Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19802
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dc.contributor.authorde Souza, Ranyere Lucenapt
dc.contributor.authorPache de Faria, Emanuelle Limapt
dc.contributor.authorFigueiredo, Renan Tavarespt
dc.contributor.authorFreitas, Lisiane dos Santospt
dc.contributor.authorIglesias, Miguelpt
dc.contributor.authorMattedi, Silvanapt
dc.contributor.authorZanin, Gisella Mariapt
dc.contributor.authorAndreo dos Santos, Onelia Aparecidapt
dc.contributor.authorCoutinho, Joao A. P.pt
dc.contributor.authorLima, Alvaro Silvapt
dc.contributor.authorFaria Soares, Cleide Marapt
dc.date.accessioned2017-12-07T19:25:20Z-
dc.date.issued2013pt
dc.identifier.issn0141-0229pt
dc.identifier.urihttp://hdl.handle.net/10773/19802-
dc.description.abstractIonic liquids (ILs) have evolved as a new type of non-aqueous solvents for biocatalysis, mainly due to their unique and tunable physical properties. A number of recent review papers have described a variety of enzymatic reactions conducted in IL solutions, on the other hand, to improve the enzyme's activity and stability in ILs; major methods being explored include the enzyme immobilization (on solid support, sol-gel, etc.), protic ionic liquids used as an additive process. The immobilization of the lipase from Burkholderia cepacia by the sol-gel technique using protic ionic liquids (PIL) as additives to protect against inactivation of the lipase due to release of alcohol and shrinkage of the gel during the sol-gel process was investigated in this study. The influence of various factors such as the length of the alkyl chain of protic ionic liquids (monoethanolamine-based) and a concentration range between 0.5 and 3.0% (w/v) were evaluated. The resulting hydrophobic matrices and immobilized lipases were characterised with regard to specific surface area, adsorption-desorption isotherms, pore volume (V-p) and size (d(p)) according to nitrogen adsorption and scanning electron microscopy (SEM), physico-chemical properties (thermogravimetric - TG, differential scanning calorimetry - DSC and Fourier transform infrared spectroscopy - FTIR) and the potential for ethyl ester and emulsifier production. The total activity yields (Y-a) for matrices of immobilized lipase employing protic ionic liquids as additives always resulted in higher values compared with the sample absent the protic ionic liquids, which represents 35-fold increase in recovery of enzymatic activity using the more hydrophobic protic ionic liquids. Compared with arrays of the immobilized biocatalyst without additive, in general, the immobilized biocatalyst in the presence of protic ionic liquids showed increased values of surface area (143-245 m(2) g(-1)) and pore size (19-38 angstrom). Immobilization with protic ionic liquids also favoured reduced mass loss according to TG curves (always less than 42.9%) when compared to the immobilized matrix without protic ionic liquids (45.1%), except for the sample containing 3.0% protic ionic liquids (46.5%), verified by thermogravimetric analysis. Ionic liquids containing a more hydrophobic alkyl group in the cationic moiety were beneficial for recovery of the activity of the immobilized lipase. The physico-chemical characterization confirmed the presence of the enzyme and its immobilized derivatives obtained in this study by identifying the presence of amino groups, and profiling enthalpy changes of mass loss. (c) 2013 Elsevier Inc. All rights reserved.pt
dc.language.isoengpt
dc.publisherELSEVIER SCIENCE INCpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.rightsrestrictedAccesspor
dc.subjectREVERSIBLE IMMOBILIZATIONpt
dc.subjectCOVALENT IMMOBILIZATIONpt
dc.subjectCEPACIA LIPASEpt
dc.subjectCANDIDA-RUGOSApt
dc.subjectSURFACE-AREApt
dc.subjectSOYBEAN OILpt
dc.subjectADSORPTIONpt
dc.subjectBIODIESELpt
dc.subjectGALACTOSIDASEpt
dc.subjectBIOCATALYSTpt
dc.titleProtic ionic liquid as additive on lipase immobilization using silica sol-gelpt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage141pt
degois.publication.issue3pt
degois.publication.lastPage150pt
degois.publication.titleENZYME AND MICROBIAL TECHNOLOGYpt
degois.publication.volume52pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1016/j.enzmictec.2012.12.007pt
dc.identifier.doi10.1016/j.enzmictec.2012.12.007pt
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