Application of Deconica castanella ligninolytic enzymatic system in the degradation of hexachlorobenzene in soil.
Sergio Luiz Moreira NetoGlauciane Danusa CoelhoNara BallaminutDácio Roberto MatheusDouglas Vieira ThomazKatia Maria Gomes MachadoPublished in: Biotechnology and applied biochemistry (2021)
Hexachlorobenzene (HCB) is a pollutant still found in the environment despite being widely banned. Considering that basidiomycetes are useful to degrade a variety of organochlorinated pollutants, we therefore report the influence of HCB on the the ligninolytic enzymatic system of Deconica castanella. The Inoculum was prepared with sugarcane bagasse and soybean flour, and was added in soil with and without HCB (2000 mg Kg soil-1 ), 5% emulsion containing soybean oil and tween 20 at proportion 9:1, v:v; with 70% moisture at 25° C. Fungal biomass was quantified by widely acknowledged growth biomarker ergosterol. The extraction of the enzymatic complex was performed and laccase, Mn-dependent peroxidase (MnP) and lignin peroxidase (LiP) activities were determined. Furthermore, HCB and its metabolites were quantified by gas chromatography and chlorides by potentiometric titration. Results evidenced that HCB did not interfere in fungal growth, though the only detected enzymatic activity was laccase. MnP e Lip were not detected during D. castanella growth in soil. The peak of laccase enzymatic activity occurred in the presence of HCB. In addition, the laccase exhibited thermostability. Therefore, we hereby shed light on the role of laccase in the degradation of HCB by an efficient low-cost and environmentally safe detoxification mechanism. This article is protected by copyright. All rights reserved.