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http://acervodigital.unesp.br/handle/11449/111697
- Title:
- Easily handling penicillin G acylase magnetic cross-linked enzymes aggregates: Catalytic and morphological studies
- Universidade Federal de São Carlos (UFSCar)
- Universidade Estadual Paulista (UNESP)
- 1359-5113
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- 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.
- 1-Jan-2014
- Process Biochemistry. Oxford: Elsevier Sci Ltd, v. 49, n. 1, p. 38-46, 2014.
- 38-46
- Elsevier B.V.
- Cross-linked enzymes aggregates
- Superparamagnetic nanoparticles
- Supramolecular complex
- Magnetic recovery of enzymes
- Penicillin hydrolysis
- http://dx.doi.org/10.1016/j.procbio.2013.09.024
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/111697
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