Fungal Laccases and Fumonisin Decontamination in Co-Products of Bioethanol from Maize
Marianela Bossa,
Noelia Edith Monesterolo,
María del Pilar Monge,
Paloma Rhein,
Sofía Noemí Chulze,
María Silvina Alaniz-Zanon,
María Laura Chiotta
Affiliations
Marianela Bossa
Instituto de Investigación en Micología y Micotoxicología (IMICO), CONICET-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
Noelia Edith Monesterolo
Instituto de Biotecnología Ambiental y de la Salud (INBIAS), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
María del Pilar Monge
Instituto de Investigación en Micología y Micotoxicología (IMICO), CONICET-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
Paloma Rhein
Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
Sofía Noemí Chulze
Instituto de Investigación en Micología y Micotoxicología (IMICO), CONICET-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
María Silvina Alaniz-Zanon
Instituto de Investigación en Micología y Micotoxicología (IMICO), CONICET-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
María Laura Chiotta
Instituto de Investigación en Micología y Micotoxicología (IMICO), CONICET-Universidad Nacional de Río Cuarto (UNRC), Ruta Nacional 36 Km 601, Río Cuarto 5800, Argentina
Maize (Zea mays L.) may be infected by Fusarium verticillioides and F. proliferatum, and consequently contaminated with fumonisins (FBs), as well as the co-products of bioethanol intended for animal feed. Laccase enzymes have a wide industrial application such as mycotoxin degradation. The aims were to isolate and identify fungal laccase-producing strains, to evaluate laccase production, to determine the enzymatic stability under fermentation conditions, and to analyse the effectiveness in vitro of enzymatic extracts (EEs) containing laccases in degrading FB1. Strains belonging to Funalia trogii, Phellinus tuberculosus, Pleurotus ostreatus, Pycnoporus sanguineus and Trametes gallica species showed laccase activity. Different isoforms of laccases were detected depending on the evaluated species. For the FB1 decontamination assays, four enzymatic activities (5, 10, 15 and 20 U/mL) were tested, in the absence and presence of vanillic acid (VA) and 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) as redox mediators (1 and 10 mM). Trametes gallica B4-IMICO-RC EE was the most effective strain in buffer, achieving a 60% of FB1 reduction. Laccases included in EEs remained stable at different alcoholic degrees in maize steep liquor (MSL), but no significant FB1 reduction was observed under the conditions evaluated using MSL. This study demonstrate that although laccases could be good candidates for the development of a strategy to reduce FB1, further studies are necessary to optimise this process in MSL.