Laboratory of Quality & Safety Risk Assessment for Citrus Products (Chongqing), Ministry of Agriculture, Citrus Research Institute, Southwest University, Chongqing, 400712, PR China; National Citrus Engineering Research Center, Chongqing, 400712, PR China.
Laboratory of Quality & Safety Risk Assessment for Citrus Products (Chongqing), Ministry of Agriculture, Citrus Research Institute, Southwest University, Chongqing, 400712, PR China; National Citrus Engineering Research Center, Chongqing, 400712, PR China.
Talanta. 2022 Jan 15;237:122917. doi: 10.1016/j.talanta.2021.122917. Epub 2021 Sep 30.
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.
监测真菌属交链孢霉,它会引起世界范围内的破坏性褐斑病,并产生高毒性的真菌毒素,这对于保护柑橘和人类健康极为重要。在这项工作中,我们描述了一种用于从柑橘果实样本中检测交链孢霉基因组 DNA 的超灵敏比色法,该方法使用由五组报告探针组成的系统。每个报告探针都是通过一种方便且低成本的冷冻辅助方法在金纳米颗粒 (AuNP) 的表面上偶联识别 DNA 和辣根过氧化物酶 (HRP) 制备的。同时,通过生物素-链霉亲和素反应将捕获 DNA 固定在磁性珠 (MB) 上。然后,捕获 DNA、靶 DNA 和五组基于 AuNP 的报告探针在 MB 上形成稳定的 DNA-七聚体夹心结构,然后 HRP 产生蓝色信号进行后续比色检测。值得注意的是,具有大比表面积的 AuNP 驱动大量 HRP 锚定,从而导致显著的信号放大。此外,还有五组基于 AuNP 的报告探针,进一步放大了检测信号。因此,人工靶 DNA 的检测限低至 15.6 pM。由于无需任何特殊设备即可进行可视化记录检测信号,并且具有较高的灵敏度,因此该方法代表了一种用于交链孢霉遗传检测的合适诊断工具。