设计热休克反应最小的抗热基因控制装置

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2024-09-20 Epub Date: 2024-08-16 DOI:10.1021/acssynbio.4c00236
Haofeng Chen, Shan Jiang, Kaixuan Xu, Ziyu Ding, Jiangkai Wang, Mingfeng Cao, Jifeng Yuan
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引用次数: 0

摘要

由于温度是一种通用的输入信号,热休克基因控制在重组蛋白质生产和代谢工程应用中获得了极大的关注。传统的恒温系统通常需要持续暴露于热刺激下才能触发目标基因的长时间表达,而伴随而来的热休克反应对生物生产过程不利。在本研究中,我们设计了热休克法定量感应(ThermoQS)电路,使大肠杆菌记录瞬时热刺激。通过将输入的热量转化为法定量感应分子(如从铜绿假单胞菌中提取的酰基高丝氨酸内酯)的积累,在最小的热刺激下实现了持续的基因表达。此外,我们还证明,我们对大肠杆菌 Lac 操作子进行了重新编程,使其对热刺激做出了反应,信噪比(S/N)达到了令人印象深刻的 15.3。综上所述,我们认为本研究中报告的 ThermoQS 系统有望显著降低未来代谢工程应用的设计和实验成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design of Thermoresponsive Genetic Controls with Minimal Heat-Shock Response.

Design of Thermoresponsive Genetic Controls with Minimal Heat-Shock Response.

As temperature serves as a versatile input signal, thermoresponsive genetic controls have gained significant interest for recombinant protein production and metabolic engineering applications. The conventional thermoresponsive systems normally require the continuous exposure of heat stimuli to trigger the prolonged expression of targeted genes, and the accompanied heat-shock response is detrimental to the bioproduction process. In this study, we present the design of thermoresponsive quorum-sensing (ThermoQS) circuits to make Escherichia coli record transient heat stimuli. By conversion of the heat input into the accumulation of quorum-sensing molecules such as acyl-homoserine lactone derived from Pseudomonas aeruginosa, sustained gene expressions were achieved by a minimal heat stimulus. Moreover, we also demonstrated that we reprogrammed the E. coli Lac operon to make it respond to heat stimuli with an impressive signal-to-noise ratio (S/N) of 15.3. Taken together, we envision that the ThermoQS systems reported in this study are expected to remarkably diminish both design and experimental expenditures for future metabolic engineering applications.

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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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