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基于扩增阻滞突变系统聚合酶链反应(ARMS-PCR)的泰国可食用燕窝基因鉴定

Genetic Identification of Edible Bird's Nest in Thailand Based on ARMS-PCR.

作者信息

Lv Dongyong, Fan Yaohua, Zhong Wanhua, Lonan Piyanuch, Liu Kunfeng, Wu Maoyong, Wu Yina, Liang Yueliang, Lai Xiaoping, Li Geng, Yu Liangwen

机构信息

School of Nursing, Guangzhou University of Chinese Medicine, Guangzhou, China.

Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine, Guangzhou University of Chinese Medicine, Shenzhen, China.

出版信息

Front Genet. 2021 Mar 8;12:632232. doi: 10.3389/fgene.2021.632232. eCollection 2021.

Abstract

Edible bird's nest (EBN) is a popular delicacy in the Asian Pacific region originating from Indonesia, Malaysia, Thailand and Vietnam, which consist of various potential medicine value in Traditional Chinese Medicine (TCM). Thailand is one of the main exporters of EBN. However, the genetic information of EBN, a key part of molecular biology, has yet to be reported in Thailand. It is necessary to explore the genetic information of EBN in Thailand based on a quick and simple method to help protect the rights and interests of consumers. This research aimed to systematically evaluate different methods of extracting EBN DNA to improve the efficiency of the analysis of cytochrome b (Cytb) and NADH dehydrogenase subunit 2 (ND2) gene sequences, the establishment of phylogenetic trees, and the genetic information of EBN in Thailand. Additionally, we aimed to develop a quick and simple method for identifying EBN from different species based on the genetic information and amplification-refractory mutation system PCR (ARMS-PCR). By comparing the four methods [cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS), kit and guanidinium isothiocyanate methods] for EBN extraction, we found that the guanidinium isothiocyanate method was the optimal extraction method. Phylogenetic trees generated on the basis of Cytb and ND2 gene analyses showed that 26 samples of house EBN and 4 samples of cave EBN came from and , respectively. In addition, to distinguish different samples from different species of , we designed 4 polymerase chain reaction (PCR) amplification primers based on the ND2 gene sequences of and . The ARMS-PCR results showed band lengths for EBN of 533, 402, and 201 bp, while those for EBN were 463, 317, and 201 bp. Collectively, the results showed that ARMS-PCR is a fast and simple method for the genetic identification of EBN based on designing specific original identification primers.

摘要

燕窝是亚太地区颇受欢迎的美食,原产于印度尼西亚、马来西亚、泰国和越南,在传统中医中具有多种潜在药用价值。泰国是燕窝的主要出口国之一。然而,燕窝的遗传信息作为分子生物学的关键部分,在泰国尚未见报道。有必要基于快速简便的方法探索泰国燕窝的遗传信息,以保护消费者权益。本研究旨在系统评估不同的燕窝DNA提取方法,以提高细胞色素b(Cytb)和烟酰胺腺嘌呤二核苷酸脱氢酶亚基2(ND2)基因序列分析、系统发育树构建以及泰国燕窝遗传信息分析的效率。此外,我们旨在基于遗传信息和扩增阻滞突变系统PCR(ARMS-PCR)开发一种快速简便的方法,用于从不同物种中鉴定燕窝。通过比较四种燕窝提取方法[十六烷基三甲基溴化铵(CTAB)法、十二烷基硫酸钠(SDS)法、试剂盒法和异硫氰酸胍法],我们发现异硫氰酸胍法是最佳提取方法。基于Cytb和ND2基因分析生成的系统发育树表明,26个家燕燕窝样本和4个洞燕燕窝样本分别来自[具体来源未给出]和[具体来源未给出]。此外,为了区分不同物种的不同样本,我们基于[具体物种未给出]和[具体物种未给出]的ND2基因序列设计了4对聚合酶链反应(PCR)扩增引物。ARMS-PCR结果显示,[具体物种未给出]燕窝的条带长度为533、402和201 bp,而[具体物种未给出]燕窝的条带长度为463、317和201 bp。总体而言,结果表明ARMS-PCR是一种基于设计特异性原始鉴定引物对燕窝进行遗传鉴定的快速简便方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3004/7983251/f54dcc0f6eac/fgene-12-632232-g001.jpg

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