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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Application of yeast cells transformed with GFP expression constructs containing the RAD54 or RNR2 promoter as a test for the genotoxic potential of chemical substances.
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Application of yeast cells transformed with GFP expression constructs containing the RAD54 or RNR2 promoter as a test for the genotoxic potential of chemical substances.

机译:应用含有RAD54或RNR2启动子的GFP表达构建体转化的酵母细胞作为化学物质遗传毒性潜力的测试。

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摘要

Yeast strains transformed with high copy number plasmids carrying the gene encoding a green fluorescent protein optimised for yeast (yEGFP3) under the control of the RAD54 or RNR2 promoter were used to investigate the activity of potentially DNA-damaging substances. The assays were performed on 96-well microtitre plates in the presence of different concentrations of the test substances. The synthesis of GFP protein was measured through the fluorescence signal and cell growth was monitored by absorption. Here, we demonstrate that this system can be used as a biosensor to assess the genotoxic potential of drugs and other chemical substances. The use of microtitre plates will enable full automation of the system and allows the inclusion of internal reference standards in each assay.
机译:在RAD54或RNR2启动子的控制下,用高拷贝数质粒转化的酵母菌株携带编码针对酵母优化的绿色荧光蛋白(yEGFP3)的基因,以研究其潜在的破坏DNA物质的活性。在存在不同浓度的测试物质的情况下,在96孔微量滴定板上进行测定。通过荧光信号测量GFP蛋白的合成,并通过吸收监测细胞生长。在这里,我们证明了该系统可以用作生物传感器来评估药物和其他化学物质的遗传毒性潜力。微量滴定板的使用将使系统完全自动化,并允许在每个测定中包括内部参考标准品。

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