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dc.contributor.authorCruz Izquierdo, Álvaro
dc.contributor.authorPicó, Enrique A.
dc.contributor.authorLópez, Carmen
dc.contributor.authorSerra Ferrer, Juan Luis
dc.contributor.authorLlama Fontal, María Jesús
dc.date.accessioned2015-09-25T12:30:24Z
dc.date.available2015-09-25T12:30:24Z
dc.date.issued2014-12-31
dc.identifier.citationPLOS ONE 9 (12) : (2014) // Article ID 25551445es
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/15686
dc.description.abstractEnzyme-catalyzed production of biodiesel is the object of extensive research due to the global shortage of fossil fuels and increased environmental concerns. Herein we report the preparation and main characteristics of a novel biocatalyst consisting of Cross-Linked Enzyme Aggregates (CLEAs) of Candida antarctica lipase B (CALB) which are covalently bound to magnetic nanoparticles, and tackle its use for the synthesis of biodiesel from non-edible vegetable and waste frying oils. For this purpose, insolubilized CALB was covalently cross-linked to magnetic nanoparticles of magnetite which the surface was functionalized with –NH2 groups. The resulting biocatalyst combines the relevant catalytic properties of CLEAs (as great stability and feasibility for their reutilization) and the magnetic character, and thus the final product (mCLEAs) are superparamagnetic particles of a robust catalyst which is more stable than the free enzyme, easily recoverable from the reaction medium and reusable for new catalytic cycles. We have studied the main properties of this biocatalyst and we have assessed its utility to catalyze transesterification reactions to obtain biodiesel from non-edible vegetable oils including unrefined soybean, jatropha and cameline, as well as waste frying oil. Using 1% mCLEAs (w/w of oil) conversions near 80% were routinely obtained at 30°C after 24 h of reaction, this value rising to 92% after 72 h. Moreover, the magnetic biocatalyst can be easily recovered from the reaction mixture and reused for at least ten consecutive cycles of 24 h without apparent loss of activity. The obtained results suggest that mCLEAs prepared from CALB can become a powerful biocatalyst for application at industrial scale with better performance than those currently available.es
dc.description.sponsorshipThis work was supported by grants from the University of the Basque Country (UPV/EHU, project GIU11/25 and scholarship for AC-I, http://www.ehu.es), the Spanish Ministry of Economy and Competitiveness (project CTQ2011-25052, http://www.mineco.es), the Basque Government (project SAIOTEK S-PE12UN041, http://www.euskadi.net), Ikerbasque, the Basque Foundation for Science (fellowship for CL, www.ikerbasque.net) and European Union (project Energreen, POCTEFA EFA217/11, http://www.poctefa.eu/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es
dc.language.isoenges
dc.publisherPublic Library Sciencees
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectiron-oxide nanoparticleses
dc.subjectFE3O4 nanoparticleses
dc.subjectimmobilized lipasees
dc.subjectcatalyzed transesterificationes
dc.subjectenantioselective hydrolysises
dc.subjectcovalent immobilizationes
dc.subjectpotential applicationses
dc.subjectperformancees
dc.subjectCLEAses
dc.subjectstabilizationes
dc.titleMagnetic Cross-Linked Enzyme Aggregates (mCLEAs) of Candida antarctica Lipase: An Efficient and Stable Biocatalyst for Biodiesel Synthesises
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2014 Cruz-Izquierdo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.relation.publisherversionhttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0115202es
dc.identifier.doi10.1371/journal.pone.0115202
dc.departamentoesBioquímica y biología moleculares_ES
dc.departamentoeuBiokimika eta biologia molekularraes_ES
dc.subject.categoriaMEDICINE
dc.subject.categoriaBIOCHEMISTRY AND MOLECULAR BIOLOGY
dc.subject.categoriaAGRICULTURAL AND BIOLOGICAL SCIENCES


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