Rapid and visual detection of Listeria monocytogenes based on nanoparticle cluster catalyzed signal amplification.
Rapid and visual detection of Listeria monocytogenes based on nanoparticle cluster catalyzed signal amplification.
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DOI:
10.1016/j.bios.2016.05.100
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发表时间:
2016-12
影响因子:
12.6
通讯作者:
Lisha Zhang;R. Huang;Weipeng Liu;Hongxing Liu;Xiaoming Zhou;D. Xing
中科院分区:
文献类型:
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作者:
Lisha Zhang;R. Huang;Weipeng Liu;Hongxing Liu;Xiaoming Zhou;D. Xing
Foodborne pathogens pose a significant threat to human health worldwide. The identification of foodborne pathogens needs to be rapid, accurate and convenient. Here, we constructed a nanoparticle cluster (NPC) catalyzed signal amplification biosensor for foodborne pathogens visual detection. In this work, vancomycin (Van), a glycopeptide antibiotic for Gram-positive bacteria, was used as the first molecular recognition agent to captureListeriamonocytogenes(L. monocytogenes). Fe3O4NPC modified aptamer, was used as the signal amplification nanoprobe, specifically recognize to the cell wall ofL. monocytogenes. As vancomycin and aptamer recognizeL. monocytogenesat different sites, the sandwich recognition showed satisfied specificity. Compared to individual Fe3O4nanoparticle (NP), NPC exhibit collective effect-enhanced catalytic activity for the color reaction of chromogenic substrate. The change in absorbance or color could represent the concentration of target. Using the Fe3O4NPC-based signal amplification method,L. monocytogeneswhole cells could be directly assayed within a linear range of 5.4×103–108cfu/mL and a visual limit of detection of 5.4×103cfu/mL. Fe3O4NPC-based method was more sensitive than the Fe3O4NP-based method. All these attractive characteristics of highly sensitivity, visual and labor-saving, make the biosensor possess a potential application for foodborne pathogenic bacteria detection.