铜绿假单胞菌反翻译特异性评价生物传感器的研制

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Bastien L’Hermitte, Thomas Chauvet, Sylvie Georgeault-Daguenet, Nicolas Le Yondre, Philippe Jehan, Reynald Gillet* and Christine Baysse*, 
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引用次数: 0

摘要

我们开发了两种铜绿假单胞菌生物传感器来检测这种医学相关病原体的反翻译抑制剂。这些生物传感器利用由原卟啉IX(铁螯合酶的底物)积累产生的红色荧光。第一个生物传感器监测tmrna - smpb介导的铁螯合酶的标记和降解,而第二个生物传感器通过跟踪clpp1介导的蛋白质水解和卟啉生物合成作为对照。在野生型和突变型背景下对这两种生物传感器进行了测试,并在微滴板上测量了相对于600 nm吸光度的红色荧光。结果证实了荧光与反翻译或蛋白质水解活性之间的联系。这些生物传感器为铜绿假单胞菌中反翻译抑制剂的高通量筛选提供了一个有前途的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Developing Biosensors for Specific Assessment of Trans-Translation in Pseudomonas aeruginosa

Developing Biosensors for Specific Assessment of Trans-Translation in Pseudomonas aeruginosa

We developed two Pseudomonas aeruginosa biosensors to detect trans-translation inhibitors in this medically relevant pathogen. These biosensors leverage the red fluorescence produced by the accumulation of protoporphyrin IX, the substrate of ferrochelatase. The first biosensor monitors tmRNA-SmpB-mediated tagging and degradation of ferrochelatase, while the second serves as a control by tracking ClpP1-mediated proteolysis and porphyrin biosynthesis. Both biosensors were tested in wild-type and mutant backgrounds, and red fluorescence was measured relative to absorbance at 600 nm in microtiter plates. The results confirmed a link between fluorescence and trans-translation or proteolysis activity. These biosensors offer a promising tool for high-throughput screening of trans-translation inhibitors in P. aeruginosa.

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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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