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Response surface methodology of nitrilase production by recombinant Escherichia coli

机译:重组大肠杆菌生产腈水解酶的响应面方法

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摘要

Growth and nitrilase production by recombinant Escherichia coli cells harbouring pET 21 (b) plasmid, for the expression of Pseudomonas putida nitrilase were improved using response surface methodology. Central composite design was used for obtaining ideal concentration of critical medium components which include fructose, tryptone, yeast extract and lactose. The optimal values for the concentration of fructose, tryptone, yeast extract and lactose were found to be 1.13, 2.26, 3.25 and 0.9 % (w/v), respectively. Here, fructose served as carbon source for the growth while lactose was preferably used as inducer for the expression of foreign protein. Yeast extract in the medium was used as a growth promoter while tryptone was added as a major nitrogen source. Using this optimized medium, an experimental growth of 6.67 (OD at 600 nm) and nitrilase activity of 27.13 U/ml was achieved. This approach for medium development led to an enhancement of the growth and enzyme activity by 1.4 and 2.2 times, respectively, as compared to the un-optimized medium.
机译:使用响应表面方法改善了带有pET 21(b)质粒的重组大肠杆菌细胞的生长和腈水解酶的生产,用于表达恶臭假单胞菌腈水解酶。中央复合设计用于获得关键培养基成分(包括果糖,胰蛋白,、酵母提取物和乳糖)的理想浓度。发现果糖,胰蛋白,、酵母提取物和乳糖的最佳浓度分别为1.13、2.26、3.25和0.9%(w / v)。在此,果糖用作生长的碳源,而乳糖优选用作外源蛋白表达的诱导剂。培养基中的酵母提取物用作生长促进剂,而胰蛋白tone则作为主要的氮源。使用这种优化的培养基,实现了6.67(OD在600 nm处)的实验生长和27.13 U / ml的腈水解酶活性。与未优化的培养基相比,这种培养基培养方法分别使生长和酶活性提高了1.4倍和2.2倍。

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