Heiss C, Laivenieks M, Zeikus J G, Phillips R S
Department of Chemistry and Molecular Biology, University of Georgia, Athens, GA 30602-2556, USA.
Bioorg Med Chem. 2001 Jul;9(7):1659-66. doi: 10.1016/s0968-0896(01)00073-6.
The mutation of Cys-295 to alanine in Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase (SADH) was performed to give C295A SADH, on the basis of molecular modeling studies utilizing the X-ray crystal structure coordinates of the highly homologous T. brockii secondary alcohol dehydrogenase (1YKF.PDB). This mutant SADH has activity for 2-propanol comparable to wild-type SADH. However, the C295A mutation was found to cause a significant shift of enantioselectivity toward the (S)-configuration in the reduction of some ethynylketones to the corresponding chiral propargyl alcohols. This result confirms our prediction that Cys-295 is part of a small alkyl group binding pocket whose size determines the binding orientation of ketone substrates, and, hence, the stereochemical configuration of the product alcohol. Furthermore, C295A SADH has much higher activity towards t-butyl and some alpha-branched ketones than does wild-type SADH. The C295A mutation does not affect the thioester reductase activity of SADH. The broader substrate specificity and altered stereoselectivity for C295A SADH make it a potentially useful tool for asymmetric reductions.
基于利用高度同源的嗜热栖热菌二级醇脱氢酶(1YKF.PDB)的X射线晶体结构坐标进行的分子建模研究,将嗜热栖热菌二级醇脱氢酶(SADH)中的半胱氨酸-295突变为丙氨酸,得到C295A SADH。这种突变型SADH对2-丙醇的活性与野生型SADH相当。然而,发现C295A突变在将一些乙炔基酮还原为相应的手性炔丙醇时,导致对映选择性显著向(S)-构型转变。这一结果证实了我们的预测,即半胱氨酸-295是一个小烷基结合口袋的一部分,其大小决定了酮底物的结合方向,从而决定了产物醇的立体化学构型。此外,C295A SADH对叔丁基酮和一些α-支链酮的活性比野生型SADH高得多。C295A突变不影响SADH的硫酯还原酶活性。C295A SADH更广泛的底物特异性和改变的立体选择性使其成为不对称还原的潜在有用工具。