Biotransformation of the insecticide lindane by the white rot basidiomycete Phanerochaete chrysosporium has been investigated in liquid cultures. Some polar metabolites and carbon dioxide were produced from the pesticide. Among the metabolites identified were tetrachlorocyclohexene, tetrachlorocyclohexene epoxide and tetrachlorocyclohexenol. When used as a substrate, tetrachlorocyclohexene was also converted by the fungus to tetrachlorocyclohexenol, polar metabolites and carbon dioxide. Three incubation conditions leading to low and high peroxidase production were assayed. Data from these experiments, as well as in-vitro incubations with purified enzymes, ruled out any involvement of the peroxidases in lindane biotransformation and mineralization. Moreover, 1-aminobenzotriazole (a P450 inactivator) drastically reduced pesticide metabolism. Conversely, phenobarbital (a P450 inducer) did not significantly increase lindane breakdown.

Biotransformation of atrazine by the white rot fungus Phanerochaete chrysosporium was demonstrated by a 48% decrease of the initial herbicide concentration in the growth medium within the first 4 days of incubation, which corresponded to the mycelium-growing phase. Results clearly established the mineralization of the ethyl group of the herbicide. Analysis of the growth medium showed the formation of hydroxylated and/or N-dealkylated metabolites of atrazine during fungal degradation.

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: The ability of the white rot basidiomycete Phanerochaete chrysosporium to transform s-triazine herbicides has been investigated in laboratory experiments. The chlorinated metabolites formed during atrazine Ndealkylations were not further transformed by the fungus, whereas hydroxyatrazine was converted to an unknown product. P. chrysosporium was also able to carry out the N-dealkylation of the herbicides simazine, propazine and terbuthylazine. Herbicide metabolism was not supported by puriÐed peroxidases. The highest rates of herbicide N-dealkylation were obtained in liquid cultures maintained under moderate temperature allowing a long mycelium growing phase. Atrazine transformation was found to be supported by the mycelium, which contained signiÐcant amounts of microsomal cytochrome P450. Herbicide N-dealkylation was decreased in the presence of 1-aminobenzotriazole, in agreement with the involvement of P450 monooxygenases in atrazine metabolism.

The effect of nonylphenol on fungi following the application of contaminated sewage sludge on agricultural soil was studied in laboratory experiments. Nonylphenol bioavailability and adsorption were determined in the soil alone and soil-sludge mixtures. Mixing the soil with sludge made it possible to measure the nonylphenol concentration in the soil solution, which comprised between 6.6 x 10(-6) and 3.8 x 10(-7) M, according to the sludge. We then examined the dose-response relationship between nonylphenol concentration in the culture medium and both biomass production and germination rate of the spores from several strains of filamentous fungi. When applied in this range of concentration, nonylphenol was without noticeable short-term effect on these endpoints. Long-term exposure of fungi to nonylphenol was also assessed. The most intensive effect was a strong stimulation of spore production and germination in Fusarium oxysporum Schlechtendahl. Biomass production by the Fusarium strains also increased. Finally, nonylphenol was shown to induce laccase production in Trametes versicolor. We conclude that the potential of nonylphenol to adversely affect several soil fungi remains low.