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利用重组大肠杆菌生产腈酶的响应面法。

Response surface methodology of nitrilase production by recombinant Escherichia coli.

机构信息

Biocatalysis Laboratory, Department of Pharmaceutical Technology, National Institute of Pharmaceutical Education and Research , Sector 67, S.A.S. Nagar-160 062, Punjab , India ; School of Pharmaceutical Sciences, University of Geneva & University of Lausanne , 30 Quai Ernest Ansermet, 1211 Geneva , Switzerland.

出版信息

Braz J Microbiol. 2011 Jul;42(3):1085-92. doi: 10.1590/S1517-838220110003000029. Epub 2011 Sep 1.

Abstract

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.

摘要

利用响应面法对携带 pET 21(b) 质粒的重组大肠杆菌细胞进行生长和腈水解酶生产,以表达恶臭假单胞菌腈水解酶。采用中心组合设计获得关键培养基成分的理想浓度,包括果糖、胰蛋白胨、酵母提取物和乳糖。发现果糖、胰蛋白胨、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)。在这里,果糖作为细胞生长的碳源,而乳糖则优选作为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,而胰蛋白胨则作为主要氮源添加。使用这种优化的培养基,实验得到的生长值(600nm 处的 OD 值)为 6.67,腈水解酶活性为 27.13 U/ml。与未优化的培养基相比,这种培养基开发方法分别使生长和酶活性提高了 1.4 倍和 2.2 倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f7/3768802/33e26cb4479a/bjm-43-1085-g001.jpg

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