Mihovilovic Marko D, Rudroff Florian, Winninger Alexander, Schneider Toni, Schulz Frank, Reetz Manfred T
Vienna University of Technology, Institute of Applied Synthetic Chemistry, Getreidemarkt 9/163-OC, A-1060 Vienna, Austria.
Org Lett. 2006 Mar 16;8(6):1221-4. doi: 10.1021/ol0601040.
[reaction: see text] An array of random mutants of cyclohexanone monooxygenase (CHMO) from Acinetobacter sp. NCIMB 9871 was screened against a library of structurally diverse ketones for modifications in the substrate acceptance profile and stereopreference of the enzymatic Baeyer-Villiger biooxidation. While the set of mutant biocatalysts was initially evolved for the enantiocomplementary oxidation of 4-hydroxycyclohexanone, improved and/or divergent stereoselectivities were observed for several substrates. In addition, expanded substrate acceptance to facilitate biotransformation of sterically demanding ketones was found.
[反应:见正文] 针对一系列结构多样的酮类文库,筛选了不动杆菌属NCIMB 9871中环己酮单加氧酶(CHMO)的随机突变体阵列,以研究酶促拜耳-维利格生物氧化反应中底物接受谱和立体选择性的变化。虽然最初开发这组突变生物催化剂是用于4-羟基环己酮的对映互补氧化反应,但对几种底物观察到了提高的和/或不同的立体选择性。此外,还发现扩大了底物接受范围,以促进空间位阻较大的酮的生物转化。