Kim Cheol Min, Jang Cheol Seong
Plant Genomics Laboratory, Interdisciplinary Program in Smart Agriculture, Kangwon National University, Chuncheon, 24341 Republic of Korea.
Food Sci Biotechnol. 2025 Apr 4;34(11):2553-2562. doi: 10.1007/s10068-025-01874-3. eCollection 2025 Jul.
The consumption of wild plants, raw or cooked, is a common practice across many countries. However, some wild plants have toxins harmful to humans. In this study, we developed specific primer targeting chloroplast genes to distinguish the edible plant, , and the toxic plant, The performance of the designed primers was evaluated through a qPCR assay, assessing their specificity, sensitivity, and practical applicability. Six primer (three each for and ) demonstrated linearity with correlation coefficients above 0.99 and slopes ranging from - 3.337 to - 3.581. PCR efficiencies were calculated to range from 90.28 to 97.86%, with a detection limit of 0.001 ng of DNA, and a quantitative threshold of 0.1% (w/w). The specificity was confirmed with 13 non-target plant species, and efficiency validated using 15 commercial samples. The assay help prevent mistaking toxic wild plants and provide guidelines to identify toxic plants for public safety.
The online version contains supplementary material available at 10.1007/s10068-025-01874-3.
食用生的或煮熟的野生植物在许多国家都是常见的做法。然而,一些野生植物含有对人类有害的毒素。在本研究中,我们开发了针对叶绿体基因的特异性引物,以区分可食用植物和有毒植物。通过定量聚合酶链反应(qPCR)分析评估所设计引物的性能,评估其特异性、灵敏度和实际适用性。六种引物(每种植物各三种)表现出线性关系,相关系数高于0.99,斜率范围为-3.337至-3.581。计算出的聚合酶链反应效率范围为90.28%至97.86%,检测限为0.001纳克DNA,定量阈值为0.1%(重量/重量)。用13种非目标植物物种确认了特异性,并使用15个商业样品验证了效率。该分析有助于防止误食有毒野生植物,并为识别有毒植物以保障公共安全提供指导。
在线版本包含可在10.1007/s10068-025-01874-3获取的补充材料。