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Simple defined autoinduction medium for high-level recombinant protein production using T7-based Escherichia coli expression systems.

机译:使用基于T7的大肠杆菌表达系统进行高水平重组蛋白生产的简单定义的自动诱导培养基。

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摘要

Protein production under the control of lac operon regulatory elements using autoinduction is based on diauxic growth of Escherichia coli on lactose after consumption of more preferred carbon substrates. A novel simple and cost-effective defined autoinduction medium using a mixture of glucose, glycerol, and lactose as carbon substrate and NH(4)(+) as sole nitrogen source without any supplementation of amino acids and vitamins was developed for T7-based E. coli expression systems. This medium was successfully employed in 96-well microtiter plates, test tubes, shake flasks, and 15-L bioreactor cultivations for production of different types of proteins achieving an average yield of 500 mg L(-1) product. Cell-specific protein concentrations and solubility were similar as during conventional isopropyl β-D-1-thiogalactopyranoside induction using Luria-Bertani broth. However, the final yield of target proteins was about four times higher, as a higher final biomass was achieved using this novel defined autoinduction broth.
机译:使用自动诱导在lac操纵子调控元件控制下的蛋白质生产是基于消耗了更多优选碳底物后大肠杆菌在乳糖上的双生生长。针对基于T7的E,开发了一种新颖,简单且具有成本效益的自动感应培养基,该培养基使用葡萄糖,甘油和乳糖的混合物作为碳底物,而NH(4)(+)作为唯一的氮源,不添加任何氨基酸和维生素。大肠杆菌表达系统。该培养基已成功用于96孔微量滴定板,试管,摇瓶和15 L生物反应器培养物中,用于生产不同类型的蛋白质,平均产量为500 mg L(-1)。细胞特异性蛋白浓度和溶解度与使用Luria-Bertani肉汤诱导常规异丙基β-D-1-硫代吡喃半乳糖苷相似。但是,靶蛋白的最终产量要高出约四倍,因为使用这种新颖的自动诱导培养液可获得更高的最终生物量。

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