Cui Mingxin, Wong Okei, Shi Kexin, Li Qiang, Wang Wenya
Department of Chemical Engineering, Key Lab of Industrial Biocatalysis, Tsinghua University, Beijing 100084, China; College of Chemical Engineering, Qinghai University, Xining, Qinghai 810016, China.
Department of Chemical Engineering, Key Lab of Industrial Biocatalysis, Tsinghua University, Beijing 100084, China.
J Biotechnol. 2025 Feb;398:202-214. doi: 10.1016/j.jbiotec.2024.12.012. Epub 2025 Jan 6.
Efficient methods and universal DNA elements are eagerly required for the expression of proteins and the production of target chemicals in synthetic biology and metabolic engineering. This paper develops a customized-design approach by utilizing the host-independent T7 expression system (HITES), which facilitates the rational design and rapid construction of T7 expression systems. Firstly, the EL (Upper-limit value of initial enzyme activity) value is discovered to play a pivotal factor in the successful construction of the T7 expression system, different host strains exhibit varying EL values, and this study presents a method to measure the EL values. Secondly, E. coli DH5α is chosen as the host strain, and it demonstrates that various strategies to modulate T7 RNA polymerase activity can efficiently construct the HITES T7 expression system in E. coli DH5α under the guidance of EL. Lastly, the customized-design of HITES enables the efficient expression of sfGFP and D-MIase proteins across 13 host strains, guided by EL values. This customized-design method of HITES offers a streamlined pathway for T7 system construction across a broad range of hosts and serves as an enabling tool for synthetic biology, metabolic engineering, and enzyme engineering.
在合成生物学和代谢工程中,蛋白质表达和目标化学品生产急切需要高效方法和通用DNA元件。本文利用宿主独立的T7表达系统(HITES)开发了一种定制设计方法,该方法有助于T7表达系统的合理设计和快速构建。首先,发现EL(初始酶活性上限值)在T7表达系统的成功构建中起关键作用,不同宿主菌株表现出不同的EL值,本研究提出了一种测量EL值的方法。其次,选择大肠杆菌DH5α作为宿主菌株,结果表明,在EL的指导下,各种调节T7 RNA聚合酶活性的策略可以在大肠杆菌DH5α中高效构建HITES T7表达系统。最后,在EL值的指导下,HITES的定制设计能够在13种宿主菌株中高效表达sfGFP和D - MIase蛋白。HITES的这种定制设计方法为跨广泛宿主的T7系统构建提供了一条简化途径,并作为合成生物学、代谢工程和酶工程的有力工具。