Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/26344
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dc.contributor.authorToledo, Mariah L.pt_PT
dc.contributor.authorPereira, Matheus M.pt_PT
dc.contributor.authorFreire, Mara G.pt_PT
dc.contributor.authorSilva, João P. A.pt_PT
dc.contributor.authorCoutinho, João A. P.pt_PT
dc.contributor.authorTavares, Ana P. M.pt_PT
dc.date.accessioned2019-07-31T17:57:16Z-
dc.date.issued2019-05-31-
dc.identifier.urihttp://hdl.handle.net/10773/26344-
dc.description.abstractThe research on alternative solvents and co-solvents is a relevant aspect when envisioning the improvement of biocatalytic reactions. Among these solvents and co-solvents, deep eutectic solvents (DES) may be considered as customizable new reaction media for biocatalysis. Accordingly, in this work, sixteen DES aqueous solutions, as well as of the individual DES components at the same conditions have been investigated in laccase-catalyzed reactions. Cholinium- and betaine-based DES formed with polyols at different molar ratio and concentrations were evaluated. The results reported show that in presence of most DES the laccase activity is preserved and, with a particular DES, enhanced up to 200%. Molecular docking studies demonstrated that while most DES components establish hydrogen-bonds with the enzyme amino acids, those that establish stronger interactions with the enzyme (expressed by absolute values of docking affinity energies) lead to an enhanced laccase activity. Finally, the laccase stability was evaluated in additional tests under extreme storage temperatures (60 ºC and -80 ºC). Although no significant protection to high temperatures was afforded by DES, an enhanced laccase activity when stored at low temperatures was found, at least up to 20 days. Combining experimental results and molecular docking this work shows that DES can be designed as co-solvents to improve biocatalytic reactions.pt_PT
dc.description.sponsorshipThis work was developed within the scope of the project CICECO-Aveiro Institute of Materials, FCT Ref. UID/CTM/50011/2019, financed by national funds through the FCT/MCTES and within the project POCI-01-0145-FEDER-031268 - funded by FEDER, through COMPETE2020 - Programa Operacional Competitividade e Internacionalização (POCI), and by national funds (OE), through FCT/MCTES. Mariah L. Toledo acknowledges University of São Paulo (Mobilidade internacional de duração 23especial). Ana P. M. Tavares acknowledges FCT for the Investigator Programme (IF/01634/2015). Matheus M. Pereira acknowledges the PhD grant (2740-13-3) and financial support from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Capes. João P. A. Silva acknowledges the support of FAPESP (Fundação de Amparo à Pesquisa do Estado de São Paulo-Process Number 2016/06683-0).pt_PT
dc.language.isoengpt_PT
dc.publisherACS Sustainable Chemistry & Engineeringpt_PT
dc.relationUID/CTM/50011/2019pt_PT
dc.relationPOCI-01-0145-FEDER-031268pt_PT
dc.relationIF/01634/2015pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectDeep eutectic solventspt_PT
dc.subjectEnzyme activitypt_PT
dc.subjectGreen solventspt_PT
dc.subjectLaccasept_PT
dc.subjectMolecular dockingpt_PT
dc.titleLaccase activation in deep eutectic solventspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage11806pt_PT
degois.publication.issue13pt_PT
degois.publication.lastPage11814pt_PT
degois.publication.titleACS Sustainable Chemistry & Engineeringpt_PT
degois.publication.volume7pt_PT
dc.date.embargo2020-04-01-
dc.relation.publisherversionAmerican Chemical Societypt_PT
dc.identifier.doi10.1021/acssuschemeng.9b02179pt_PT
dc.identifier.essn2168-0485pt_PT
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