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The fed-batch principle for the molecular biology lab: controlled nutrient diets in ready-made media improve production of recombinant proteins in Escherichia coli

机译:分子生物学实验室的分批补料原理:在现成的培养基中控制营养饮食可改善大肠杆菌中重组蛋白的产生

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While the nutrient limited fed-batch technology is the standard of the cultivation of microorganisms and production of heterologous proteins in industry, despite its advantages in view of metabolic control and high cell density growth, shaken batch cultures are still the standard for protein production and expression screening in molecular biology and biochemistry laboratories. This is due to the difficulty and expenses to apply a controlled continuous glucose feed to shaken cultures. New ready-made growth media, e.g. by biocatalytic release of glucose from a polymer, offer a simple solution for the application of the fed-batch principle in shaken plate and flask cultures. Their wider use has shown that the controlled diet not only provides a solution to obtain significantly higher cell yields, but also in many cases folding of the target protein is improved by the applied lower growth rates; i.e. final volumetric yields for the active protein can be a multiple of what is obtained in complex medium cultures. The combination of the conventional optimization approaches with new and easy applicable growth systems has revolutionized recombinant protein production in Escherichia coli in view of product yield, culture robustness as well as significantly increased cell densities. This technical development establishes the basis for successful miniaturization and parallelization which is now an important tool for synthetic biology and protein engineering approaches. This review provides an overview of the recent developments, results and applications of advanced growth systems which use a controlled glucose release as substrate supply.
机译:营养有限的分批补料技术是工业中微生物培养和异源蛋白质生产的标准,尽管它在代谢控制和高细胞密度增长方面具有优势,但摇动分批培养仍是蛋白质生产和表达的标准。在分子生物学和生物化学实验室进行筛选。这是由于将受控的连续葡萄糖进料应用于摇动培养物的困难和费用。新的现成的增长媒体,例如通过生物催化从聚合物中释放葡萄糖,为将补料分批原理应用于摇板和烧瓶培养提供了简单的解决方案。它们的广泛使用表明,控制饮食不仅提供了一种获得明显更高的细胞产量的解决方案,而且在许多情况下,通过降低生长速度可以改善靶蛋白的折叠。即,活性蛋白的最终体积产量可以是在复杂培养基中获得的产量的倍数。鉴于产品产量,培养稳健性以及显着提高的细胞密度,传统优化方法与新型且易于应用的生长系统的结合彻底改变了大肠杆菌中重组蛋白的生产。这项技术发展为成功实现小型化和并行化奠定了基础,而现在它已成为合成生物学和蛋白质工程方法的重要工具。这篇综述概述了使用受控葡萄糖释放作为底物供应的先进生长系统的最新发展,结果和应用。

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