par Vieira Monclaro, Antonielle
;Gonçalves, Thiago Augusto
;Magri, Silvia
;Ovaert, Justin
;Decembrino, Davide
;Debecker, Damien D.P.;Kadowaki, Marco Antonio
;Doneux, Thomas
;De Leener, Gaël
;Zarattini, Marco
;Luhmer, Michel
;Cannella, David 
Référence ChemCatChem, 15, 20, page (e202300602)
Publication Publié, 2023-09-01











Référence ChemCatChem, 15, 20, page (e202300602)
Publication Publié, 2023-09-01
Article révisé par les pairs
Résumé : | Abstract Melanin is a class of hetero-polymer pigments commonly found in nature and widely in fungi. Often referred to as the “animal lignin“, melanin is a very abundant bioresource and features many catalytically interesting properties. We conceived that, upon light absorbance, the polymer could promote long-distance electron donation to fuel redox enzymatic catalysis or controlled in-situ generation of H2O2. Here, we report on a fungal photo-biocatalytic system extracted from the commercially relevant A. nidulans, where photoactivated melanin acts as an electron donor for the cellulose-degrading AnAA9A and TtAA9E metalloenzymes. Furthermore, there was a stable and significant accumulation of H2O2 when melanin was irradiated by visible light; having the peroxide functioning as a co-substrate for the AA9 LPMO enzymes. Oxidized cellulose-derived oligosaccharides were detected in the dark and under light conditions, confirming the potential of melanin to reduce AA9s. When placed under light conditions, they provided hydrogen peroxide as a co-substrate for AA9s. The use of light to tune the in-situ generation of H2O2 by natural pigments might be pivotal to enable also another peroxide-dependent enzymatic catalysis. |