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用于蛋白质生产和合成生物学的集成无细胞代谢平台。

An integrated cell-free metabolic platform for protein production and synthetic biology.

作者信息

Jewett Michael C, Calhoun Kara A, Voloshin Alexei, Wuu Jessica J, Swartz James R

机构信息

Department of Chemical Engineering, Stanford University, Stanford, CA 94305-5025, USA.

出版信息

Mol Syst Biol. 2008;4:220. doi: 10.1038/msb.2008.57. Epub 2008 Oct 14.

Abstract

Cell-free systems offer a unique platform for expanding the capabilities of natural biological systems for useful purposes, i.e. synthetic biology. They reduce complexity, remove structural barriers, and do not require the maintenance of cell viability. Cell-free systems, however, have been limited by their inability to co-activate multiple biochemical networks in a single integrated platform. Here, we report the assessment of biochemical reactions in an Escherichia coli cell-free platform designed to activate natural metabolism, the Cytomim system. We reveal that central catabolism, oxidative phosphorylation, and protein synthesis can be co-activated in a single reaction system. Never before have these complex systems been shown to be simultaneously activated without living cells. The Cytomim system therefore promises to provide the metabolic foundation for diverse ab initio cell-free synthetic biology projects. In addition, we describe an improved Cytomim system with enhanced protein synthesis yields (up to 1200 mg/l in 2 h) and lower costs to facilitate production of protein therapeutics and biochemicals that are difficult to make in vivo because of their toxicity, complexity, or unusual cofactor requirements.

摘要

无细胞系统为拓展天然生物系统用于有益目的(即合成生物学)的能力提供了一个独特的平台。它们降低了复杂性,消除了结构障碍,并且不需要维持细胞活力。然而,无细胞系统一直受到其无法在单个集成平台中共同激活多个生化网络的限制。在此,我们报告了在一个旨在激活天然代谢的大肠杆菌无细胞平台(即细胞模拟系统)中对生化反应的评估。我们发现,中心分解代谢、氧化磷酸化和蛋白质合成可以在单个反应系统中共同激活。此前从未有过这些复杂系统在无活细胞的情况下被证明能同时激活的报道。因此,细胞模拟系统有望为各种从头开始的无细胞合成生物学项目提供代谢基础。此外,我们描述了一种改进的细胞模拟系统,其蛋白质合成产量更高(2小时内可达1200毫克/升)且成本更低,便于生产因毒性、复杂性或特殊辅因子需求而难以在体内制造的蛋白质治疗剂和生化物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d18b/2583083/c0917bfca1e4/msb200857-f1.jpg

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