A Robust and Orthogonal Far-Red Light Sensor for Gene Expression Control in Escherichia coli.

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2025-05-16 Epub Date: 2025-05-06 DOI:10.1021/acssynbio.5c00044
Yueyang Sun, Mengran Xu, Baiyang Wang, Chenyang Xia, Zhiming He, Bowen Lu, Jiyun Cui, Qiancheng Liao, Qi Xu, Fei Gan
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引用次数: 0

Abstract

Optogenetics has emerged as a powerful tool for regulating cellular processes due to its noninvasive nature and precise spatiotemporal control. Far-red light (FRL) has increasingly been used in the optogenetic control of mammalian cells due to its low toxicity and high tissue penetration. However, robust and orthogonal FRL sensors are lacking in bacteria. Here, we established an orthogonal FRL sensor in Escherichia coli with a maximum dynamic range exceeding 230-fold based on the RfpA-RfpC-RfpB (RfpABC) signaling system that regulates the far-red light photoacclimation (FaRLiP) in cyanobacteria. We identified a conserved DNA motif in the promoter sequences of the Chl f synthase gene and other genes in the FaRLiP gene clusters, termed the far-red light-regulatory (FLR) motif, which enables the light-responsive activation of gene expression through its interaction with RfpB. Based on the FLR motif, we simplified the FLR-containing promoters and characterized their activation abilities and dynamic ranges, which can be utilized in different synthetic biology scenarios. Additionally, one or two FLR motifs are present at other loci within the FaRLiP gene cluster, providing further FRL-inducible promoter resources. The FRL sensor exhibits effective activation and suppression under low-intensity FRL and white light, respectively, and remains functional in darkness. In conclusion, this study advances the understanding of the regulatory mechanisms of FaRLiP in cyanobacteria and provides robust and orthogonal FRL sensors for synthetic biology applications.

用于大肠杆菌基因表达控制的鲁棒正交远红光传感器。
光遗传学由于其非侵入性和精确的时空控制而成为调控细胞过程的有力工具。远红光因其低毒性和高组织穿透性而越来越多地用于哺乳动物细胞的光遗传控制。然而,在细菌中缺乏可靠的正交FRL传感器。本研究基于调控蓝藻远红光光驯化(FaRLiP)的RfpA-RfpC-RfpB (RfpABC)信号系统,在大肠杆菌中建立了最大动态范围超过230倍的正交FRL传感器。我们在Chl f合成酶基因的启动子序列和FaRLiP基因簇中的其他基因中发现了一个保守的DNA基序,称为远红光调控(FLR)基序,它通过与RfpB的相互作用使基因表达的光响应激活。基于FLR基序,我们对含有FLR的启动子进行了简化,并对其激活能力和动态范围进行了表征,使其能够应用于不同的合成生物学场景。此外,在FaRLiP基因簇的其他位点上存在一个或两个FLR基序,提供了进一步的frl诱导启动子资源。FRL传感器在低强度FRL和白光下分别表现出有效的激活和抑制,并在黑暗中保持功能。总之,本研究促进了对蓝藻中FaRLiP调控机制的理解,并为合成生物学应用提供了强大的正交FRL传感器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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