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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A nanoparticle amplification based quartz crystal microbalance DNA sensor for detection of Escherichia coli O157 : H7
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A nanoparticle amplification based quartz crystal microbalance DNA sensor for detection of Escherichia coli O157 : H7

机译:基于纳米粒子扩增的石英晶体微量天平DNA传感器,用于检测大肠杆菌O157:H7

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摘要

A quartz crystal microbalance (QCM) DNA sensor, based on the nanoparticle amplification method, was developed for detection of Escherichia coli O157:H7. A thiolated single-stranded DNA (ssDNA) probe specific to E. coli O157:H7 eaeA gene was immobilized onto the QCM sensor surface through self-assembly. The hybridization was induced by exposing the ssDNA probe to the complementary target DNA, and resulted in the mass change and therefore frequency change of the QCM. Streptavidin conjugated Fe3O4 nanoparticles (average diameter = 145 nm) were used as "mass enhancers" to amplify the frequency change. Synthesized biotinylated oligonucleotides as well as E. coli O157:H7 eaeA gene fragments (151 bases) amplified using asymmetric PCR with biotin labeled primers were tested. As low as 10-12 M synthesized oligonucleotides and 2.67 x 10(2) Colony forming unit (CFU)/ml E. coli 0157:H7 cells can be detected by the sensor. Linear correlation. between frequency change andlogarithmic numberof bacterial cell concentration was found for E. coliO157:H7 from 2.67 x 10(2) to 2.67 x 10(6) CFU/ml. (c) 2005 Elsevier B.V. All rights reserved.
机译:开发了一种基于纳米粒子扩增方法的石英微天平(QCM)DNA传感器,用于检测大肠杆菌O157:H7。通过自组装将特异于大肠杆菌O157:H7 eaeA基因的硫醇化单链DNA(ssDNA)探针固定在QCM传感器表面上。通过将ssDNA探针暴露于互补靶DNA诱导杂交,并导致QCM的质量变化和频率变化。链霉亲和素共轭的Fe3O4纳米颗粒(平均直径= 145 nm)被用作“质量增强剂”来放大频率变化。测试了使用生物素标记引物的不对称PCR扩增的合成生物素化寡核苷酸以及大肠杆菌O157:H7 eaeA基因片段(151个碱基)。传感器可检测低至10-12 M的合成寡核苷酸和2.67 x 10(2)菌落形成单位(CFU)/ ml大肠杆菌0157:H7细胞。线性相关。大肠杆菌O157:H7的频率变化与细菌细胞浓度的对数之间的差从2.67 x 10(2)到2.67 x 10(6)CFU / ml。 (c)2005 Elsevier B.V.保留所有权利。

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