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使用1-kb四氢大麻酚酸合酶荧光原位杂交探针鉴定大麻。

Identification of Cannabis sativa L. using the 1-kbTHCA synthase-fluorescence in situ hybridization probe.

作者信息

Jeangkhwoa Pattraporn, Bandhaya Achirapa, Umpunjun Puangpaka, Chuenboonngarm Ngarmnij, Panvisavas Nathinee

机构信息

M.Sc. Program in Plant Science, Department of Plant Science, Faculty of Science and Department of Pharmaceutical Botany, Faculty of Pharmacy, Mahidol University, Thailand.

Forensic Science Program, Faculty of Science, Mahidol University, Thailand.

出版信息

Sci Justice. 2017 Mar;57(2):101-106. doi: 10.1016/j.scijus.2016.11.002. Epub 2016 Nov 5.

Abstract

This study reports a successful application of fluorescence in situ hybridization (FISH) technique in the identification of Cannabis sativa L. cells recovered from fresh and dried powdered plant materials. Two biotin-16-dUTP-labeled FISH probes were designed from the Cannabis-specific tetrahydrocannabinolic acid synthase (THCAS) gene and the ITS region of the 45S rRNA gene. Specificity of probe-target hybridization was tested against the target and 4 non-target plant species, i.e., Humulus lupulus, Mitragyna speciosa, Papaver sp., and Nicotiana tabacum. The 1-kb THCA synthase hybridization probe gave Cannabis-specific hybridization signals, unlike the 700-bp Cannabis-ITS hybridization probe. Probe-target hybridization was also confirmed against 20 individual Cannabis plant samples. The 1-kb THCA synthase and 700-bp Cannabis-ITS hybridization probes clearly showed 2 hybridization signals per cell with reproducibility. The 1-kb THCA synthase probe did not give any FISH signal when tested against H. lupulus, its closely related member of the Canabaceae family. It was also showed that 1-kb THCA synthase FISH probe can be applied to identify small amount of dried powdered Cannabis material with an addition of rehydration step prior to the experimental process. This study provided an alternative identification method for Cannabis trace.

摘要

本研究报告了荧光原位杂交(FISH)技术在从新鲜和干燥的植物粉末材料中回收的大麻细胞鉴定中的成功应用。从大麻特异性四氢大麻酚酸合酶(THCAS)基因和45S rRNA基因的ITS区域设计了两种生物素-16-dUTP标记的FISH探针。针对目标植物和4种非目标植物物种,即啤酒花、帽柱木、罂粟和烟草,测试了探针-靶标杂交的特异性。与700bp的大麻ITS杂交探针不同,1kb的THCA合酶杂交探针给出了大麻特异性杂交信号。还针对20个单独的大麻植物样本证实了探针-靶标杂交。1kb的THCA合酶和700bp的大麻ITS杂交探针在每个细胞中清晰地显示出2个具有可重复性的杂交信号。当针对大麻科的近缘成员啤酒花进行测试时,1kb的THCA合酶探针未给出任何FISH信号。研究还表明,在实验过程之前增加复水步骤,1kb的THCA合酶FISH探针可用于鉴定少量干燥的大麻粉末材料。本研究为大麻痕量鉴定提供了一种替代方法。

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