The enantioselective hydrolysis of racemic naproxen methyl ester in supercritical CO2 using Candida rugosa lipase

被引:18
作者
Salgin, Ugur [1 ]
Salgin, Sema
Takac, Serpil
机构
[1] Cumhuriyet Univ, Fac Engn, Dept Chem Engn, TR-58140 Sivas, Turkey
[2] Ankara Univ, Fac Engn, Dept Chem Engn, TR-06100 Ankara, Turkey
关键词
naproxen; racemic naproxen methyl ester; enantioselective hydrolysis; Candida rugosa lipase; supercritical CO2;
D O I
10.1016/j.supflu.2007.06.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The enantioselective hydrolysis of racemic naproxen methyl ester by Candida rugosa lipase (CRL) was studied in aqueous buffer solution/isooctane reaction system in the presence of supercritical CO2. The effects pressure (75-160 bar), temperature (32-42 degrees C ) and reaction time (0.5-12 h) on the enantiomeric excesses of the product (ee(p)) and the substrate (ee(s)), enantiomeric ratio (E), conversion (x) and enzyme activity were investigated in a batch reactor system. The highest enantiomeric ratio achieved at 120 bar of pressure, 37 C of temperature and 2 h of reaction time was E= 193 with x=41.3%, ee(p)=97.9% and ee(s)=68.8%. CRL remained active at least for 12h at 37 degrees C and 120 bar in supercritical CO2 medium. Furthermore. enantiomeric ratio increased with increasing reaction time and reached the value of E=236 with ee(p) =98.2%, ee(s) =70.0% and x=41.6% after 12 h of hydrolysis. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 316
页数:7
相关论文
共 40 条
[1]  
AAOLTEN O, 1999, CHEM SYNTHESIS USING, P414
[2]   Supercritical carbon dioxide as a reaction medium for enzymatic kinetic resolution of P-chiral hydroxymethanephosphinates [J].
Albrycht, M ;
Kielbasinski, P ;
Drabowicz, J ;
Mikolajczyk, M ;
Matsuda, T ;
Harada, T ;
Nakamura, K .
TETRAHEDRON-ASYMMETRY, 2005, 16 (11) :2015-2018
[3]   ENZYMATIC RESOLUTION OF (S)-(+)-NAPROXEN IN A CONTINUOUS REACTOR [J].
BATTISTEL, E ;
BIANCHI, D ;
CESTI, P ;
PINA, C .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (06) :659-664
[4]   High yield and optical purity in biocatalysed acylation of trans-2-phenyl-1-cyclohexanol with Candida rugosa lipase in non-conventional media [J].
Celia, EC ;
Cernia, E ;
D'Acquarica, I ;
Palocci, C ;
Soro, S .
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 1999, 6 (05) :495-503
[5]   QUANTITATIVE-ANALYSES OF BIOCHEMICAL KINETIC RESOLUTIONS OF ENANTIOMERS [J].
CHEN, CS ;
FUJIMOTO, Y ;
GIRDAUKAS, G ;
SIH, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (25) :7294-7299
[6]   A STRUCTURAL BASIS FOR THE CHIRAL PREFERENCES OF LIPASES [J].
CYGLER, M ;
GROCHULSKI, P ;
KAZLAUSKAS, RJ ;
SCHRAG, JD ;
BOUTHILLIER, F ;
RUBIN, B ;
SERREQI, AN ;
GUPTA, AK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (08) :3180-3186
[7]   Practical approaches to green solvents [J].
DeSimone, JM .
SCIENCE, 2002, 297 (5582) :799-803
[8]  
Drees M, 2002, EUR J ORG CHEM, V2002, P2405, DOI 10.1002/1099-0690(200207)2002:14<2405::AID-EJOC2405>3.0.CO
[9]  
2-1
[10]   EFFECT OF PRESSURE ON AN ENZYMATIC-REACTION IN A SUPERCRITICAL FLUID [J].
ERICKSON, JC ;
SCHYNS, P ;
COONEY, CL .
AICHE JOURNAL, 1990, 36 (02) :299-301