and resulting by-products have both metal ions and dyes. These waste products become hazardous when present in the surroundings. The insolvable dyes have low decomposability and only 45–47% dyes materials are known as biodegradable (Rauf and Ashraf., 2012)... ... middle of paper ... ... maximum decolorization of 97 and 77% was detected for Solar Blue A and Solar Flavine 5G at and temperature 50ºC and pH 4 respectively. They observed that by increasing incubation time and enzyme units, the % decolourization also enhanced. H2O2 dose of 0.7mM for Salar Flavin 5G and 0.8mM for Solar Blue A was enough for the dye degradation. Cordoba et al (2012). determined catalytic activity of hematin for dye degradation. 92% color removal was noticed for 75 mg l_1 solutions. They presented their results using Doehlert array. They noticed hematin as an effective azo dye removing agent. Boucherit et al. (2013) used Cucurbita pepo (courgette) peroxidase to decolorize Direct Yellow (DY106) and azo dyes. They also noticed the effect of temperature, pH, concentration of H2O2 and enzyme on degradation. The decolourization of DY106 was verified by UV-Vis analysis.

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