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高亲和力截短适体通过磁分离辅助 DNA 酶驱动的 3D DNA walker 检测克罗诺杆菌属。

High-affinity truncated aptamers for detection of Cronobacter spp with magnetic separation-assisted DNAzyme-driven 3D DNA walker.

机构信息

State Key Laboratory of Food Science and Resources, School of Food Science and Technology, International Joint Laboratory On Food Safety, Jiangnan University, Wuxi, 214122, China.

College of Ocean Food and Biological Engineering, Jimmie University, Jimei University, Jimei District, Xiamen City, 361021, Fujian Province, China.

出版信息

Mikrochim Acta. 2024 Feb 13;191(3):130. doi: 10.1007/s00604-024-06199-2.

Abstract

After optimizing the original aptamer sequence by truncation strategy, a magnetic separation-assisted DNAzyme-driven 3D DNA walker fluorescent aptasensor was developed for detecting the food-borne pathogen Cronobacter species. Iron oxide magnetic nanoparticles (MNPs) modified with a hybrid of truncated aptamer probe and DNAzyme strand (AP-E1) denoted as MNPs@AP-E1, were employed as capture probes. Simultaneously, a DNAzyme-driven 3D-DNA walker was utilized as the signal amplification element. The substrate strand (Sub) was conjugated with the gold nanoparticles (AuNPs), resulting in the formation of AuNPs@Sub, which served as a 3D walking track. In the presence of the target bacteria and Mg, E1-DNAzyme was activated and moved along AuNPs@Sub, continuously releasing the signal probe. Under optimized conditions, a strong linear correlation was observed for Cronobacter sakazakii (C. sakazakii) in the concentration range 10 to 10 CFU mL, with a low detection limit of 2 CFU mL. The fluorescence signal responses for different Cronobacter species exhibited insignificant differences, with a relative standard deviation of 3.6%. Moreover, the aptasensor was successfully applied to determine  C. sakazakii in real samples with recoveries of 92.86%-108.33%. Therefore, the novel method could be a good candidate for ultra-sensitive and selective detection of Cronobacter species without complex manipulation.

摘要

通过截短策略对原始适体序列进行优化后,开发了一种基于磁分离辅助 DNA 酶驱动的 3D DNA walker 荧光适体传感器,用于检测食源性致病菌克罗诺杆菌属。用截短的适体探针和 DNA 酶链的混合物修饰的氧化铁磁性纳米粒子(MNPs)(表示为 MNPs@AP-E1)被用作捕获探针。同时,使用 DNA 酶驱动的 3D-DNA walker 作为信号放大元件。底物链(Sub)与金纳米粒子(AuNPs)偶联,形成 AuNPs@Sub,作为 3D 行走轨道。在目标细菌和 Mg 的存在下,E1-DNA 酶被激活并沿着 AuNPs@Sub 移动,不断释放信号探针。在优化条件下,Cronobacter sakazakii(C. sakazakii)在 10 到 10 CFU mL 的浓度范围内呈现出强烈的线性相关性,检测限低至 2 CFU mL。对不同克罗诺杆菌属的荧光信号响应没有显著差异,相对标准偏差为 3.6%。此外,该适体传感器成功地应用于实际样品中 C. sakazakii 的测定,回收率为 92.86%-108.33%。因此,该新方法无需复杂操作即可作为超灵敏和选择性检测克罗诺杆菌属的良好候选方法。

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