Yadav Surendra, Perkins Alexander J P, Liyanagedera Sahan B W, Bougas Anthony, Laohakunakorn Nadanai
Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, U.K.
ACS Synth Biol. 2025 Jan 17;14(1):247-256. doi: 10.1021/acssynbio.4c00697. Epub 2025 Jan 4.
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 . 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.
“利用重组元件进行蛋白质合成”(“PURE”)系统是一种最小生化系统,能够使用特定的酶组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、乙酸激酶和过氧化氢酶的ATP再生系统对PURE进行了扩展。新途径从丙酮酸、磷酸盐和氧气生成乙酰磷酸,用于使ATP重新磷酸化。成功的ATP再生需要约10 mM磷酸盐缓冲液的高初始浓度,令人惊讶的是,这并不影响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中现有的基于肌酸的系统联合使用;联合系统可产生高达233 μg/mL的mCherry,与单独使用肌酸系统相比提高了78%。这些结果在多批自制的PURE中具有可重复性,重要的是也适用于商业系统,如新英格兰生物实验室的PURExpress。这些结果展示了一种合理的自下而上的方法来改造PURE,为无细胞合成生物学和合成细胞构建中的应用铺平了道路。