We report a nuclease-responsive DNA probe platform integrated with magnetic separation for ultrarapid and sensitive bacterial detection. The sensing strategy employs dual-labeled DNA probes featuring a 3'-biotin and a 5'-signal reporter (fluorophore, enzyme, or chromophore), which undergo cleavage by nucleases released from viable bacteria. Streptavidin-conjugated magnetic nanoparticles enable efficient separation of cleaved signal fragments from biotin bound strands, thereby minimizing background noise and maximizing assay specificity. The entire workflow-including bacterial lysis, enzymatic cleavage, magnetic separation, and signal readout-can be completed within 3 min. Using Escherichia coli as a model, the platform achieved detection limits below 10 CFU per reaction with fluorescence or chemiluminescence methods, and as few as 102 CFU per reaction with a colorimetric method. This platform selectively detected viable bacteria and demonstrates real-world applicability through a custom-designed point-of-care testing (POCT) device, which successfully identified simulated bacterial contamination in various food samples. Overall, this technology offers a practical and rapid solution for frontline microbial surveillance in food and environmental safety.
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Sun-Jung Kim
Da Jung Chung
김수민
ACS Applied Bio Materials
Korea Research Institute of Bioscience and Biotechnology
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Kim et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69a75c19c6e9836116a248fd — DOI: https://doi.org/10.1021/acsabm.5c02030
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