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首页> 外文期刊>PLoS One >Quantitative bioluminescence assay for measuring Bacillus cereus nonhemolytic enterotoxin complex
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Quantitative bioluminescence assay for measuring Bacillus cereus nonhemolytic enterotoxin complex

机译:测量芽孢杆菌非肿瘤肠毒素复合物的定量生物发光测定

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摘要

Bacillus cereus is a foodborne pathogen causing emesis and diarrhea in those affected. It is assumed that the non-hemolytic enterotoxin (Nhe) plays a key role in B . cereus induced diarrhea. The ability to trace Nhe activity is important for food safety. While assays such as PCR and ELISA exist to detect Nhe, those methods cannot differentiate between active and inactive forms of Nhe. The existing rabbit ileal loop bioassay used to detect Nhe activity is ethically disfavored because it uses live experimental animals. Here we present a custom built low-cost CCD based luminometer and applied it in conjunction with a cell-based assay using Vero cells transduced to express the luciferase enzyme. The activity of Nhe was measured as its ability to inhibit synthesis of luciferase as quantified by reduction of light emission by the luciferase reaction. Emitted light intensity was observed to be inversely proportional to Nhe concentration over a range of 7 ng/ml to 125 ng/ml, with a limit of detection of 7 ng/ml Nhe.
机译:芽孢杆菌是一种食用病原体,导致受影响的人的呕吐和腹泻。假设非溶血肠毒素(NHE)在B中发挥着关键作用。豆类诱发腹泻。追踪NHE活动的能力对于食品安全是重要的。虽然存在诸如PCR和ELISA的测定以检测NHE,但这些方法不能区分NHE的活性和无活性形式。用于检测NHE活性的现有的兔ILEAL环形生物测定是道德不受欢迎的,因为它使用实时实验动物。在这里,我们介绍了一种自定义内置的基于低成本CCD的发光计,并使用转导的Vero细胞结合基于细胞的测定来表达荧光素酶的测定。测量NHE的活性作为抑制通过荧光素酶反应减少发光的量化的荧光素酶合成的能力。观察到发射的光强度与NHE浓度成反比,在7ng / ml至125ng / ml的范围内,其检测限为7 ng / ml NHE。

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