Improving the catalytic activity of formate dehydrogenase from Candida boidinii by using magnetic nanoparticles
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
01/11/2013
01/11/2013
2012
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Resumo |
Formate dehydrogenase from Candida boidinii (FDH) was immobilized on three different magnetic supports: one composed by magnetite nanoparticles directly silanized with ARTS (aminopropyltriethoxysilane), i.e. MagNP-APTS: the second one containing a silica gel coated magnetite core which was further silanized with APTS (MagNP@SiO2-APTS), and the third one consisting of magnetite-APTS coated with Glyoxyl-Agarose (MagNP-Glyoxyl-Agarose). The catalytic activity of the three FDH systems was investigated as a function of pH and temperature. The silica gel coated nanoparticles provided the highest conversion rates; however, in terms of recycling, magnetite without the silica shell led to the most stable system. By using the enzyme tryptophan residues as internal fluorescence probes, the structure-activity behavior was investigated in the presence of the formate and NAD(+) substrates, revealing a rather contrasting behavior in the three cases. Because of its peculiar behavior, a direct interaction of the magnetic nanoparticles with the catalytic sites seems to be implicated in the case of MagNP-APTS. (C) 2012 Elsevier B.V. All rights reserved. |
Identificador |
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, AMSTERDAM, v. 84, n. 4, pp. 136-143, DEC, 2012 1381-1177 http://www.producao.usp.br/handle/BDPI/37395 10.1016/j.molcatb.2012.03.021 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE BV AMSTERDAM |
Relação |
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC |
Direitos |
closedAccess Copyright ELSEVIER SCIENCE BV |
Palavras-Chave | #FORMATE DEHYDROGENASE #IMMOBILIZATION #MAGNETIC NANOPARTICLES #TRYPTOPHAN FLUORESCENCE #IMMOBILIZATION #MECHANISMS #CONVERSION #GEL #BIOCHEMISTRY & MOLECULAR BIOLOGY #CHEMISTRY, PHYSICAL |
Tipo |
article Proceedings Paper publishedVersion |