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作 者:齐炳尧 宋广萍 卜胜君 殷奎德[1] 万家余[2] QI Bingyao;SONG Guangping;BU Shengjun;YIN kuide;WAN Jiayu(College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China;Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun 130122, China)
机构地区:[1]黑龙江八一农垦大学生命科学技术学院,大庆163319 [2]军事医学科学院军事兽医研究所,长春130122
出 处:《吉林农业大学学报》2018年第3期369-374,共6页Journal of Jilin Agricultural University
基 金:吉林省科技发展计划项目(20140101027JC;20150101105JC)
摘 要:为将无酶点击化学连接链式反应(CCLCR)结合试纸条用于金黄色葡萄球菌核酸的可视化检测。根据金黄色葡萄球菌16S rRNA的一段保守序列设计1对特异性核酸分子探针,一条探针5'端修饰生物素(Biotin),3'端修饰叠氮(N3);另一条探针5'端修饰环辛炔(DBCO),3'端修饰异硫氰酸荧光素(FITC),通过与目标基因进行特异性杂交,CCLCR和热循环作用下扩增产物进行试纸条分析。结果表明:CCLCR最佳探针浓度为0.05μmol/L,热循环扩增的最佳连接温度为25℃,该方法能够特异性检测出金黄色葡萄球菌核酸,而对肠炎沙门氏菌等其他5种食源性病原菌的检测结果呈阴性,同时对金黄色葡萄球菌核酸的检测灵敏度为1×10-8μmol/L。综上,将CCLCR与试纸条结合作为检测金黄色葡萄球菌的方法,具有操作简单、检测准确、检测成本低等优点,有望作为金黄色葡萄球菌的常规检测方法。This study aims to develop a method for the visualization of Staphylococcus aureus nucleic acid by combining enzyme-free click chemical ligation chain reaction( CCLCR) with test strips. A pair of specific nucleic acid probes was designed according to a conservative sequence of 16 sr DNA of Staphylococcus aureus. One probe modified biotin at the 5' end and N3 at the 3' end. The other probe modified DBCO and FITC,the product was hybridized with the target gene and the reaction product was detected by the test strip. The optimum temperature for CCLCR probe was 0. 05 μmol/L and the optimal temperature for thermocycling was 25 ℃. This method could specifically detect the nucleic acid of Staphylococcus aureus,and the detection result of other 5 foodborne pathogens such as Salmonella et. was negative,while the detection sensitivity of Staphylococcus aureus nucleic acid was 1×10^-8 μmol/L. In summary,the method of combining CCLCR with test strip for Staphylococcus aureus detection has the advantages of simple operation,accurate detection,low cost,etc.,and is expected to serve as a routine detection of Staphylococcus aureus.
关 键 词:金黄色葡萄球菌 无酶点击化学连接链式反应 试纸条 灵敏性 特异性
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