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MPCR方法检测食品中的伤寒沙门氏菌、金黄色葡萄球菌和单增李斯特氏菌

Detection of sallmonella typhi, staphylococcus aureus and listeria monocytogenes by multiplex PCR

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【作者】 何浩吴永生刘思国徐贵生郑超张健

【Author】 HE Hao1, WU Yong-sheng1, LIU Si-guo2, XU Gui-sheng1, ZHENG Chao1, ZHANG Jian1 (1. Suifenhe Entry-Exit Inspection and Quarantine Bureau, Suifenhe 157300; 2. Harbin Veterinary Research Institute, Harbin 150001)

【机构】 绥芬河出入境检检疫局哈尔滨兽医研究所绥芬河出入境检检疫局 绥芬河157300绥芬河157300哈尔滨150001

【摘要】 为建立一种同时检测食品中的伤寒沙门氏菌(ST)、金黄色葡萄球菌(SA)和单增李斯特氏菌(LM)的快速检测方法,分别针对伤寒沙门氏菌的鞭毛抗原基因H1-d、金黄色葡萄球菌的耐热核酸酶基因nuc、单增李斯特氏菌溶血素O上的hlyA基因设计引物,进行特异性和灵敏性实验,结果表明3条特异性扩增片段分别为458bp、279bp和243bp,经DNA测序证明其序列与模板被扩增片段一致。该方法操作简便、快速,具有良好的灵敏性和特异性。

【Abstract】 For establish a rapid method to test sallmonella typhi, staphylococcus aureus and listeria monocytogenes in food, so designed three specific primers according to ST, SA and LM. The target gene was amplified from the three bacterium chromosomal DNA by using PCR technique. Then we detect that if the method was specific and sensitive. Electrophoresis products indicate there are three strips in 458bp, 279bp and 243bp. Extraction the target strips sequence analysis indicate nucleotide sequences are consistent with the templates. Proving the specimen are positive. The products reveal that this method provides a specific, sensitive, swift and simple means for the three bacterium mentioned above.

  • 【文献出处】 食品科技 ,Food Science and Technology , 编辑部邮箱 ,2006年09期
  • 【分类号】TS207.4
  • 【被引频次】6
  • 【下载频次】228
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