Establishing a High-Yield Bacillus subtilis-Based Cell-Free Protein Synthesis System for In Vitro Prototyping and Natural Product Biosynthesis

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Xiangyang Ji, Wan-Qiu Liu, Zhiling Cao, Shuhui Huang and Jian Li*, 
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Abstract

Cell-free systems are emerging as powerful platforms for synthetic biology with widespread applications in both fundamental research, such as artificial cell construction, and practical uses like recombinant protein production. Among these, cell-free protein synthesis (CFPS) plays a crucial role in gene expression for various downstream applications. However, the development of CFPS systems based on certain chassis, such as Bacillus subtilis, still remains limited due to their low in vitro productivity. Here, we report the development of a highly productive CFPS system derived from an engineered B. subtilis 164T7P strain, which contains a genomic integration of the T7 RNA polymerase gene. This modification allows the preparation of cell extracts that inherently contain T7 RNA polymerase, enabling T7 promoter-based transcription without the supplementation of purified T7 RNA polymerase in CFPS reactions. Through systematic optimization of cell extract preparation and key reaction parameters, we achieved the synthesis of 286 ± 16.7 μg/mL of sfGFP in batch reactions, with yields increasing to over 1100 μg/mL in a semicontinuous format that can replenish substrates and remove inhibitory byproducts. We further demonstrated the system’s versatility by using it for two synthetic biology applications: prototyping ribosome binding site (RBS) elements and synthesizing pulcherriminic acid─a bioactive cyclodipeptide. The system successfully characterized RBS performance, with in vitro and in vivo rankings correlating with predicted strengths, and expressed two active biosynthetic enzymes (cyclodipeptide synthase─YvmC and cytochrome P450 enzyme─CypX), leading to the production of pulcherriminic acid. Overall, our B. subtilis-based CFPS system offers a robust platform for high-yield protein synthesis, in vitro prototyping of gene regulatory elements, and natural product biosynthesis, highlighting its broad potential for synthetic biology and biotechnology applications.

Abstract Image

无细胞系统正在成为合成生物学的强大平台,广泛应用于人工细胞构建等基础研究和重组蛋白生产等实际用途。其中,无细胞蛋白质合成(CFPS)在各种下游应用的基因表达中发挥着至关重要的作用。然而,基于某些底盘(如枯草芽孢杆菌)的无细胞蛋白质合成系统的发展仍然受到限制,因为它们的体外生产率较低。在这里,我们报告了一种高生产率 CFPS 系统的开发情况,该系统来源于经改造的枯草芽孢杆菌 164T7P 菌株,其中包含 T7 RNA 聚合酶基因的基因组整合。这种改造允许制备本身就含有 T7 RNA 聚合酶的细胞提取物,从而实现基于 T7 启动子的转录,而无需在 CFPS 反应中补充纯化的 T7 RNA 聚合酶。通过对细胞提取物制备和关键反应参数进行系统优化,我们在批量反应中合成了 286 ± 16.7 μg/mL sfGFP,在可补充底物和去除抑制性副产物的半连续形式下,产量增至 1100 μg/mL 以上。我们将该系统用于两种合成生物学应用,进一步证明了它的多功能性:核糖体结合位点(RBS)元件原型和合成 pulcherriminic acid(一种具有生物活性的环二肽)。该系统成功鉴定了核糖体结合位点的性能,体外和体内排名与预测强度相关,并表达了两种活性生物合成酶(环二肽合成酶─YvmC 和细胞色素 P450 酶─CypX),从而产生了 pulcherriminic 酸。总之,我们基于枯草芽孢杆菌的 CFPS 系统为高产蛋白质合成、基因调控元件体外原型设计和天然产物生物合成提供了一个强大的平台,凸显了其在合成生物学和生物技术应用方面的广泛潜力。
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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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