Fabrication of a biocathode for formic acid production upon the immobilization of formate dehydrogenase from Candida boidinii on a nanoporous carbon

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dc.contributorElectroquímica Aplicada y Electrocatálisises_ES
dc.contributor.authorHernández Ibáñez, Naiara-
dc.contributor.authorGomis-Berenguer, Alicia-
dc.contributor.authorMontiel, Vicente-
dc.contributor.authorAnia, Conchi O.-
dc.contributor.authorIniesta, Jesus-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Físicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Electroquímicaes_ES
dc.date.accessioned2021-12-02T08:24:22Z-
dc.date.available2021-12-02T08:24:22Z-
dc.date.issued2021-11-30-
dc.identifier.citationChemosphere. 2022, 291(Part 3): 133117. https://doi.org/10.1016/j.chemosphere.2021.133117es_ES
dc.identifier.issn0045-6535 (Print)-
dc.identifier.issn1879-1298 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/119969-
dc.description.abstractThe immobilization of the non-metallic enzyme formate dehydrogenase from Candida boidinii (CbFDH) into a nanoporous carbon with appropriate pore structure was explored for the bioelectrochemical conversion of CO2 to formic acid (FA). Higher FA production rates were obtained upon immobilization of CbFDH compared to the performance of the enzyme in solution, despite the lower nominal CbFDH to NADH (β-nicotinamide adenine dinucleotide reduced) cofactor ratio and the lower amount of enzyme immobilized. The co-immobilization of the enzyme and a rhodium complex as mediator in the nanoporous carbon allowed the electrochemical regeneration of the cofactor. Preparative electrosynthesis of FA carried out on biocathodes of relatively large dimensions (ca. 3 cm × 2 cm) confirmed the higher production rate of FA for the immobilized enzyme. Furthermore, the incorporation of a Nafion binder in the biocathodes did not modify the immobilization extent of the CbFDH in the carbon support. Coulombic efficiencies close to 46% were obtained for the electrosynthesis carried out at −0.8 V for the biocathodes prepared using the lowest Nafion binder content and the co-immobilized enzyme and rhodium redox mediator. Although these values may yet be improved, they confirm the feasibility of these biocathodes in larger scales (6 cm2) beyond most common electrode dimensions reported in the literature (ca. a few mm2).es_ES
dc.description.sponsorshipNH, VM and JI thank Spanish MINICINN (projects CTQ2016-76231-C2-2-R and PID2019-108136RB-C32) for financial support. COA thanks the financial support of the European Research Council through a Consolidator Grant (PHOROSOL 684161).es_ES
dc.languageenges_ES
dc.publisherElsevieres_ES
dc.rights© 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).es_ES
dc.subjectFormate dehydrogenase from Candida boidiniies_ES
dc.subjectFormic acid NADH-Regenerationes_ES
dc.subjectMesoporous carbones_ES
dc.subjectBiocathodees_ES
dc.subject.otherQuímica Físicaes_ES
dc.titleFabrication of a biocathode for formic acid production upon the immobilization of formate dehydrogenase from Candida boidinii on a nanoporous carbones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1016/j.chemosphere.2021.133117-
dc.relation.publisherversionhttps://doi.org/10.1016/j.chemosphere.2021.133117es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2016-76231-C2-2-Res_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108136RB-C32es_ES
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