ABSTRACT
Decolourization activity of Phanerochaete chrysosporium for three synthetic dyes viz., congo red, malachite green and crystal violet and impact of additional carbon and nitrogen supply on decolourization capacity of fungus were investigated. Maximum decolourizing capacity was observed up to 15 ppm. Addition of urea as nitrogen source and glucose as carbon source significantly enhanced decolourizing capacity (up to 87%) of fungus. In all the cases, both colour and COD were reduced more in non-sterilized treatments as compared to sterilized ones. Significant reductions in COD content of dye solutions (79-84%) were recorded by fungus supplied with additional carbon and nitrogen. A highly significant correlation (r = 0.78, p < 0.001) between colour and COD of dye solutions was recorded. Thus, a readily available carbon and nitrogen source is imperative to enhance the bioremediation activity of this fungus which has been the most suitable for synthetic dyes and textile industry wastewater treatment.
Subject(s)
Biodegradation, Environmental , Carbon/chemistry , Color , Coloring Agents/chemistry , Congo Red/chemistry , Gentian Violet/chemistry , Nitrogen/chemistry , Oxygen/chemistry , Phanerochaete/drug effects , Rosaniline Dyes/chemistry , Textile Industry , Water Pollutants, ChemicalABSTRACT
In this report we describe the isolation and characterization of a gene encoding the transcription factor Acel (Activation protein of cup 1 Expression) in the white rot fungus Phanerochaete chrysosporium. Pc-acel encodes a predicted protein of 633 amino acids containing the copper-fist DNA binding domain typically found in fungal transcription factors such as Acel, Macl and Haal from Saccharomyces cerevisiae. The Pc-acel gene is localized in Scaffold 5, between coordinates 220841 and 222983. A S. cerevisiae acel null mutant strain unable to grow in high-copper medium was fully complemented by transformation with the cDNA of Pc-acel. Moreover, Northern blot hybridization studies indicated that Pc-acel cDNA restores copper inducibility of the yeast cup 1 gene, which encodes the metal-binding protein metallothionein implicated in copper resistance. To our knowledge, this is first report describing an Acel transcription factor in basidiomycetes.