Rueda, Andres; Doucet, Nicolas; Sanchez, Clara; Ospina, Sonia et Molina, Daniel . Characterization of laccase from native Dictyopanus pusillus In: 16e Symposium annuel de PROTEO, Mai 2016, Université Laval, Québec.
Ce document n'est pas hébergé sur EspaceINRS.Résumé
Lignolytic enzymes are a group of biocatalysts with potential applications in delignification and bioremediation. The enzymatic delignification process is a green chemistry alternative for the pretreatment of lignocellulosic material, providing a means for the efficient removal of lignin and the synthesis of biologically active compounds such as monolignols. Laccases (EC 1.10.3.2) are the most studied enzymes in delignification processes and Basidiomycete fungi are the main source. The aim of this study was to identify the gene sequence and protein structure of a protein band identified with a laccase activity from an enzymatic extract obtained by solid-state fermentation (SSF) of Dictyopanus pusillus. The enzymatic extract from D. pusillus was concentrated and purified by fast protein liquid chromatography (FPLC) using an anion exchanger. SDS-PAGE and native PAGE were used to determine the molecular weight and activity of the bands obtained. Tryptic digestion and Micro-HPLC-MS analyses were performed to identify peptides belonging to the protein band identified with laccase activity. From those peptides, degenerate primers were designed to amplify the coding gene sequence from D. pusillus. Three DNA sequences with high identity were obtained and have been used to elucidate the putative laccase gene. These results confirm the expression of a new laccase in D. pusillus, further allowing overproduction of this enzyme in a heterologous system.
| Type de document: | Document issu d'une conférence ou d'un atelier |
|---|---|
| Mots-clés libres: | - |
| Centre: | Centre INRS-Institut Armand Frappier |
| Date de dépôt: | 16 août 2018 02:43 |
| Dernière modification: | 13 juin 2023 20:11 |
| URI: | https://espace.inrs.ca/id/eprint/5805 |
Gestion Actions (Identification requise)
 |
Modifier la notice |