Srinivasan Sriram, Barnard Gavin C, Gerngross Tillman U
Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire 03755, USA.
Appl Environ Microbiol. 2002 Dec;68(12):5925-32. doi: 10.1128/AEM.68.12.5925-5932.2002.
We describe the development of a novel protein expression system based on the industrial fermentation organism Ralstonia eutropha (formerly known as Alcaligenes eutrophus) NCIMB 40124. This new system overcomes some of the shortcomings of traditional Escherichia coli-based protein expression systems, particularly the propensity of such systems to form inclusion bodies during high-level expression. Using a proteomics approach, we identified promoters that can be induced by simple process parameters or medium compositions in high-density cell culture or shake flasks, respectively. By combining newly developed molecular biological tools with a high-cell-density fermentation process, we were able to produce high levels (>1 g/liter) of soluble, active organophosphohydrolase, a model enzyme prone to inclusion body formation in E. coli.
我们描述了一种基于工业发酵微生物嗜中性产碱杆菌(以前称为真养产碱杆菌)NCIMB 40124开发的新型蛋白质表达系统。这个新系统克服了传统基于大肠杆菌的蛋白质表达系统的一些缺点,特别是这类系统在高水平表达时形成包涵体的倾向。通过蛋白质组学方法,我们分别鉴定出了可在高密度细胞培养或摇瓶中由简单工艺参数或培养基成分诱导的启动子。通过将新开发的分子生物学工具与高细胞密度发酵工艺相结合,我们能够生产出高水平(>1克/升)的可溶性、活性有机磷水解酶,这是一种在大肠杆菌中容易形成包涵体的模型酶。