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首页> 外文期刊>ACS Synthetic Biology >The All E-coli TX-TL Toolbox 2.0: A Platform for Cell-Free Synthetic Biology
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The All E-coli TX-TL Toolbox 2.0: A Platform for Cell-Free Synthetic Biology

机译:全E-大肠杆菌TX-TL工具箱2.0:无细胞合成生物学平台

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摘要

We report on and provide a detailed characterization of the performance and properties of a recently developed, all Escherichia coli, cell-free transcription and translation system. Gene expression is entirely based on the endogenous translation components and transcription machinery provided by an E. coli cytoplasmic extract, thus expanding the repertoire of regulatory parts to hundreds of elements. We use a powerful metabolism for ATP regeneration to achieve more than 2 mg/mL of protein synthesis in batch mode reactions, and more than 6 mg/mL in semicontinuous mode. While the strength of cell-free expression is increased by a factor of 3 on average, the output signal of simple gene circuits and the synthesis of entire bacteriophages are increased by orders of magnitude compared to previous results. Messenger RNAs and protein degradation, respectively tuned using E. coli MazF interferase and ClpXP AAA+ proteases, are characterized over a much wider range of rates than the first version of the cell-free toolbox This system is a highly versatile cell-free platform to construct complex biological systems through the execution of DNA programs composed of synthetic and natural bacterial regulatory parts.
机译:我们报告并提供最新开发的,全大肠杆菌,无细胞转录和翻译系统的性能和特性的详细表征。基因表达完全基于大肠杆菌胞质提取物提供的内源性翻译成分和转录机制,从而将调节部分的范围扩展到数百个元件。我们使用强大的新陈代谢来进行ATP再生,以分批模式进行的蛋白质合成超过2 mg / mL,而以半连续模式进行的蛋白质合成超过6 mg / mL。尽管无细胞表达的强度平均提高了3倍,但与以前的结果相比,简单基因电路的输出信号和整个噬菌体的合成都增加了几个数量级。与第一版无细胞工具箱相比,分别使用大肠杆菌MazF干扰酶和ClpXP AAA +蛋白酶调节的信使RNA和蛋白质降解具有更高的速率范围。该系统是构建高度灵活的无细胞平台通过执行由合成和天然细菌调控部分组成的DNA程序来实现复杂的生物系统。

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