| F0F1-ATPase分子马达技术对单核细胞增生李斯特菌检测的研究 |
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| 引用本文： | 张捷,张昕,范爱红,张惠媛,汪琦,顾德周,王佩荣,韩晶,陆琳,陈广全,乐加昌. F0F1-ATPase分子马达技术对单核细胞增生李斯特菌检测的研究[J]. 生物技术进展, 2012, 2(6): 436-440. DOI: 10.3969/j.issn.2095-2341.2012.06.09 |
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| 作者姓名： | 张捷 张昕 范爱红 张惠媛 汪琦 顾德周 王佩荣 韩晶 陆琳 陈广全 乐加昌 |
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| 作者单位： | 1.北京出入境检验检疫局, 北京 100026;2.国家认监委认证认可技术研究所, 北京 100020;3.中国科学院生物物理研究所, 北京 100101 |
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| 基金项目： | 国家质检总局科技计划项目(2008IK161)资助。 |
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| 摘 要： | 利用载色体chromatophore上的F0F1-ATPase分子马达生物传感器,建立了应用在食品检测中快速检测方法。首先从嗜热菌中提取载色体后,标记荧光探针F-DHPE,合成生物素化单增李氏菌prfA探针,在已标记F-DHPE的载色体ATP合酶的ε亚基上连接ε亚基抗体-生物素-链霉亲和素-生物素-prfA探针,将待测单核细胞增生李斯特菌标准菌株和阴性对照分别与此生物传感器结合,通过环境H+量测定ATP产生量,进而对单核细胞增生李斯特菌DNA进行检测。结果表明,chro prfA(连接在载色体chro上的prfA探针)的浓度在0.052 mg/mL,单核细胞增生李斯特菌DNA浓度在40 ng/mL为最适检测条件。通过传统检测方法及PCR检测方法对照,本方法具有良好的检测符合性。
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| 关 键 词： | F0F1-ATPase分子马达 单核细胞增生李斯特菌 prfA探针 快速检测 |
| 收稿时间： | 2012-10-09 |
The Study of a Detecting Technology for Listeria monocytogenes based on F0F1-ATPase Molecular Motor Biosensor |
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| ZHANG Jie,ZHANG Xin,FAN Ai-hong,ZHANG Hui-yuan,WANG Qi,GU De-zhou,WANG Pei-rong,HAN Jing,LU Lin,CHEN Guang-quan,YUE Jia-chang. The Study of a Detecting Technology for Listeria monocytogenes based on F0F1-ATPase Molecular Motor Biosensor[J]. CURRENT BIOTECHNOLOGY, 2012, 2(6): 436-440. DOI: 10.3969/j.issn.2095-2341.2012.06.09 |
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| Authors: | ZHANG Jie ZHANG Xin FAN Ai-hong ZHANG Hui-yuan WANG Qi GU De-zhou WANG Pei-rong HAN Jing LU Lin CHEN Guang-quan YUE Jia-chang |
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| Abstract: | A rapid detecting technology was constructed by using chromatophore on the F0F1-ATPase molecular motor biosensor for Listeria monocytogenes in the food. Specific prfA probe were connected with F0F1-ATPase’s ε subunit by using avidin-biotin system, the test samples and negative sample combined with biosensors, respectively, to compare their ATP synthesis by measuring the amount of H+, Listeria monocytogenes DNA in the samples could be tested. The results showed that optimum conditions for detection was using chro prfA concentration of 0.052 mg/mL and Listeria monocytogenes DNA concentration of 40 ng/mL. By contrasting to conventional detection methods and PCR detection method to test the actual samples, this method has good conformity. |
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| Keywords: | F0F1-ATPase molecular motor Listeria monocytogenes prfA probe rapid detection |
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