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利用寡核苷酸功能化金纳米颗粒在压电生物传感器上快速检测食源性病原体。

Using oligonucleotide-functionalized Au nanoparticles to rapidly detect foodborne pathogens on a piezoelectric biosensor.

作者信息

Chen Sz-Hau, Wu Vivian C H, Chuang Yao-Chen, Lin Chih-Sheng

机构信息

Department of Biological Science and Technology, National Chiao Tung University, Hsinchu 30005, Taiwan.

出版信息

J Microbiol Methods. 2008 Apr;73(1):7-17. doi: 10.1016/j.mimet.2008.01.004. Epub 2008 Jan 18.

Abstract

A circulating-flow piezoelectric biosensor, based on an Au nanoparticle amplification and verification method, was used for real-time detection of a foodborne pathogen, Escherichia coli O157:H7. A synthesized thiolated probe (Probe 1; 30-mer) specific to E. coli O157:H7 eaeA gene was immobilized onto the piezoelectric biosensor surface. Hybridization was induced by exposing the immobilized probe to the E. coli O157:H7 eaeA gene fragment (104-bp) amplified by PCR, resulting in a mass change and a consequent frequency shift of the piezoelectric biosensor. A second thiolated probe (Probe 2), complementary to the target sequence, was conjugated to the Au nanoparticles and used as a "mass enhancer" and "sequence verifier" to amplify the frequency change of the piezoelectric biosensor. The PCR products amplified from concentrations of 1.2 x 10(2) CFU/ml of E. coli O157:H7 were detectable by the piezoelectric biosensor. A linear correlation was found when the E. coli O157:H7 detected from 10(2) to 10(6) CFU/ml. The piezoelectric biosensor was able to detect targets from real food samples.

摘要

一种基于金纳米颗粒扩增和验证方法的循环流动压电生物传感器,用于实时检测食源性病原体大肠杆菌O157:H7。将合成的针对大肠杆菌O157:H7 eaeA基因的硫醇化探针(探针1;30聚体)固定在压电生物传感器表面。通过将固定的探针暴露于经聚合酶链反应(PCR)扩增的大肠杆菌O157:H7 eaeA基因片段(104碱基对)来诱导杂交,导致压电生物传感器发生质量变化并随之产生频率偏移。与靶序列互补的第二个硫醇化探针(探针2)与金纳米颗粒结合,并用作“质量增强剂”和“序列验证剂”以放大压电生物传感器的频率变化。从浓度为1.2×10²CFU/ml的大肠杆菌O157:H7扩增得到的PCR产物可被压电生物传感器检测到。当检测到的大肠杆菌O157:H7浓度在10²至10⁶CFU/ml之间时,发现存在线性相关性。该压电生物传感器能够检测实际食品样品中的靶标。

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