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通过改变生长培养基来激活能量代谢,使无细胞表达能够实现 24 小时工作流程。

Activation of Energy Metabolism through Growth Media Reformulation Enables a 24-Hour Workflow for Cell-Free Expression.

机构信息

Department of Biological Sciences, California Polytechnic State University, San Luis Obispo, California 93407, United States.

Center for Application in Biotechnology, California Polytechnic State University, San Luis Obispo, California 93407, United States.

出版信息

ACS Synth Biol. 2020 Oct 16;9(10):2765-2774. doi: 10.1021/acssynbio.0c00283. Epub 2020 Sep 14.

Abstract

Cell-free protein synthesis (CFPS) platforms have undergone numerous workflow improvements to enable diverse applications in research, biomanufacturing, and education. The cell extract-based platform has been broadly adopted due to its affordability and versatility. The upstream processing of cells to generate crude cell lysate remains time-intensive and technically nuanced, representing one of the largest sources of cost associated with the biotechnology. To overcome these limitations, we have improved the processes by developing a long-lasting autoinduction media formulation for CFPS that obviates human intervention between inoculation and harvest. The cell-free autoinduction (CFAI) media supports the production of robust cell extracts from high cell density cultures nearing the stationary phase of growth. As a result, the total mass of cells and the resulting extract volume obtained increases by 400% while maintaining robust reaction yields of reporter protein, sfGFP (>1 mg/mL). Notably, the CFAI workflow allows users to go from cells on a streak plate to completing CFPS reactions within 24 h. The CFAI workflow uniquely enabled us to elucidate the metabolic limits in CFPS associated with cells grown to stationary phase in the traditional 2× YTPG media. Metabolomics analysis demonstrates that CFAI-based extracts overcome these limits due to improved energy metabolism and redox balance. The advances reported here shed new light on the metabolism associated with highly active CFPS reactions and inform future efforts to tune the metabolism in CFPS systems. Additionally, we anticipate that the improvements in the time and cost-efficiency of CFPS will increase the simplicity and reproducibility, reducing the barriers for new researchers interested in implementing CFPS.

摘要

无细胞蛋白质合成 (CFPS) 平台经历了多次工作流程改进,使其能够在研究、生物制造和教育等多个领域得到广泛应用。由于其成本效益和多功能性,基于细胞提取物的平台得到了广泛采用。为了生成粗细胞裂解物,对细胞进行上游处理仍然需要耗费大量时间,并且技术上也很复杂,这是与生物技术相关的最大成本之一。为了克服这些限制,我们通过开发一种用于 CFPS 的长效自动诱导培养基配方来改进这些过程,该配方省去了接种和收获之间的人工干预。无细胞自动诱导 (CFAI) 培养基支持从接近生长静止期的高密度培养物中生产出强大的细胞提取物。因此,细胞总质量和获得的提取物体积增加了 400%,同时保持了报告蛋白 sfGFP(>1mg/mL)的稳健反应产率。值得注意的是,CFAI 工作流程允许用户从划线平板上的细胞在 24 小时内完成 CFPS 反应。CFAI 工作流程独特地使我们能够阐明与在传统 2×YTPG 培养基中生长到静止期的细胞相关的 CFPS 中的代谢限制。代谢组学分析表明,基于 CFAI 的提取物克服了这些限制,因为它们改善了能量代谢和氧化还原平衡。这里报道的进展为与高活性 CFPS 反应相关的代谢提供了新的认识,并为未来在 CFPS 系统中调整代谢的努力提供了信息。此外,我们预计 CFPS 在时间和成本效率方面的改进将提高其简单性和可重复性,降低对有兴趣实施 CFPS 的新研究人员的障碍。

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