Enhancement of trace organic contaminant degradation by crude enzyme extract from Trametes versicolor culture: Effect of mediator type and concentration

The performance of two redox mediating compounds, namely 1-hydroxybenzotriazole (HBT) and syringaldehyde (SA), was compared in terms of enhancement of enzymatic degradation of a diverse set of 14 phenolic and 16 non-phenolic trace organic contaminants (TrOCs) and the toxicity of the treated media. Extracellular enzyme extract (predominantly containing laccase) from Trametes versicolor culture achieved efficient degradation (70-95%) of nine phenolic and one non-phenolic TrOCs. Mediator dosing extended the spectrum of efficiently degraded TrOCs to 13 phenolic and three non-phenolic compounds, with moderate improvements in removal of a few other non-phenolic compounds. TrOC removal efficiency improved significantly as the HBT dose was increased from 0.1 to 0.5 mM, while SA achieved similar removal over dosage range of 0.1-1 mM. A particular concern was the toxicity of the treated media (1200-2200 times that of the control) for all SA dosages applied. Overall, HBT at a concentration of 0.5 mM achieved the best removal without raising concern regarding toxicity of the treated media. The results are discussed in the light of the redox potential of the enzyme-mediator cocktail, the balance between the stability and reactivity of the radicals generated and their cytotoxic effects

Impact of 1-hydroxybenzotriazole dosing on trace organic contaminant degradation by laccase

This study investigated the removal of five selected non-phenolic trace organic contaminants (TrOC) by extracellular enzyme extract from a white-rot fungus. Except diclofenac, no other investigated non-phenolic TrOC were degraded by the extracellular enzyme extract. Improvement of enzymatic degradation of all TrOC was achieved in the presence of a redox mediator, namely, 1-hydroxybenzotriazole (HBT). However, the enhancement of degradation was mediator concentration-specific. A significant improvement in degradation at higher dosage than 0.1 mM (HBT) was achieved