Enantioselective Esterification of Ibuprofen under Microwave Irradiation
AbstractEnantioselective esterification of ibuprofen has been successfully carried out in an organic solvent catalyzed by recombinant APE 1547 (a thermophilic esterase from the archaeon Aeropyrum pernix K1). Here we used microwave irradiation (MW) as the mode of heating to improve the enzyme performance. Under the optimum conditions, the enzyme activity of APE 1547 was 4.16 μmol/mg/h and the enantioselectivity (E value) was 52.9. Compared with conventional heating, the enzyme activity and the enantioselectivity were increased about 21.9-fold and 1.4-fold, respectively. The results also indicated that APE 1547 can maintain 95% of its activity even after being used five times, suggesting that the enzyme is stable under low power MW conditions.
Scifeed alert for new publicationsNever miss any articles matching your research from any publisher
- Get alerts for new papers matching your research
- Find out the new papers from selected authors
- Updated daily for 49'000+ journals and 6000+ publishers
- Define your Scifeed now
Yang, Z.; Niu, X.; Fang, X.; Chen, G.; Zhang, H.; Yue, H.; Wang, L.; Zhao, D.; Wang, Z. Enantioselective Esterification of Ibuprofen under Microwave Irradiation. Molecules 2013, 18, 5472-5481.
Yang Z, Niu X, Fang X, Chen G, Zhang H, Yue H, Wang L, Zhao D, Wang Z. Enantioselective Esterification of Ibuprofen under Microwave Irradiation. Molecules. 2013; 18(5):5472-5481.Chicago/Turabian Style
Yang, Zecheng; Niu, Xuedun; Fang, Xuedong; Chen, Ge; Zhang, Hong; Yue, Hong; Wang, Lei; Zhao, Dantong; Wang, Zhi. 2013. "Enantioselective Esterification of Ibuprofen under Microwave Irradiation." Molecules 18, no. 5: 5472-5481.