ATP Regeneration from Pyruvate in the PURE System.

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2025-01-17 Epub Date: 2025-01-04 DOI:10.1021/acssynbio.4c00697
Surendra Yadav, Alexander J P Perkins, Sahan B W Liyanagedera, Anthony Bougas, Nadanai Laohakunakorn
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Abstract

The "Protein synthesis Using Recombinant Elements" ("PURE") system is a minimal biochemical system capable of carrying out cell-free protein synthesis using defined enzymatic components. This study extends PURE by integrating an ATP regeneration system based on pyruvate oxidase, acetate kinase, and catalase. The new pathway generates acetyl phosphate from pyruvate, phosphate, and oxygen, which is used to rephosphorylate ATP in situ. Successful ATP regeneration requires a high initial concentration of ∼10 mM phosphate buffer, which surprisingly does not affect the protein synthesis activity of PURE. The pathway can function independently or in combination with the existing creatine-based system in PURE; the combined system produces up to 233 μg/mL of mCherry, an enhancement of 78% compared to using the creatine system alone. The results are reproducible across multiple batches of homemade PURE and importantly also generalize to commercial systems such as PURExpress from New England Biolabs. These results demonstrate a rational bottom-up approach to engineering PURE, paving the way for applications in cell-free synthetic biology and synthetic cell construction.

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丙酮酸在PURE系统中的ATP再生。
“使用重组元素合成蛋白质”(“PURE”)系统是一个最小的生化系统,能够使用特定的酶成分进行无细胞蛋白质合成。本研究通过整合基于丙酮酸氧化酶、醋酸激酶和过氧化氢酶的ATP再生系统扩展了PURE。新途径由丙酮酸、磷酸盐和氧生成乙酰磷酸,用于原位再磷酸化ATP。成功的ATP再生需要高初始浓度的~ 10 mM磷酸盐缓冲液,令人惊讶的是,这不会影响PURE的蛋白质合成活性。该途径可以独立发挥作用,也可以与PURE中现有的肌酸系统结合;联合系统产生高达233 μg/mL的mCherry,与单独使用肌酸系统相比,提高了78%。结果可在多批次自制PURE中重现,重要的是也可推广到商业系统,如新英格兰生物实验室的pureexpress。这些结果证明了一种合理的自下而上的方法来设计PURE,为无细胞合成生物学和合成细胞构建的应用铺平了道路。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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