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Different fungal laccases were used as biocatalysts for the biotransformation of bisphenol A (BPA). The quantitative analysis by gas chromatography-mass spectrometry (GCeMS) showed that BPA is more rapidly oxidized by Coriolopsis gallica laccase among the different fungal laccases tested. Carboxylic acid derivatives such as tartaric acid was found as BPA degradation products resulting from reactions catalyzed by 1 U ml 1 of laccase from C. gallica in the presence of 1 mM of the laccase-mediator 1-hydroxybenzotriazole (HBT), while b-hydroxybutyric acid resulted from oxidative reactions without HBT. BPA was completely removed within 3 h and pyroglutamic acid was found as a supplementary oxidative degradation product from HBT when identified by GCeMS. Laccase played a critical role in BPA biodegradation and catalyzed a cross-coupling reaction

This study concerns the decolorization and detoxification of the azo dye Acid Orange 51 (AO51) by crude laccase from Trametes trogii produced in solid culture using sawdust as support media. A three-level Box–Behnken factorial design with four factors (enzyme concentration, 1-hydroxybenzotriazole (HBT) concentration, dye concentration and reaction time) combined with response surface methodology was applied to optimize AO51 decolorization. A mathematical model was developed showing the effect of each factor and their interactions on color removal. The model predicted that Acid Orange 51 decolorization above 87.87 ± 1.27 % could be obtained when enzyme concentration, HBT concentration, dye concentration and reaction time were set at 1 U/mL, 0.75 mM, 60 mg/L and 2 days, respectively. The experimental values were in good agreement with the predicted ones and the models were highly significant, the correlation coefficient (R 2) being 0.9. Then the desirability function was employed to determine the optimal decolorization condition for each dye and minimize the process cost simultaneously. In addition, germination index assay showed that laccase-treated dye was detoxified; however in the presence of HBT, the phytotoxicity of the treated dye was increased. By using cheap agro-industrial wastes, such as sawdust, a potential laccase was obtained. The low cost of laccase production may further broaden its application in textile wastewater treatment.

This work represents the first report on the ability of autochthonous fungi of Tunisia to produce ligninolytic enzymes. Three hundred fifteen fungal strains were isolated from different Tunisian biotopes. These fungal strains were first screened for lignin-modifying enzymes on solid media containing Poly R-478 or ABTS. Of the 315 tested strains, 49 exhibited significant ABTS-oxidation activity, expressed within the first week of incubation and only 18 strains decolourised the Poly R-478. These positive strains were further screened in liquid culture and laccase, and lignin and Mn2+-oxidizing peroxidases activities were assayed. Of the 67 strains grown on liquid medium, 28 produced at least one of these 3 enzymes. The 8 highest producers of ligninolytic activities were identified by molecular techniques and 3 among them produced Lac, MnP and LiP simultaneously. New isolates reported in this work as fungi with significant ligninolytic activities includes Oxyporus, Stereum and Trichoderma. The isolated Trametes trogii CTM 10156 was the best Lac producer. Culture conditions and medium composition were optimised for this strain and resulted in high Lac production of 110 U ml-1 within 15 days of incubation (367 times higher than control medium).