Easily handling penicillin G acylase magnetic cross-linked enzymes aggregates: Catalytic and morphological studies

dc.contributor.authorKopp, Willian
dc.contributor.authorCosta, Taciane P. da [UNESP]
dc.contributor.authorPereira, Sandra C.
dc.contributor.authorJafelicci, Miguel [UNESP]
dc.contributor.authorGiordano, Roberto C. [UNESP]
dc.contributor.authorMarques, Rodrigo Fernando Costa [UNESP]
dc.contributor.authorAraujo-Moreira, Fernando M.
dc.contributor.authorGiordano, Raquel L. C.
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:08:54Z
dc.date.available2014-12-03T13:08:54Z
dc.date.issued2014-01-01
dc.description.abstractBiomolecules labeled with superparamagnetic nanoparticles can be selectively removed from complex reaction mixtures using an external magnetic field. Amino-functionalized superparamagnetic iron oxide nanoparticles (amino-SPION) were co-aggregated with penicillin G acylase and then cross-linked, generating magnetic cross-linked enzymes aggregates (M-CLEAs) that were quickly and efficiently recovered from the reaction medium by applying an external magnetic field. M-CLEAs and cross-linked enzymes aggregates (CLEAs) prepared under the same reaction conditions were characterized and compared. The best recovered activities were obtained for M-CLEAs prepared using polyethylene glycol 600 as precipitant and the most stable M-CLEA were obtained using tert-butanol. Successive penicillin G hydrolysis reactions were carried out using the same M-CLEA in a 50 mL reactor (3 reaction cycles), after the reactions the derivate was magnetically recovered without loss of activity demonstrating a total magnetic recovery. Line-scan energy dispersive X-ray spectroscopy showed that the amino-SPIONs were homogeneously dispersed within the structure of the M-CLEA. (C) 2013 Elsevier Ltd. All rights reserved.en
dc.description.affiliationFed Univ Silo Carlos UFSCar, Dept Chem Engn, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationUNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationFed Univ Silo Carlos UFSCar, Dept Phys, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent38-46
dc.identifierhttp://dx.doi.org/10.1016/j.procbio.2013.09.024
dc.identifier.citationProcess Biochemistry. Oxford: Elsevier Sci Ltd, v. 49, n. 1, p. 38-46, 2014.
dc.identifier.doi10.1016/j.procbio.2013.09.024
dc.identifier.issn1359-5113
dc.identifier.lattes2115942621694174
dc.identifier.orcid0000-0003-0195-3885
dc.identifier.urihttp://hdl.handle.net/11449/111697
dc.identifier.wosWOS:000331156100006
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofProcess Biochemistry
dc.relation.ispartofjcr2.616
dc.relation.ispartofsjr0,761
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectCross-linked enzymes aggregatesen
dc.subjectSuperparamagnetic nanoparticlesen
dc.subjectSupramolecular complexen
dc.subjectMagnetic recovery of enzymesen
dc.subjectPenicillin hydrolysisen
dc.titleEasily handling penicillin G acylase magnetic cross-linked enzymes aggregates: Catalytic and morphological studiesen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.lattes2115942621694174[6]
unesp.author.orcid0000-0003-0195-3885[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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