Suppr超能文献

利用定量实时聚合酶链反应开发区分可食用植物和有毒植物的分子标记。

Development of molecular markers for distinguishing between the edible plant and the toxic plant using quantitative real-time polymerase chain reaction.

作者信息

Kim Cheol Min, Jang Cheol Seong

机构信息

Plant Genomics Laboratory, Interdisciplinary Program in Smart Agriculture, Kangwon National University, Chuncheon, 24341 Republic of Korea.

出版信息

Food Sci Biotechnol. 2025 Apr 4;34(11):2553-2562. doi: 10.1007/s10068-025-01874-3. eCollection 2025 Jul.

Abstract

UNLABELLED

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.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s10068-025-01874-3.

摘要

未标注

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。

补充信息

在线版本包含可在10.1007/s10068-025-01874-3获取的补充材料。

相似文献

1
Development of molecular markers for distinguishing between the edible plant and the toxic plant using quantitative real-time polymerase chain reaction.
Food Sci Biotechnol. 2025 Apr 4;34(11):2553-2562. doi: 10.1007/s10068-025-01874-3. eCollection 2025 Jul.
2
Laboratory-based molecular test alternatives to RT-PCR for the diagnosis of SARS-CoV-2 infection.
Cochrane Database Syst Rev. 2024 Oct 14;10(10):CD015618. doi: 10.1002/14651858.CD015618.
3
Antibody tests for identification of current and past infection with SARS-CoV-2.
Cochrane Database Syst Rev. 2022 Nov 17;11(11):CD013652. doi: 10.1002/14651858.CD013652.pub2.
4
Development of a SYBR Green Real-Time PCR method for the detection of and using chloroplast genes.
Food Sci Biotechnol. 2024 Jun 25;34(1):115-124. doi: 10.1007/s10068-024-01636-7. eCollection 2025 Jan.
5
Rapid, point-of-care antigen tests for diagnosis of SARS-CoV-2 infection.
Cochrane Database Syst Rev. 2022 Jul 22;7(7):CD013705. doi: 10.1002/14651858.CD013705.pub3.
6
Signs and symptoms to determine if a patient presenting in primary care or hospital outpatient settings has COVID-19.
Cochrane Database Syst Rev. 2022 May 20;5(5):CD013665. doi: 10.1002/14651858.CD013665.pub3.
7
Diagnostic test accuracy and cost-effectiveness of tests for codeletion of chromosomal arms 1p and 19q in people with glioma.
Cochrane Database Syst Rev. 2022 Mar 2;3(3):CD013387. doi: 10.1002/14651858.CD013387.pub2.
9
Are Current Survival Prediction Tools Useful When Treating Subsequent Skeletal-related Events From Bone Metastases?
Clin Orthop Relat Res. 2024 Sep 1;482(9):1710-1721. doi: 10.1097/CORR.0000000000003030. Epub 2024 Mar 22.
10
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.

本文引用的文献

1
Development of a SYBR Green Real-Time PCR method for the detection of and using chloroplast genes.
Food Sci Biotechnol. 2024 Jun 25;34(1):115-124. doi: 10.1007/s10068-024-01636-7. eCollection 2025 Jan.
2
Ethnobotanical review of traditional use of wild food plants in Japan.
J Ethnobiol Ethnomed. 2024 Nov 21;20(1):100. doi: 10.1186/s13002-024-00736-2.
3
Development of molecular markers based on real-time PCR to detect flax and sesame in commercial amaranth products.
Food Sci Biotechnol. 2024 May 13;33(14):3313-3322. doi: 10.1007/s10068-024-01584-2. eCollection 2024 Nov.
4
Development of real-time PCR-based markers for differentiation of and in commercial food products.
Food Sci Biotechnol. 2023 Jun 6;32(14):2153-2161. doi: 10.1007/s10068-023-01313-1. eCollection 2023 Dec.
5
Detection of Highly Poisonous Using Quantitative Real-Time PCR with Specific Primers.
Toxins (Basel). 2022 Nov 10;14(11):776. doi: 10.3390/toxins14110776.
6
Petasin is the main component responsible for the anti-adipogenic effect of Petasites japonicus.
Fitoterapia. 2022 Mar;157:105130. doi: 10.1016/j.fitote.2022.105130. Epub 2022 Jan 18.
7
Characterization of the complete chloroplast genome of (Asteraceae).
Mitochondrial DNA B Resour. 2021 Mar 1;6(2):678-679. doi: 10.1080/23802359.2021.1881928.
8
Antioxidant compounds of and their preventive effects in chronic diseases: a review.
J Clin Biochem Nutr. 2020 Jul;67(1):10-18. doi: 10.3164/jcbn.20-58. Epub 2020 Jun 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验