Easily handling penicillin G acylase magnetic cross-linked enzymes aggregates: Catalytic and morphological studies
dc.contributor.author | Kopp, Willian | |
dc.contributor.author | Costa, Taciane P. da [UNESP] | |
dc.contributor.author | Pereira, Sandra C. | |
dc.contributor.author | Jafelicci, Miguel [UNESP] | |
dc.contributor.author | Giordano, Roberto C. [UNESP] | |
dc.contributor.author | Marques, Rodrigo Fernando Costa [UNESP] | |
dc.contributor.author | Araujo-Moreira, Fernando M. | |
dc.contributor.author | Giordano, Raquel L. C. | |
dc.contributor.institution | Universidade Federal de São Carlos (UFSCar) | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-12-03T13:08:54Z | |
dc.date.available | 2014-12-03T13:08:54Z | |
dc.date.issued | 2014-01-01 | |
dc.description.abstract | Biomolecules 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.affiliation | Fed Univ Silo Carlos UFSCar, Dept Chem Engn, BR-13565905 Sao Carlos, SP, Brazil | |
dc.description.affiliation | UNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil | |
dc.description.affiliation | Fed Univ Silo Carlos UFSCar, Dept Phys, BR-13565905 Sao Carlos, SP, Brazil | |
dc.description.affiliationUnesp | UNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.format.extent | 38-46 | |
dc.identifier | http://dx.doi.org/10.1016/j.procbio.2013.09.024 | |
dc.identifier.citation | Process Biochemistry. Oxford: Elsevier Sci Ltd, v. 49, n. 1, p. 38-46, 2014. | |
dc.identifier.doi | 10.1016/j.procbio.2013.09.024 | |
dc.identifier.issn | 1359-5113 | |
dc.identifier.lattes | 2115942621694174 | |
dc.identifier.orcid | 0000-0003-0195-3885 | |
dc.identifier.uri | http://hdl.handle.net/11449/111697 | |
dc.identifier.wos | WOS:000331156100006 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Process Biochemistry | |
dc.relation.ispartofjcr | 2.616 | |
dc.relation.ispartofsjr | 0,761 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | Cross-linked enzymes aggregates | en |
dc.subject | Superparamagnetic nanoparticles | en |
dc.subject | Supramolecular complex | en |
dc.subject | Magnetic recovery of enzymes | en |
dc.subject | Penicillin hydrolysis | en |
dc.title | Easily handling penicillin G acylase magnetic cross-linked enzymes aggregates: Catalytic and morphological studies | en |
dc.type | Artigo | |
dcterms.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dcterms.rightsHolder | Elsevier B.V. | |
unesp.author.lattes | 2115942621694174[6] | |
unesp.author.orcid | 0000-0003-0195-3885[6] | |
unesp.campus | Universidade Estadual Paulista (Unesp), Instituto de Química, Araraquara | pt |
unesp.department | Físico-Química - IQAR | pt |