首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >Rapid detection of Listeria monocytogenes using quantum dots and nanobeads-based optical biosensor.
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Rapid detection of Listeria monocytogenes using quantum dots and nanobeads-based optical biosensor.

机译:使用量子点和基于纳米珠的光学生物传感器快速检测李斯特菌。

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摘要

A rapid, specific method was developed to detect Listeria monocytogenes using magnetic nanobeads to separate and concentrate the target bacteria and quantum dots (QDs) as fluorescent markers. QDs are semiconductor nanocrystals which measure from a few nanometers to a few hundred nanometers, and are particularly significant in optical detections due to their high quantum yield. Both streptavidin conjugated QDs 605 and magnetic nanobeads were separately coated with specific biotin-conjugated anti-L. monocytogenes antibody. The conjugated magnetic nanobeads were then mixed with L. monocytogenes culture dilutions. After immunomagnetic separation, the magnetic nanobeads-L. monocytogenes conjugates were mixed with conjugated QDs. Unattached conjugated QDs were removed using immunomagnetic separation. A fluorescence spectrometer was used to measure the fluorescence of the complexes of magnetic beads-L. monocytogene-QDs. Results indicated that this method could detect L. monocytogenes at a concentration of 2-3 cfu/mL in a pure culture. A linear co-relationship was found between the fluorescence intensity and L. monocytogenes in a range of 100-107 cfu/mL. The total detection time was 1.5 h..
机译:开发了一种快速,特异性的方法来检测单核细胞增生李斯特菌,方法是使用磁性纳米珠分离并浓缩靶细菌和量子点(QD)作为荧光标记。 QD是尺寸从几纳米到几百纳米的半导体纳米晶体,由于其高量子产率而在光学检测中尤为重要。链霉亲和素缀合的QD 605和磁性纳米珠都分别涂有特异性生物素缀合的抗L。单核细胞增生因子抗体。然后将缀合的磁性纳米珠与单核细胞增生李斯特氏菌培养物稀释液混合。免疫磁分离后,磁性纳米珠-L。将单核细胞增生因子结合物与结合的QD混合。使用免疫磁分离法去除未连接的共轭QD。使用荧光光谱仪测量磁珠-L的复合物的荧光。单核细胞增生症结果表明,该方法可以在纯培养物中检测2-3 cfu / mL浓度的单核细胞增生李斯特菌。发现荧光强度和单核细胞增生李斯特氏菌之间的线性关系为100-107 cfu / mL。总检测时间为1.5小时。

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