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
琼脂糖凝胶电泳
琼脂糖
线性范围
胶体金
分析化学(期刊)
纳米颗粒
材料科学
纳米技术
聚合酶
生物化学
分子生物学
大肠杆菌
生物
基因
食品科学
作者
Qin Li,Zhicheng Lü,Xuecai Tan,Xiaoyan Xiao,Pan Wang,Long Wu,Kang Shao,Wenmin Yin,Heyou Han
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%.
科研通智能强力驱动
Strongly Powered by AbleSci AI