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首页> 外文期刊>Journal of Biotechnology >Recombinant gene expression in Escherichia coli cultivation using lactoseas inducer
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Recombinant gene expression in Escherichia coli cultivation using lactoseas inducer

机译:使用乳糖酶诱导剂重组基因表达在大肠杆菌培养中

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摘要

The use of lactose as inducer of foreign gene expression under control of the lac UV5 promoter was investigated in recombinant Escherichia coli. Chicken muscle troponin C (TnC) gene was transcripted by T7 RNA polymerase and expressed in bioreactor cultivations after a feed-forward controlled fed-batch growth phase. Cell concentrations of 22 g(-1) dry cell weight (DCW)-before induction starred-were used to achieve a TnC content of 19.5% of total cell protein through an induction strategy that combined the addition of a specific lactose amount of 4.7 g g(-1) DCW divided into three pulses and the addition of yeast extract (1 g1(-1)) together with the second and the third lactose pulses. The results presented suggest that the residual lactose concentration play:; an important role on the production of the heterologous protein.
机译:在重组大肠杆菌中研究了在Rac uV5启动子控制下的外源基因表达的诱导剂的使用。 鸡肉肌肉肌钙蛋白C(TNC)基因被T7 RNA聚合酶转录,并在前馈控制的批量生产阶段后在生物反应器培养中表达。 22g(-1)干细胞重量(DCW)的细胞浓度 - 通过诱导策略来实现通过诱导策略来实现19.5%的总细胞蛋白的TNC含量,所述致策略组合添加4.7gg的特定乳糖量 (-1)DCW分为三个脉冲,并将酵母提取物(1g1(-1))与第二和第三乳糖脉冲一起添加。 提出的结果表明,残留的乳糖浓度起作用: 关于异源蛋白质的产生重要作用。

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