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Establishment of multiplex PCR for screening Escherichia coli and Salmonella in Chinese herbal medicine

机译:中草药中大肠杆菌和沙门氏菌多重PCR筛选方法的建立

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The purpose is to study a multiplex PCR method for screening qualified Chinese herbal medicine granules for pharmaceutical enterprises. In this experiment, the uidA gene in Escherichia coli genome, inv A gene in Salmonella genome and 16S rDNA were used as target genes. Three pairs of primers were selected to establish and optimize the multiplex PCR system for the detection of bacteria in drugs. The amplified products were 194 bp, 362 bp and 1374 bp, respectively. The specificity of the multiplex PCR was verified by 11 strains of bacteria. The results showed that the sensitivity of multiplex PCR detection could reach $10^{3}-10^{4}$ CFU/ml at the cell level; bacteria were found in two of the six drugs tested in the market; bacteria were found in all the four drugs that did not pass the drug test, but none of the tested drugs had Escherichia coli and Salmonella. The results showed that the multiplex PCR detection method could detect Escherichia coli and Salmonella in Chinese herbal medicine granules rapidly, accurately and efficiently, which provided reference for the preliminary screening of Chinese herbal medicine granules.
机译:研究一种用于制药企业筛选合格中药颗粒的多重PCR方法。本实验以大肠杆菌基因组中的uidA基因、沙门氏菌基因组中的inv A基因和16S rDNA为靶基因。选择三对引物,建立并优化了检测药物中细菌的多重PCR系统。扩增产物分别为194bp、362bp和1374bp。多重PCR的特异性得到了11株细菌的验证。结果表明,在细胞水平上,多重PCR检测的灵敏度可达$10^{3}-10^{4}$CFU/ml;在市场上测试的六种药物中,有两种发现了细菌;在所有四种未通过药物测试的药物中都发现了细菌,但测试药物中没有一种含有大肠杆菌和沙门氏菌。结果表明,多重PCR检测方法能快速、准确、高效地检测中草药颗粒中的大肠杆菌和沙门氏菌,为中草药颗粒的初步筛选提供了参考。

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