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Detection of Staphylococcus Aureus using quantum dots as fluorescence labels

机译:使用量子点作为荧光标记物检测金黄色葡萄球菌

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Staphylococcus aureus (S. aureus) has been identified as one of the major foodborne pathogenic bacteria. The development of rapid detection methods for S. aureus is needed for assuring food safety. In this study, quantum dots were used as fluorescent labels in an immunoassay for quantitative detection of S. aureus. Firstly, biotin-labeled anti-S. aureus antibody was conjugated with streptavidin-coated magnetic nanobeads (180 nm diameter) and used to separate S. aureus cells. Then streptavidin coated quantum dots (QDs) were conjugated with biotin-labeled anti-S. aureus antibody and used as the fluorescence labels to mix with the separated S. aureus. Finally the fluorescence intensity of the bead-cell-QD complexes was measured at a wavelength of 620 nm. A linear relationship between S. aureus cell number (X) and fluorescence intensity (Y) was found for cell numbers ranging from 103 to 106 CFU (Colony Forming Unit)/mL, and the detection limit was 103 CFU/mL. The regression model can be expressed as Y = 7.68X + 35.06 with R2 =0.94. The detection of S. aureus in food sample was explored initially. The fluorescence intensity of food sample was close to the background, so it was not satisfied. Further study will focus on the application of the method for detection of S. aureus in food sample.
机译:金黄色葡萄球菌(S. aureus)已被确定为主要的食源性致病细菌之一。为了确保食品安全,需要开发金黄色葡萄球菌的快速检测方法。在这项研究中,量子点在免疫测定中用作荧光标记,用于定量检测金黄色葡萄球菌。首先,生物素标记的抗-S。将金黄色葡萄球菌抗体与链霉亲和素包被的磁性纳米珠(直径180 nm)偶联,并用于分离金黄色葡萄球菌细胞。然后将抗生蛋白链菌素包被的量子点(QD)与生物素标记的抗S偶联。金黄色葡萄球菌抗体,用作与分离的金黄色葡萄球菌混合的荧光标记。最后,在620nm的波长下测量了珠细胞-QD复合物的荧光强度。对于103-106 CFU(菌落形成单位)/ mL的细胞数,发现金黄色葡萄球菌细胞数(X)和荧光强度(Y)之间存在线性关系,检出限为103 CFU / mL。回归模型可以表示为Y = 7.68X + 35.06,R2 = 0.94。最初探讨了食品样品中金黄色葡萄球菌的检测。食品样品的荧光强度接近背景,因此不满意。进一步的研究将集中在食品样品中金黄色葡萄球菌检测方法的应用上。

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