Castillo Betzaida, Delgado Yamixa, Barletta Gabriel, Griebenow Kai
Department of Chemistry, University of Puerto Rico, Río Piedras Campus, P.O. Box 23346, San Juan, Puerto Rico 00931-3346.
Tetrahedron. 2010 Mar 20;66(12):2175-2180. doi: 10.1016/j.tet.2010.01.053.
Enzyme catalysis in organic solvents is a powerful tool for stereo-selective synthesis but the enantioselectivity is still hard to predict. To overcome this obstacle, we employed a nanoparticulate formulation of subtilisin Carlsberg (SC) and designed a series of 14 structurally related racemic alcohols. They were employed in the model transesterification reaction with vinyl butyrate and the enantioselectivities were determined. In general, short alcohol side chains led to low enantioselectivties, while larger and bulky side chains caused better discrimination of the enantiomers by the enzyme. With several bulky substrates high enantioselectivities with E>100 were obtained. Computational modeling highlighted that key to high enantioselectivity is the discrimination of the R and S substrates by the sole hydrophobic binding pocket based on their size and bulkiness. While bulky S enantiomer side chains could be accommodated within the binding pocket, bulky R enantiomer side chains could not. However, when also the S enantiomer side chain becomes too large and does not fit into the binding pocket anymore, enantioselectivity accordingly drops.
有机溶剂中的酶催化是立体选择性合成的有力工具,但对映选择性仍然难以预测。为了克服这一障碍,我们采用了卡尔伯格枯草杆菌蛋白酶(SC)的纳米颗粒制剂,并设计了一系列14种结构相关的外消旋醇。将它们用于与丁酸乙烯酯的模型酯交换反应中,并测定了对映选择性。一般来说,短的醇侧链导致低对映选择性,而较大且 bulky 的侧链使酶对映体的区分效果更好。对于几种 bulky 底物,获得了 E>100 的高对映选择性。计算模型强调,高对映选择性的关键是基于尺寸和体积,通过唯一的疏水结合口袋区分 R 和 S 底物。虽然 bulky 的 S 对映体侧链可以容纳在结合口袋中,但 bulky 的 R 对映体侧链则不能。然而,当 S 对映体侧链也变得太大而不再适合结合口袋时,对映选择性相应下降。