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The aliquot (3 ml) of the culture media was withdrawn at different time intervals, centrifuged at 6000 g for 20 min and the decolourization was determined by measuring the change in absorbance of culture supernatants at kmax of the respective dyes. Change in pH and reduction in COD (APHA 1995) was studied during Brown 3REL decolourization. Growth of micro-organism in dye containing medium was determined by the gravimetric method, after drying at 80_C until constant weight. The percentage of decolourization (Saratale et al. 2006) and average decolourization rate (ADR) (Khehra et al. 2005) were measured at different time intervals. All decolourization experiments were performed in triplicate. Abiotic controls (without micro-organisms) were always included. The ADR was calculated as follows: where, C = initial concentration of dye (mg l)l), %D = dye decolourization (%) after time t.

Average Decolourization Rate

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Page 1: Average Decolourization Rate

The aliquot (3 ml) of the culture media was withdrawnat different time intervals, centrifuged at 6000 g for20 min and the decolourization was determined by measuringthe change in absorbance of culture supernatantsat kmax of the respective dyes. Change in pH and reductionin COD (APHA 1995) was studied during Brown3REL decolourization. Growth of micro-organism in dyecontaining medium was determined by the gravimetricmethod, after drying at 80_C until constant weight. Thepercentage of decolourization (Saratale et al. 2006) andaverage decolourization rate (ADR) (Khehra et al. 2005)were measured at different time intervals. All decolourizationexperiments were performed in triplicate. Abioticcontrols (without micro-organisms) were alwaysincluded. The ADR was calculated as follows:

where, C = initial concentration of dye (mg l)l),%D = dye decolourization (%) after time t.