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Ultrasensitive Reporter Protein Detection in Genetically Engineered Bacteria

机译:基因工程细菌中的超灵敏记者蛋白检测

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We demonstrate the use of laser-induced fluorescence confocal spectroscopy to measure analyte-stimulated enhanced green fluorescent protein (egfp) synthesis by genetically modified Escherichia coli bioreporter cells. Induction is measured in cell lysates and, since the spectroscopic focal volume is approximately the size of one bioreporter cell, also in individual live bacteria. This is, to our knowledge, the first ever proof-of-concept work utilizing instrumentation with single-molecule detection capability to monitor bioreporter response. Although we use arsenic inducible bioreporters here, the method is extensible to gfp/egfp bioreporters that are responsive to other substances.
机译:我们证明了使用激光诱导的荧光共聚焦光谱法来测量由基因修饰的大肠杆菌生物报告细胞对分析物刺激的增强型绿色荧光蛋白(egfp)的合成。诱导是在细胞裂解物中测量的,并且由于分光镜的焦点体积大约是一个生物报告细胞的大小,因此在单个活细菌中也是如此。据我们所知,这是有史以来首次概念验证工作,它利用具有单分子检测功能的仪器来监测生物报告者的反应。尽管我们在此使用砷诱导型生物报告物,但该方法可扩展至对其他物质有反应的gfp / egfp生物报告物。

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