首页> 外文期刊>Journal of food protection >Detection of Escherichia coli O157, Salmonella enterica Serovar Typhimurium, and Staphylococcal Enterotoxin B in a Single Sample Using Enzymatic Bio-Nanotransduction
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Detection of Escherichia coli O157, Salmonella enterica Serovar Typhimurium, and Staphylococcal Enterotoxin B in a Single Sample Using Enzymatic Bio-Nanotransduction

机译:使用酶促生物纳米转导检测单个样品中的大肠杆菌O157,肠炎沙门氏菌血清型鼠伤寒杆菌和葡萄球菌肠毒素B

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Enzymatic bio-nanotransduction is a biological detection scheme based on the production of nucleic acid nano-signals (RNA) in response to specific biological recognition events. In this study, we applied an enzymatic bio-nanotransduction system to the detection of important food-related pathogens and a toxin. Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and staphylococcal enterotoxin B (SEB) were chosen because of the implications of these targets to food safety. Primary antibodies to each of the targets were used to functionalize magnetic beads and produce biological recognition elements (antibodies) conjugated to nano-signal-producing DNA templates. Immunomagnetic capture that was followed by in vitro transcription of DNA templates bound to target molecules produced RNA nano-signals specific for every target in the sample. Discrimination of RNA nano-signals with a standard enzyme-linked oligonucleotide fluorescence assay provided a correlation between nano-signal profiles and target concentrations. The estimated limit of detection was 2.4 x 10~3 CFU/ml for E. coli O157:H7, 1.9 x 10~4 CFU/ml for S. enterica serovar Typhimurium, and 0.11 ng/ml for SEB with multianalyte detection in buffer. Low levels of one target were also detected in the presence of interference from high levels of the other targets. Finally, targets were detected in milk, and detection was improved for E. coli O157 by heat treatment of the milk.
机译:酶促生物纳米转导是一种生物检测方案,基于对特定生物识别事件的响应而产生的核酸纳米信号(RNA)。在这项研究中,我们将酶促生物纳米转导系统应用于重要的食物相关病原体和毒素的检测。选择大肠杆菌O157:H7,肠沙门氏菌血清鼠伤寒沙门氏菌和葡萄球菌肠毒素B(SEB),因为这些目标对食品安全性有影响。针对每个靶标的一抗用于功能化磁珠,并产生与识别纳米信号的DNA模板偶联的生物识别元件(抗体)。免疫磁捕获,然后体外转录与靶分子结合的DNA模板,产生了对样品中每个靶特异的RNA纳米信号。用标准的酶联寡核苷酸荧光分析法对RNA纳米信号的区分提供了纳米信号曲线与目标浓度之间的相关性。估计的检出限为:大肠杆菌O157:H7为2.4 x 10〜3 CFU / ml,肠炎链球菌血清鼠伤寒为1.9 x 10〜4 CFU / ml,SEB为0.11 ng / ml,在缓冲液中进行多分析物检测。在其他目标物的高水平干扰下,也检测到一个目标物的低水平。最后,在牛奶中检测到目标,并通过热处理牛奶来改善大肠杆菌O157的检测。

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