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野味物种鉴定:重组酶聚合酶扩增(RPA)结合侧向流动(LF)试纸条用于鉴定台湾梅花鹿()。

Bushmeat Species Identification: Recombinase Polymerase Amplification (RPA) Combined with Lateral Flow (LF) Strip for Identification of Formosan Reeves' Muntjac ().

作者信息

Hsu Yun-Hsiu, Yang Wei-Cheng, Chan Kun-Wei

机构信息

Department of Veterinary Medicine, College of Veterinary Medicine, National Chiayi University, Chiayi 60054, Taiwan.

Department of Veterinary Medicine, School of Veterinary Medicine, National Taiwan University, Taipei 10617, Taiwan.

出版信息

Animals (Basel). 2021 Feb 7;11(2):426. doi: 10.3390/ani11020426.

Abstract

The identification of animal species of meat in meat products is of great concern for various reasons, such as public health, religious beliefs, food allergies, legal perspectives, and bushmeat control. In this study, we developed a new technique to identify Formosan Reeves' muntjac in meat using recombinase polymerase amplification (RPA) in combination with a lateral flow (LF) strip. The DNA extracted from a piece of Formosan Reeves' muntjac meat was amplified by a pair of specific primers based on its mitochondrial cytochrome b gene for 10 min at a constant temperature ranging from 30 to 45 °C using RPA. Using the specific probe added to the RPA reaction system, the amplified products were visualized on the LF strip within 5 min. The total operating time from quick DNA extraction to visualizing the result was approximately 30 min. The RPA-LF system we designed was efficient when using boiled, pan-fried, roasted, stir-fried, or stewed samples. The advantages of simple operation, speediness, and cost-effectiveness make our RPA-LF method a promising molecular detection tool for meat species identification of either raw or variously cooked Formosan Reeves' muntjac meat. It is also possible to apply this method to identify the meat of other wildlife sources.

摘要

出于多种原因,如公共卫生、宗教信仰、食物过敏、法律层面以及野味管控等,肉制品中肉类动物物种的鉴定备受关注。在本研究中,我们开发了一种新技术,利用重组酶聚合酶扩增(RPA)结合侧向流(LF)试纸条来鉴定肉中的台湾梅花鹿。从一块台湾梅花鹿肉中提取的DNA,使用RPA,基于其线粒体细胞色素b基因,通过一对特异性引物在30至45°C的恒温下扩增10分钟。在RPA反应体系中加入特异性探针后,扩增产物在5分钟内在LF试纸上可视化。从快速DNA提取到结果可视化的总操作时间约为30分钟。我们设计的RPA-LF系统在使用水煮、煎、烤、炒或炖的样品时效率很高。操作简单、快速且具有成本效益的优点,使我们的RPA-LF方法成为一种有前景的分子检测工具,可用于鉴定生的或经过各种烹饪的台湾梅花鹿肉的肉类物种。将该方法应用于鉴定其他野生动物来源的肉也是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b90/7914887/412603d88bd5/animals-11-00426-g001.jpg

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