A. Persiani
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Papers by A. Persiani
relatively non-specific activities. In this research, we have investigated the potential of a saprotrophic soil fungus, Penicillium griseofulvum Dierckx, isolated from soils with high concentrations of isomers of hexachlorocyclohexane, to biotransform b-HCH, the most recalcitrant isomer to microbial activity. The growth kinetics of the fungus were characterized after growth in stirred liquid Czapek-Dox medium. It was found that P. griseofulvum was able to grow in the presence of 1 mg L1 b-HCH and in stressful nutritional conditions at different concentrations of sucrose in the medium (0 and 5 g L1). The effects of b-HCH and the toluene, used as a solvent for b-HCH addition, on P. griseofulvum were investigated by means of a Phenotype MicroArray™ technique, which suggested the activation of certain metabolic pathways as a response to oxidative stress due to the presence of the xenobiotics. Gas chromatographic analysis of b-HCH concentration confirmed biodegradation of the isomer with a minimum value of b-HCH
residual concentration of 18.6%. The formation of benzoic acid derivatives as dead-end products of b-HCH biotransformation was observed and this could arise from a possible biodegradation pathway for b-HCH with important connections to fungal secondary metabolism.
relatively non-specific activities. In this research, we have investigated the potential of a saprotrophic soil fungus, Penicillium griseofulvum Dierckx, isolated from soils with high concentrations of isomers of hexachlorocyclohexane, to biotransform b-HCH, the most recalcitrant isomer to microbial activity. The growth kinetics of the fungus were characterized after growth in stirred liquid Czapek-Dox medium. It was found that P. griseofulvum was able to grow in the presence of 1 mg L1 b-HCH and in stressful nutritional conditions at different concentrations of sucrose in the medium (0 and 5 g L1). The effects of b-HCH and the toluene, used as a solvent for b-HCH addition, on P. griseofulvum were investigated by means of a Phenotype MicroArray™ technique, which suggested the activation of certain metabolic pathways as a response to oxidative stress due to the presence of the xenobiotics. Gas chromatographic analysis of b-HCH concentration confirmed biodegradation of the isomer with a minimum value of b-HCH
residual concentration of 18.6%. The formation of benzoic acid derivatives as dead-end products of b-HCH biotransformation was observed and this could arise from a possible biodegradation pathway for b-HCH with important connections to fungal secondary metabolism.