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首页> 外文期刊>BMC Biotechnology >Discovery and characterization of a highly efficient enantioselective mandelonitrile hydrolase from Burkholderia cenocepacia J2315 by phylogeny-based enzymatic substrate specificity prediction
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Discovery and characterization of a highly efficient enantioselective mandelonitrile hydrolase from Burkholderia cenocepacia J2315 by phylogeny-based enzymatic substrate specificity prediction

机译:通过基于系统进化的酶底物特异性预测发现和鉴定伯克霍尔德菌新陈代谢J2315的高效对映选择性扁桃腈水解酶

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Background A nitrilase-mediated pathway has significant advantages in the production of optically pure (R)-(?)-mandelic acid. However, unwanted byproduct, low enantioselectivity, and specific activity reduce its value in practical applications. An ideal nitrilase that can efficiently hydrolyze mandelonitrile to optically pure (R)-(?)-mandelic acid without the unwanted byproduct is needed. Results A novel nitrilase (BCJ2315) was discovered from Burkholderia cenocepacia J2315 through phylogeny-based enzymatic substrate specificity prediction (PESSP). This nitrilase is a mandelonitrile hydrolase that could efficiently hydrolyze mandelonitrile to (R)-(?)-mandelic acid, with a high enantiomeric excess of 98.4%. No byproduct was observed in this hydrolysis process. BCJ2315 showed the highest identity of 71% compared with other nitrilases in the amino acid sequence. BCJ2315 possessed the highest activity toward mandelonitrile and took mandelonitrile as the optimal substrate based on the analysis of substrate specificity. The kinetic parameters V max, K m, K cat, and K cat/ K m toward mandelonitrile were 45.4 μmol/min/mg, 0.14 mM, 15.4 s-1, and 1.1×105 M-1s-1, respectively. The recombinant Escherichia coli M15/BCJ2315 had a strong substrate tolerance and could completely hydrolyze mandelonitrile (100 mM) with fewer amounts of wet cells (10 mg/ml) within 1 h. Conclusions PESSP is an efficient method for discovering an ideal mandelonitrile hydrolase. BCJ2315 has high affinity and catalytic efficiency toward mandelonitrile. This nitrilase has great advantages in the production of optically pure (R)-(?)-mandelic acid because of its high activity and enantioselectivity, strong substrate tolerance, and having no unwanted byproduct. Thus, BCJ2315 has great potential in the practical production of optically pure (R)-(?)-mandelic acid in the industry.
机译:背景技术腈水解酶介导的途径在生产光学纯的(R)-(α)-扁桃酸中具有显着的优势。但是,不需要的副产物,低对映选择性和比活性降低了其在实际应用中的价值。需要一种理想的腈水解酶,其可以有效地将扁桃腈水解为光学纯的(R)-(β)-扁桃酸,而没有不需要的副产物。结果通过基于系统发育的酶底物特异性预测(PESSP),从新伯克霍尔德菌J2315中发现了一种新的腈水解酶(BCJ2315)。该腈水解酶是可以将扁桃腈有效地水解为(R)-(β)-扁桃酸的扁桃腈水解酶,对映体过量为98.4%。在该水解过程中未观察到副产物。与其他腈水解酶相比,BCJ2315在氨基酸序列中显示出最高的同一性71%。 BCJ2315对扁桃腈具有最高的活性,基于底物特异性的分析,以扁桃腈为最佳底物。动力学参数V max ,K m ,K cat 和K cat / K m < / sub>对扁桃腈为45.4μmol/ min / mg,0.14 mM,15.4 s -1 和1.1×10 5 M -1 s -1 。重组大肠杆菌M15 / BCJ2315具有很强的底物耐受性,并且可以在1 h内以较少量的湿细胞(10 mg / ml)完全水解扁桃腈(100 mM)。结论PESSP是发现理想的扁桃腈水解酶的有效方法。 BCJ2315对扁桃腈具有高亲和力和催化效率。该腈水解酶由于具有高活性和对映选择性,强的底物耐受性并且没有不需要的副产物而在光学纯的(R)-(α)-扁桃酸的生产中具有很大的优势。因此,BCJ2315在工业上实际生产光学纯的(R)-(α)-扁桃酸具有很大的潜力。

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