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一种基于纳米颗粒扩增的石英晶体微天平DNA传感器,用于检测大肠杆菌O157:H7。

A nanoparticle amplification based quartz crystal microbalance DNA sensor for detection of Escherichia coli O157:H7.

作者信息

Mao Xiaole, Yang Liju, Su Xiao-Li, Li Yanbin

机构信息

Department of Biological and Agricultural Engineering, University of Arkansas, Fayetteville, AR 72701, USA.

出版信息

Biosens Bioelectron. 2006 Jan 15;21(7):1178-85. doi: 10.1016/j.bios.2005.04.021. Epub 2005 Jun 13.

Abstract

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 Fe(3)O(4) 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 O157:H7 cells can be detected by the sensor. Linear correlation between frequency change and logarithmic number of bacterial cell concentration was found for E. coli O157:H7 from 2.67 x 10(2) to 2.67 x 10(6)CFU/ml.

摘要

基于纳米颗粒扩增方法,开发了一种用于检测大肠杆菌O157:H7的石英晶体微天平(QCM)DNA传感器。通过自组装将对大肠杆菌O157:H7 eaeA基因特异的硫醇化单链DNA(ssDNA)探针固定在QCM传感器表面。通过将ssDNA探针暴露于互补靶DNA来诱导杂交,这导致了质量变化,进而引起QCM的频率变化。结合链霉亲和素的Fe(3)O(4)纳米颗粒(平均直径 = 145 nm)用作“质量增强剂”来放大频率变化。测试了合成的生物素化寡核苷酸以及使用生物素标记引物通过不对称PCR扩增的大肠杆菌O157:H7 eaeA基因片段(151个碱基)。该传感器能够检测低至10(-12)M的合成寡核苷酸和2.67 x 10(2)菌落形成单位(CFU)/ml的大肠杆菌O157:H7细胞。对于浓度在2.67 x 10(2)至2.67 x 10(6)CFU/ml之间的大肠杆菌O157:H7,发现频率变化与细菌细胞浓度的对数之间存在线性相关性。

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