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CRISPR干扰小RNA:嗜铁素还原地杆菌胞外电子传递的转录-翻译调控

CRISPRi-sRNA: Transcriptional-Translational Regulation of Extracellular Electron Transfer in Shewanella oneidensis.

作者信息

Cao Yingxiu, Li Xiaofei, Li Feng, Song Hao

机构信息

Key Laboratory of Systems Bioengineering (Ministry of Education), SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), School of Chemical Engineering and Technology, Tianjin University , Tianjin 300350, P.R. China.

出版信息

ACS Synth Biol. 2017 Sep 15;6(9):1679-1690. doi: 10.1021/acssynbio.6b00374. Epub 2017 Jun 15.

Abstract

Extracellular electron transfer (EET) in Shewanella oneidensis MR-1, which is one of the most well-studied exoelectrogens, underlies many microbial electrocatalysis processes, including microbial fuel cells, microbial electrolysis cells, and microbial electrosynthesis. However, regulating the efficiency of EET remains challenging due to the lack of efficient genome regulation tools that regulate gene expression levels in S. oneidensis. Here, we systematically established a transcriptional regulation technology, i.e., clustered regularly interspaced short palindromic repeats interference (CRISPRi), in S. oneidensis MR-1 using green fluorescent protein (GFP) as a reporter. We used this CRISPRi technology to repress the expression levels of target genes, individually and in combination, in the EET pathways (e.g., the MtrCAB pathway and genes affecting the formation of electroactive biofilms in S. oneidensis), which in turn enabled the efficient regulation of EET efficiency. We then established a translational regulation technology, i.e., Hfq-dependent small regulatory RNA (sRNA), in S. oneidensis by repressing the GFP reporter and mtrA, which is a critical gene in the EET pathways in S. oneidensis. To achieve coordinated transcriptional and translational regulation at the genomic level, the CRISPRi and Hfq-dependent sRNA systems were incorporated into a single plasmid harbored in a recombinant S. oneidensis strain, which enabled an even higher efficiency of mtrA gene repression in the EET pathways than that achieved by the CRISPRi and Hfq-dependent sRNA system alone, as exhibited by the reduced electricity output. Overall, we developed a combined CRISPRi-sRNA method that enabled the synergistic transcriptional and translational regulation of target genes in S. oneidensis. This technology involving CRISPRi-sRNA transcriptional-translational regulation of gene expression at the genomic level could be applied to other microorganisms.

摘要

嗜铁还原地杆菌MR-1是研究最为深入的产电微生物之一,其胞外电子传递(EET)是许多微生物电催化过程的基础,这些过程包括微生物燃料电池、微生物电解池和微生物电合成。然而,由于缺乏能调控嗜铁还原地杆菌基因表达水平的高效基因组调控工具,调控EET效率仍然具有挑战性。在此,我们以绿色荧光蛋白(GFP)作为报告基因,在嗜铁还原地杆菌MR-1中系统地建立了一种转录调控技术,即成簇规律间隔短回文重复序列干扰(CRISPRi)。我们利用这种CRISPRi技术单独或组合抑制EET途径(如嗜铁还原地杆菌中的MtrCAB途径和影响电活性生物膜形成的基因)中靶基因的表达水平,进而实现了对EET效率的有效调控。然后,我们通过抑制GFP报告基因和mtrA(嗜铁还原地杆菌EET途径中的关键基因),在嗜铁还原地杆菌中建立了一种翻译调控技术,即Hfq依赖性小调节RNA(sRNA)。为了在基因组水平实现转录和翻译的协同调控,将CRISPRi和Hfq依赖性sRNA系统整合到一个重组嗜铁还原地杆菌菌株携带的单个质粒中,与单独的CRISPRi和Hfq依赖性sRNA系统相比,这使得EET途径中mtrA基因的抑制效率更高,如电力输出降低所示。总体而言,我们开发了一种联合CRISPRi-sRNA方法,该方法能够对嗜铁还原地杆菌中的靶基因进行协同转录和翻译调控。这种涉及在基因组水平对基因表达进行CRISPRi-sRNA转录-翻译调控的技术可应用于其他微生物。

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