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PCR 法检测食品中大肠杆菌O157:H7
引用本文:巢强国,杨学明,葛宇,熊薇,曲勤凤,王瑞元. PCR 法检测食品中大肠杆菌O157:H7[J]. 食品科学, 2010, 31(8): 212-215. DOI: 10.7506/spkx1002-6300-201008047
作者姓名:巢强国  杨学明  葛宇  熊薇  曲勤凤  王瑞元
作者单位:1.上海市质量监督检验技术研究院 2.华东理工大学生物工程学院
基金项目:上海市质量监督检验局项目(2007-21)
摘    要:对大肠杆菌O157:H7 型菌株的各毒力基因及基因组中的特异序列进行了设计和比对,确定292bp 的检测引物。常规定性PCR 和实时定量PCR 证明该引物特异性强。模拟样品的前增菌实验结果表明本方法可以在原样品活菌浓度约2.0CFU/mL 时通过16h 增菌后检测出来,总的检测时间可以控制在24h 内。本实验建立的PCR 方法可用于食品中大肠杆菌O157:H7 的快速测定。

关 键 词:大肠杆菌O157:H7  食源性致病菌  特异序列  PCR  
收稿时间:2009-03-03

Rapid PCR Detection of Enterohemorrhagic Escherichia coli O157:H7 in Foods
CHAO Qiang-guo,YANG Xue-ming,GE Yu,XIONG Wei,QU Qin-feng,WANG Rui-yuan. Rapid PCR Detection of Enterohemorrhagic Escherichia coli O157:H7 in Foods[J]. Food Science, 2010, 31(8): 212-215. DOI: 10.7506/spkx1002-6300-201008047
Authors:CHAO Qiang-guo  YANG Xue-ming  GE Yu  XIONG Wei  QU Qin-feng  WANG Rui-yuan
Affiliation:1. Shanghai Institute of Quality Inspection and Technical Research, Shanghai 200233, China;2. School of Bioengineering, East China University of Science and Technology, Shanghai 200237, China
Abstract:Genomic comparisons were carried out on Escherichia coli virulence genes and genome-specific sequences,which were located in the genomes of Escherichia coli serotype O157:H7 strains released in the GenBank.One pair of primers specific for ECs3032 genes was exploited for the amplification to give a 292 bp PCR product.Conventional qualitative PCR and real-time quantitative PCR assays showed higher specificity of the primers.The assays were used for detecting Escherichia coli O157:H7 in ground beef initially i...
Keywords:enterohemorrhagic Escherichia coli O157:H7  foodborne pathogenic bacteria  specific sequence  PCR  
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