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Enhancing the catalytic potential of nitrilase from Pseudomonas putida for stereoselective nitrile hydrolysis

机译:增强恶臭假单胞菌腈水解酶催化立体选择性腈水解的能力

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摘要

(R)-mandelic acid was produced from racemic mandelonitrile using free and immobilized cells of Pseudomonas putida MTCC 5110 harbouring a stereoselective nitrilase. In addition to the optimization of culture conditions and medium components, an inducer feeding approach is suggested to achieve enhanced enzyme production and therefore higher degree of conversion of mandelonitrile. The relationship between cell growth periodicity and enzyme accumulation was also studied, and the addition of the inducer was delayed by 6 h to achieve maximum nitrilase activity. The nitrilase expression was also authenticated by the sodium dodecyl phosphate-polyacrylamide gel electrophoresis analysis. P. putida MTCC 5110 cells were further immobilized in calcium alginate, and the immobilized biocatalyst preparation was used for the enantioselective hydrolysis of mandelonitrile. The immobilized system was characterized based on the Thiele modulus (ϕ). Efficient biocatalyst recycling was achieved as a result of immobilization with immobilized cells exhibiting 88% conversion even after 20 batch recycles. Finally, a fed batch reaction was set up on a preparative scale to produce 1.95 g of (R)-(-)-mandelic acid with an enantiomeric excess of 98.8%.
机译:(R)-扁桃酸是由外消旋扁桃腈使用含有立体选择性腈水解酶的恶臭假单胞菌MTCC 5110的游离和固定化细胞产生的。除了优化培养条件和培养基成分外,还建议采用诱导剂补料方法,以提高酶的产量,从而提高扁桃腈的转化率。还研究了细胞生长周期与酶积累之间的关系,并且诱导剂的添加延迟了6小时以实现最大的腈水解酶活性。通过磷酸十二烷基钠-聚丙烯酰胺凝胶电泳也可以验证腈水解酶的表达。将恶臭假单胞菌MTCC 5110细胞进一步固定在藻酸钙中,并将固定的生物催化剂制剂用于扁桃腈的对映选择性水解。固定化的系统基于Thiele模量(ϕ)进行表征。固定化细胞的固定化结果实现了有效的生物催化剂循环利用,即使在20次分批回收之后,固定化细胞仍显示出88%的转化率。最后,以制备规模建立补料分批反应,以产生1.95g对映体过量为98.8%的(R)-(-)-扁桃酸。

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  • 来源
    《Applied Microbiology and Biotechnology 》 |2006年第1期| 77-87| 共11页
  • 作者单位

    Department of Pharmaceutical Technology (Biotechnology) National Institute of Pharmaceutical Education and Research Sector-67;

    Department of Pharmaceutical Technology (Biotechnology) National Institute of Pharmaceutical Education and Research Sector-67;

    Department of Pharmaceutical Technology (Biotechnology) National Institute of Pharmaceutical Education and Research Sector-67;

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