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Updated: Jun 17, 2026

Development of a Quantitative Recombinase Polymerase Amplification Assay with an Internal Positive Control
Published on: March 30, 2015
Quantification of viable bacteria in fermented foods using an enzymatic cascade-based pre-amplification-free RNA
Xinlei Zhang1, Chunmiao Xu1, Xuhan Xia1
1College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, China. luoam@scu.edu.cn.
None:
Rapid measurement of viable bacteria during fermentation and within fermented food products is important to ensure their quality and safety, however, tools are still lacking. Herein, we developed an LbuCas13a-LbCas12a cascade assay that enables rapid quantification of viable bacteria in fermented foods. By leveraging the cascade reaction to amplify the signal triggered by bacterial RNAs, the assay allows to detect as low as 5 × 103 CFU mL-1 lactic acid bacteria without nucleic acid pre-amplification. Using the assay, we achieved accurate quantification of viable bacteria proportions in heterogeneous populations and successfully evaluated the viable content in fermented dairy products. This strategy provides an efficient molecular tool for quality assessment of fermented food products.
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