Miguez April M, McNerney Monica P, Styczynski Mark P
School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, USA.
Ind Eng Chem Res. 2019 Dec 18;58(50):22472-22482. doi: 10.1021/acs.iecr.9b03565. Epub 2019 Sep 13.
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.
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。