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Fluorescence and bioluminescence reporter functions in genetically modified bacterial sensor strains

机译:转基因细菌传感器菌株中的荧光和生物发光报告基因功能

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摘要

Genetically modified bacteria, engineered to generate a quantifiable signal in response to pre-determined sets of environmental conditions, may serve as combined sensing/reporting elements in whole-cell biosensors. We have compared two of the several available reporter genes in such cells: green fluorescent proteins (GFPs) (Aquorea victoria gfp) and bioluminescence (Vibrio fischeri luxCDABE) genes, fused to either SOS (recA) or heat shock (grpE) promoters. In both cases, bacterial bioluminescence allowed faster and more sensitive detection of the model toxicants; the fluorescent reporter proteins were much more stable, and following long-term exposure allowed detection atlevels similar to that of the bioluminescent sensors. From the two green fluorescent proteins tested, enhanced GFP (EGFP) displayed a more rapid response and higher signal intensity than GFPuv. To combine the advantages of both reporter functions, representatives of both types were jointly encapsulated in a sol-gel matrix and immobilized onto a glass surface, to generate a bioluminescent toxicity and a fluorescent genotoxicity sensor. The dual-function sensor detected both toxic and genotoxic model compounds with no interference from the co-immobilized member.
机译:经过工程改造以响应预定的环境条件而产生可量化信号的转基因细菌,可以用作全细胞生物传感器中的组合传感/报告元件。我们比较了此类细胞中几种可用的报告基因中的两个:绿色荧光蛋白(GFPs)(Aquorea victoria gfp)和生物发光(Vibrio fischeri luxCDABE)基因,它们与SOS(recA)或热休克(grpE)启动子融合。在这两种情况下,细菌生物发光都可以更快,更灵敏地检测模型毒物。荧光报告蛋白更加稳定,并且在长期暴露后,其检测水平与生物发光传感器的水平相似。从测试的两种绿色荧光蛋白中,增强的GFP(EGFP)比GFPuv显示出更快的响应和更高的信号强度。为了结合两种报告功能的优点,将两种类型的代表物共同封装在溶胶-凝胶基质中,并固定在玻璃表面上,以产生生物发光毒性和荧光遗传毒性传感器。双功能传感器可检测到有毒和遗传毒性的模型化合物,而不会受到固定分子的干扰。

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