Zhang Hua Yun, Wang Xin, Ching Chi Bun
Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore 117576.
Chirality. 2007 May 5;19(4):245-9. doi: 10.1002/chir.20347.
Immobilized lipase from Candida antarctica (Novozym 435) was employed in the kinetic resolution of racemic flurbiprofen by enantioselective esterification with methanol. It was found that the lipase has the R-stereopreference and the reaction matches Bi Bi Ping Pong mechanism with dead-end inhibition of methanol. Furthermore, the R-stereopreference was analyzed in details from the aspects of enzymatic kinetic mechanism and reaction activation energy of both enantiomers. The R-enantiomer shows lower activation energy and higher maximum reaction rate than the S-enantiomer, which implies the R-stereopreference of the lipase and makes the kinetic resolution of flurbiprofen via enzymatic reaction feasible.
利用南极假丝酵母固定化脂肪酶(诺维信435),通过与甲醇进行对映选择性酯化反应,对外消旋氟比洛芬进行动力学拆分。研究发现,该脂肪酶具有R-立体选择性,且反应符合双底物双产物乒乓机制,并存在甲醇的终产物抑制作用。此外,从酶促动力学机制和两种对映体的反应活化能方面,对R-立体选择性进行了详细分析。R-对映体比S-对映体表现出更低的活化能和更高的最大反应速率,这表明了脂肪酶的R-立体选择性,使得通过酶促反应对氟比洛芬进行动力学拆分成为可能。