金黄色葡萄球菌
重组酶聚合酶扩增
清脆的
量油尺
病毒学
生物
聚合酶链反应
细菌
遗传学
基因
尿
生物化学
作者
Li‐Yun Lin,Guangcai Zha,Huagui Wei,Yuzhong Zheng,Peikui Yang,Yaqun Liu,Mouquan Liu,Zhonghe Wang,Xianghui Zou,Hui Zhu,Qiulan Luo,Jinquan Li,Min Lin
出处
期刊:Food Control
[Elsevier]
日期:2022-11-10
卷期号:145: 109505-109505
被引量:19
标识
DOI:10.1016/j.foodcont.2022.109505
摘要
At present, the main challenge for Staphylococcus aureus (S. aureus) in food safety is still a lack of rapid, convenient detection methods. This study developed a combination of recombinase polymerase amplification (RPA) and the CRISPR-Cas12a technology (known as the RPA-CRISPR-Cas12a assay) for the detection of S. aureus in food. This novel assay could detect samples with a fluorescence reader, lateral flow dipstick (LFD) or the naked eye under a UV transilluminator. After optimization, the RPA-CRISPR-Cas12a assay could specifically and stably detect S. aureus as low as 1–10 copies/μL within 40 min at 37 °C. This assay had high sensitivity to the detection of S. aureus in both laboratory standard samples and field samples, which indicated the feasibility of this assay. To sum up, this accurate, portable detection method for S. aureus has great potential applications in food safety, especially in the field, without requiring sophisticated equipment or high level of technical expertise.
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