Ultrasensitive detection of aflatoxin B1 by SERS aptasensor based on exonuclease-assisted recycling amplification

核酸外切酶 III 检出限 核酸外切酶 黄曲霉毒素 适体 化学 DNA 色谱法 表面增强拉曼光谱 琼脂糖 线性范围 胶体金 拉曼散射 纳米颗粒 材料科学 拉曼光谱 纳米技术 聚合酶 生物化学 分子生物学 大肠杆菌 生物 食品科学 基因 物理 光学
作者
Qin Li,Zhicheng Lü,Xuecai Tan,Xiaoyan Xiao,Pan Wang,Long Biao Wu,Kang Shao,Wenmin Yin,Heyou Han
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:97: 59-64 被引量:156
标识
DOI:10.1016/j.bios.2017.05.031
摘要

Aflatoxin B1 (AFB1) is one of the most abundant and carcinogenic food-contaminating mycotoxins around the world. In this study, we proposed a surface enhanced Raman scattering (SERS) sensing strategy for the determination of AFB1. An aptamer for AFB1 partially hybridized with complementary-DNA, which was released after the recognition of AFB1 and immediately hybridized with hairpin DNA on the surface of sputtering Au film. Exonuclease III hydrolyzed the double-stranded DNA, leaving short single-stranded DNA on the Au surface and releasing complementary-DNA for next ring opening and digestion. SERS tag was captured on Au surface by DNA hybridization. Agarose gel electrophoresis and dynamic light scattering showed that SERS tag was successfully prepared. The detection principle was validated by electrochemical impedance spectroscopy and SERS at each step. High sensitivity and good selectivity for AFB1 detection were observed. The results showed that there was a good linear relation when the AFB1 concentration was from 1×10−6 to 1 ng/mL, and the limit of detection (LOD) was 0.4 fg/mL. This sensor was also applied for quantifying AFB1 levels in spiked peanuts samples, the recoveries was in the range of 89–121%.
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