随机突变提高单胺氧化酶活性

Increasing activity of a monoamine oxidase by random mutation

摘要:

前期获得了一个对底物美西律具有一定活性的单胺氧化酶突变体A-1 (F210V/L213C)。为进一步提高其酶活性，利用MegaWHOP PCR构建了库容约为104的随机突变库。筛选后获得了一个最优突变酶ep-1，比活力为A-1的189%。选择性测定结果表明，酶的对映体选择性有较大提高，E值由101提高到282；动力学常数测定揭示，酶催化效率有较大提高，kcat/Km由0.001 51 mmol/(L?s)提高到0.002 89 mmol/(L?s)。和A-1酶相比，在所测定的11种胺类底物中，ep-1对其他7种底物的比活力有较明显提高，对其他4种底物的比活力变化不大。序列分析表明，ep-1的突变为T162A。分子动力学模拟结果提示，该突变主要通过修正通道氨基酸的二级结构和扩大活性口袋来发挥作用。

关键词:单胺氧化酶，易错PCR，酶活力，分子动力学模拟

Abstract:

The monoamine oxidase mutant A-1 (F210V/L213C) from Aspergillus niger showed some catalytic activity on mexiletine. To futher improve its activity, the mutant was subjected to directed evolution with MegaWHOP PCR (Megaprimer PCR of Whole Plasmid) and selection employing a high-throughput agar plate-based colorimetric screen. This approach led to the identification of a mutant ep-1, which specific activity was 189% of that for A-1. The ep-1 also showed significantly improved enantioselectivity, with the E value increased from 101 to 282; its kinetic kcat/Km value increased from 0.001 51 mmol/(L?s) to 0.002 89 mmol/(L?s), suggesting that catalytic efficiency of ep-1 had been improved. The mutant showed obviously higher specific activities on 7 of all tested 11 amines substrates, and the others were comparable. Sequence analysis revealed that there was a new mutation T162A on ep-1. The molecular dynamics simulation indicated that T162A may affect the secondary structure of the substrate channel and expand the binding pocket.

Key words:monoamine oxidase, error-prone PCR, activity, molecular dynamics simulation