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作 者:刘立兵[1,2] 南汇珠 孙晓霞 姜彦芬[1] 王金凤 王建昌 LIU Libing;NAN Huizhu;SUN Xiaoxia;JIANG Yanfen;WANG Jinfeng;WANG Jianchang(Hebei Entry-Exit Inspection and Quarantine Technical Center, Shijiazhuang 050051, China;Hebei Academy of Science and Technology for Inspection and Quarantine, Shijiazhuang 050051, China)
机构地区:[1]河北出入境检验检疫局技术中心,河北石家庄050051 [2]河北省检验检疫科学技术研究院,河北石家庄050051
出 处:《食品科学技术学报》2018年第1期89-94,共6页Journal of Food Science and Technology
基 金:国家质量监督检验检疫总局科研项目(2016IK107)
摘 要:为实现简便快速地检测蜡样芽胞杆菌(Bacillus cereus),根据Gen Bank中蜡样芽胞杆菌16 S RNA序列设计特异性引物和exo探针,建立了一种实时荧光重组酶聚合酶扩增方法,在39℃恒温下仅需20 min即可完成检测。该方法特异性扩增蜡样芽胞杆菌16 S RNA基因片段,对其他芽胞杆菌和非芽胞杆菌无扩增;以蜡样芽胞杆菌基因组DNA作为模板,该方法的检测灵敏度为1.0×10-3ng/μL,同已发表的real-time PCR方法一致。人工污染实验表明,当大米饭中蜡样芽胞杆菌污染量≥1.5×104CFU/g时,即可通过real-time RPA方法检出,所需时间仅为6~13min;而当污染量≥1.5×105CFU/g时,才能通过real-time PCR方法检出,所需时间至少为30 min(Ct值为20~31)。The study established a simple and rapid method for the determination of Bacillus cereus. According to the 16 S RNA gene sequences of Bacillus cereus available in Genbank,specific primers and exo probe were designed for establishing real-time recombinase polymerase amplification( real-time RPA).The RPA reaction was performed successfully at 39 ℃ and the results were obtained within 20 min. This method could specifically detect Bacillus cereus,but could not detect other bacteria. The study showed that the detection limit of real-time RPA was 1. 0 × 10^-3 ng/μL with genomic DNA of Bacillus cereus,which was the same as the real-time PCR method. Bacillus cereus in artificially contaminated rice samples with a bacterial concentration of 1. 5 × 10^4 CFU/g could be detected after 6-13 min by real-time RPA;when the bacterial concentration was 1. 5 × 10^5 CFU/g,the Bacillus cereus could be detected at least 30 min by real-time PCR( the Ct value was between 20 and 31).
关 键 词:蜡样芽胞杆菌 等温扩增 实时荧光RPA 检测方法
分 类 号:TS207.4[轻工技术与工程—食品科学] R155.5[轻工技术与工程—食品科学与工程]
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