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Cloning, overexpression and biocatalytic exploration of a novel baeyer-villiger monooxygenase from ASPERGILLUS FUMIGATUS AF293

机译:一种新的来自ASPERGILLUS FUMIGATUS AF293的拜尔-维利格单加氧酶的克隆,过表达和生物催化探索

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摘要

The presence of several putative Baeyer-Villiger Monooxygenases (BVMOs) encoding genes in Aspergillus fumigatus Af293 was demonstrated for the first time. One of the identified BVMO-encoding genes was cloned and successfully overexpressed fused to the cofactor regenerating enzyme phosphite dehydrogenase (PTDH). The enzyme named BVMOAf1 was extensively characterized in terms of its substrate scope and essential kinetic features. It showed high chemo-, regio- and stereoselectivity not only in the oxidation of asymmetric sulfides, (S)-sulfoxides were obtained with 99% ee, but also in the kinetic resolution of bicyclo[3.2.0]hept-2-en-6-one. This kinetic resolution process led to the production of (1S,5R) normal lactone and (1R,5S) abnormal lactone with a regioisomeric ratio of 1:1 and 99% ee each. Besides, different reaction conditions, such as pH, temperature and the presence of organic solvents, have been tested, revealing that BVMOAf1 is a relatively robust biocatalyst.
机译:首次证明在烟曲霉Af293中存在几种假定的Baeyer-Villiger单加氧酶(BVMOs)编码基因。克隆了一个已鉴定的BVMO编码基因,并成功地过表达与辅因子再生亚磷酸酯脱氢酶(PTDH)融合。酶名为BVMOAf1的底物范围和基本动力学特征得到了广泛表征。它不仅在不对称硫化物的氧化中表现出高的化学,区域和立体选择性,还以99%ee获得了(S)-亚砜,而且在双环[3.2.0] hept-2-en-的动力学分辨率上也如此。 6一此动力学拆分过程导致产生(1S,5R)正常内酯和(1R,5S)异常内酯,其区域异构体比率分别为1:1和99%ee。此外,已经测试了不同的反应条件,例如pH,温度和有机溶剂的存在,这表明BVMOAf1是一种相对坚固的生物催化剂。

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