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Enzyme-catalyzed resolution of racemate using enzyme functionalized silica nanoparticles in the presence of surfactants

Authors
Song, Yoon SeokLee, Hee UkLee, Jong HoPark, ChulhwanKim, Seung Wook
Issue Date
Mar-2011
Publisher
ELSEVIER SCI LTD
Keywords
Lipase; Resolution; Naproxen; Surfactant; Silica nanoparticle; Immobilization
Citation
PROCESS BIOCHEMISTRY, v.46, no.3, pp.817 - 820
Indexed
SCIE
SCOPUS
Journal Title
PROCESS BIOCHEMISTRY
Volume
46
Number
3
Start Page
817
End Page
820
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/113031
DOI
10.1016/j.procbio.2010.12.010
ISSN
1359-5113
Abstract
The enzyme-catalyzed resolution of racemic naproxen 2,2,2-trifluoroethyl thioester was performed by the immobilization of lipase on silica nanoparticles using a covalent bonding method. To increase the conversion and reaction rate of this resolution, we investigated the effect of non-ionic surfactants (M-SA 1025 and SM 20). The optimal reaction conditions such as temperature and loading amount of immobilized lipase were also determined. The addition of M-SA 1025 resulted in the increase in reaction rate (V-S), conversion (X-S) and enantioselectivity (E value) comparison with SM 20 and the control. The reaction performed in a mixture containing M-SA 1025 at 50 degrees C with 80 U/mL of immobilized lipase markedly improved the resolution of racemic naproxen 2,2,2-trifluoroethyl thioester compared to other conditions. (C) 2010 Elsevier Ltd. All rights reserved.
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