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Characterization of the all-E. coli transcription-translation system myTXTL by mass spectrometry.通过质谱法对全大肠杆菌转录-翻译系统myTXTL进行表征。
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Metabolomics Analysis of the Toxic Effects of the Production of Lycopene and Its Precursors.番茄红素及其前体物生产毒性效应的代谢组学分析
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Optimization of ClpXP activity and protein synthesis in an E. coli extract-based cell-free expression system.优化基于大肠杆菌提取物的无细胞表达系统中的 ClpXP 活性和蛋白质合成。
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In vitro transcription-translation using bacterial genome as a template to reconstitute intracellular profile.以细菌基因组为模板进行体外转录-翻译以重建细胞内概况。
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The E. coli S30 lysate proteome: A prototype for cell-free protein production.大肠杆菌 S30 无细胞提取物蛋白质组:无细胞蛋白生产的原型。
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Metabolic profiling by gas chromatography-mass spectrometry of energy metabolism in high-fat diet-fed obese mice.通过气相色谱-质谱联用技术对高脂饮食喂养的肥胖小鼠能量代谢进行代谢谱分析。
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用于工艺优化的无细胞表达系统的代谢谱分析

Metabolic Profiling of Cell-Free Expression Systems for Process Optimization.

作者信息

Miguez April M, McNerney Monica P, Styczynski Mark P

机构信息

School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, USA.

出版信息

Ind Eng Chem Res. 2019 Dec 18;58(50):22472-22482. doi: 10.1021/acs.iecr.9b03565. Epub 2019 Sep 13.

DOI:10.1021/acs.iecr.9b03565
PMID:32063671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7021278/
Abstract

Biotechnology has transformed the production of various chemicals and pharmaceuticals due to its efficient and selective processes, but it is inherently limited by its use of live cells as "biocatalysts." Cell-free expression (CFE) systems, which use a protein lysate isolated from whole cells, have the potential to overcome these challenges and broaden the scope of biomanufacturing. Implementation of CFE systems at scale will require determining clear markers of lysate activity and developing supplementation approaches that compensate for potential variability across batches and experimental protocols. Towards this goal, we use metabolomics to relate lysate preparation and performance to metabolic activity. We show that lysate processing affects the metabolite makeup of lysates, and that lysate metabolite levels change over the course of a CFE reaction regardless of whether a target compound is produced. Finally, we use this information to develop ways to standardize lysate activity and to design an improved CFE system.

摘要

生物技术因其高效且具选择性的过程,已改变了各种化学品和药物的生产,但它本质上受限于将活细胞用作“生物催化剂”。无细胞表达(CFE)系统使用从全细胞中分离出的蛋白质裂解物,有潜力克服这些挑战并拓宽生物制造的范围。大规模实施CFE系统将需要确定裂解物活性的明确标志物,并开发补偿批次间和实验方案潜在变异性的补充方法。为实现这一目标,我们使用代谢组学将裂解物制备和性能与代谢活性联系起来。我们表明,裂解物处理会影响裂解物的代谢物组成,并且无论是否产生目标化合物,裂解物代谢物水平在CFE反应过程中都会发生变化。最后,我们利用这些信息开发标准化裂解物活性的方法,并设计一种改进的CFE系统。