Department of Pathophysiology, Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education, Shanghai Jiao-Tong University School of Medicine (SJTU-SM), Shanghai 200025, China.
Abiochem Co. LTD, Shanghai, China.
Sci Rep. 2017 Feb 6;7:42064. doi: 10.1038/srep42064.
Halohydrin dehalogenases (HHDHs) are biocatalytically interesting enzymes due to their ability to form C-C, C-N, C-O, and C-S bonds. One of most important application of HHDH was the protein engineering of HheC (halohydrin dehalogenase from Agrobacterium radiobacter AD1) for the industrial manufacturing of ethyl (R)-4-cyano-3-hydroxybutanoate (HN), a key chiral synthon of a cholesterol-lowering drug of atorvastatin. During our development of an alternative, more efficient and economic route for chemo-enzymatic preparation of the intermediate of atorvastatin, we found that the HheC2360 previously reported for HN manufacture, had insufficient activity for the cyanolysis production of tert-butyl (3 R,5 S)-6-cyano-3,5-dihydroxyhexanoate (A7). Herein, we present the focused directed evolution of HheC2360 with higher activity and enhanced biocatalytic performance using active site mutagenesis. Through docking of the product, A7, into the crystal structure of HheC2360, 6 residues was selected for combined active sites testing (CASTing). After library screening, the variant V84G/W86F was identified to have a 15- fold increase in activity. Time course analysis of the cyanolysis reaction catalyzed by this variant, showed 2- fold increase in space time productivity compared with HheC2360. These results demonstrate the applicability of the variant V84G/W86F as a biocatalyst for the efficient and practical production of atorvastatin intermediate.
卤代醇脱卤酶(HHDHs)具有形成 C-C、C-N、C-O 和 C-S 键的能力,因此是具有生物催化意义的酶。HHDH 的最重要应用之一是对 HheC(来自根瘤农杆菌 AD1 的卤代醇脱卤酶)进行蛋白质工程改造,用于工业制造手性药物阿托伐他汀的关键手性前体(R)-4-氰基-3-羟基丁酸乙酯(HN)。在开发阿托伐他汀中间体化学酶法制备的替代、更高效和经济路线的过程中,我们发现之前报道的用于 HN 制造的 HheC2360 对于叔丁基(3R,5S)-6-氰基-3,5-二羟基己酸酯(A7)的氰解生产活性不足。在此,我们通过定点定向进化,利用活性位点诱变提高 HheC2360 的活性和增强生物催化性能。通过将产物 A7 对接至 HheC2360 的晶体结构,选择 6 个残基进行组合活性位点测试(CASTing)。经过文库筛选,确定 V84G/W86F 变体的活性提高了 15 倍。该变体催化的氰解反应的时程分析表明,与 HheC2360 相比,时空产率提高了 2 倍。这些结果证明变体 V84G/W86F 可作为生物催化剂用于高效实用地生产阿托伐他汀中间体。