Senior Research Fellow (DRDO-SRF), Defence Food Research Laboratory (DFRL), Mysore 570011, India.
Senior Research Fellow, (Inspire fellow, DST), Defence Food Research Laboratory (DFRL), Mysore 570011, India.
J Microbiol Methods. 2022 Feb;193:106414. doi: 10.1016/j.mimet.2022.106414. Epub 2022 Jan 10.
Aflatoxin B1 contamination in food and agro commodities has been major concern of global food safety and trade industry. There is an urgent need to develop sensitive and on-site detection methods for aflatoxins mainly, AFB1 monitoring. In the present study, a fluorophore (Alexa Fluor 488) based aptamer biosensor was devised in combination with graphene oxide (GO) for the detection of Aflatoxin B1 (AFB1). The optimized diagnostic procedure consisted of a fluorescent modified aptamer (Ax-AFLA5) as detection probe and GO mediated quenching of the same; to the quenched system AFB1 was added resulting in subsequent release of fluorescence. The principle of GO based adsorption of ssDNA and successive desorption in the presence of target mycotoxin was utilised in development of the bioassay. In presence of target mycotoxin, the GO adsorbed ssDNA attained a structural conformation resulting in desorption and subsequent release of fluorescence. Assay parameters such as concentration of fluorescent probe, GO and incubation time were evaluated and optimized. The optical signal thus generated could determine presence of AFB1 in the given sample. Selectivity of the method with other mycotoxins was evaluated. The linear range of AFB1 from 0.2-200 ppb was assessed. Visible green fluorescence release was observed at 20 ppb under UV transilluminator and the detection limit of the developed assay was interpreted as 20 ppb of AFB1. The suitability of the assay for AFB1 quantification in groundnut and natural samples was also evaluated. Thus, the developed assay can be a field deployable, reliable and rapid alternative tool for onsite screening method of aflatoxins and other mycotoxins at field level.
食品和农产品中黄曲霉毒素 B1 的污染一直是全球食品安全和贸易行业的主要关注点。迫切需要开发用于检测黄曲霉毒素的敏感和现场检测方法,主要是 AFB1 监测。在本研究中,设计了一种基于荧光团(Alexa Fluor 488)的适体生物传感器,与氧化石墨烯(GO)结合用于检测黄曲霉毒素 B1(AFB1)。优化后的诊断程序包括作为检测探针的荧光修饰适体(Ax-AFLA5)和 GO 介导的相同物的猝灭;向猝灭系统中加入 AFB1 导致随后释放荧光。在存在目标真菌毒素的情况下,利用 GO 对 ssDNA 的吸附及其在存在目标真菌毒素的情况下的解吸原理来开发生物测定法。在存在目标真菌毒素的情况下,GO 吸附的 ssDNA 获得结构构象,导致解吸和随后释放荧光。评估和优化了荧光探针、GO 和孵育时间的浓度等分析参数。由此产生的光学信号可确定给定样品中是否存在 AFB1。评估了该方法对其他真菌毒素的选择性。评估了 AFB1 从 0.2-200 ppb 的线性范围。在紫外透射光下观察到 20 ppb 时可见绿色荧光释放,并且所开发的测定法的检测限解释为 20 ppb 的 AFB1。还评估了该测定法在花生和天然样品中用于 AFB1 定量的适用性。因此,所开发的测定法可作为现场部署的、可靠的和快速的替代工具,用于现场筛选黄曲霉毒素和其他真菌毒素的现场筛选方法。