| Literature DB >> 35142302 |
Ilaria Sorrentino1, Marie Carrière1, Hélène Jamet1, Ilaria Stanzione2, Alessandra Piscitelli2, Paola Giardina2, Alan Le Goff1.
Abstract
We investigated the use of POXA1b laccase from Pleurotus ostreatus for the oxidation of anthracene into anthraquinone. We show that different pathways can occur depending on the nature of the redox mediator combined to laccase, leading to different structural isomers. The laccase combined with 2,2'-azine-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) leads to the formation of 1,4-anthraquinone and/or 1,2-anthraquinone. The unprecedented role of carbon nanotubes (CNTs) as redox mediators for oxidation of anthracene into 9,10-anthraquinone is shown and corroborated by density-functional theory (DFT) calculations. Owing to the efficient adsorption of anthraquinones at CNT electrodes, anthracene can be detected with low limit-of-detection using either laccase in solution, CNT-supported laccase or laccase immobilized at magnetic beads exploiting the adhesive property of a chimeric hydrophobin-laccase.Entities:
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Year: 2022 PMID: 35142302 DOI: 10.1039/d1an02091a
Source DB: PubMed Journal: Analyst ISSN: 0003-2654 Impact factor: 4.616