化学
辣根过氧化物酶
DNA
检出限
基因组DNA
杂交探针
链霉亲和素
分子生物学
色谱法
胶体金
生物素
生物化学
纳米颗粒
酶
纳米技术
生物
材料科学
作者
Yue He,Jing Zhou,Ruijie Fu,Yanlin Liu,Yiwen Wang,Haoran Liu,Jing Zhao,Yongliang Cui,Bining Jiao
出处
期刊:Talanta
[Elsevier BV]
日期:2021-09-30
卷期号:237: 122917-122917
被引量:12
标识
DOI:10.1016/j.talanta.2021.122917
摘要
The monitoring of the fungal genus Alternaria, which causes destructive brown spot disease in citruses worldwide and produces highly toxic mycotoxins, is extremely important to protect citrus and human health. In this work, we describe an ultrasensitive colorimetric method for the detection of genomic DNA of Alternaria from citrus fruit samples, using a system consisting of five groups of reporter probes. Each reporter probe is prepared by coupling recognition DNA and horseradish peroxidase (HRP) on the surface of gold nanoparticle (AuNP) through a convenient and low-cost freezing-assisted method. Meanwhile, the capture DNA is immobilized on magnetic bead (MB) via biotin-streptavidin reaction. Then, the capture DNA, target DNA, and five groups of AuNP-based reporter probes form a stable DNA-heptamer sandwich structure on the MB, and then HRP generates a blue signal for the subsequent colorimetric detection. It should be noted that AuNP with a large specific surface area drives abundant HRP anchoring, resulting in significant signal amplification. In addition, there are five groups of AuNP-based reporter probes, which further amplify the detection signal. As a result, the detection limit of the artificial target DNA is as low as 15.6 pM. Because the detection signal can be recorded visually without any special equipment, and its sensitivity is high, this method represents a suitable diagnostic tool for Alternaria genetic detection.
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