Department of Medical Microbiology and Parasitology, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia.
World J Microbiol Biotechnol. 2012 Apr;28(4):1699-706. doi: 10.1007/s11274-011-0978-x. Epub 2011 Dec 18.
A disposable horseradish peroxidase (HRP)-based electrochemical genosensor was developed for chronoamperometric detection of single-stranded asymmetric lolB gene PCR amplicon (118 bp in length) of the food-borne pathogen, Vibrio cholerae. A two-step sandwich-type hybridization strategy using two specific probes was employed for specific detection of the target single-stranded DNA (ssDNA). The analytical performances of the detection platform have been evaluated using a synthetic ssDNA (ST3) which was identical to the target single-stranded amplicon and a total of 19 bacterial strains. Under optimal condition, ST3 was calibrated with a dynamic range of 0.4883-15.6250 nM. By coupling asymmetric PCR amplification, the probe-based electrochemical genosensor was highly specific to the target organism (100% specificity) and able to detect as little as 0.85 ng/μl of V. cholerae genomic DNA.
一种一次性辣根过氧化物酶(HRP)电化学基因传感器被开发出来,用于对食源性致病菌霍乱弧菌的单链非对称 lolB 基因 PCR 扩增子(长度为 118bp)进行计时安培检测。采用两步夹心杂交策略,使用两个特异性探针,特异性检测目标单链 DNA(ssDNA)。使用与目标单链扩增子完全相同的合成 ssDNA(ST3)和总共 19 种细菌菌株评估了检测平台的分析性能。在最佳条件下,ST3 的动态范围为 0.4883-15.6250 nM。通过偶联不对称 PCR 扩增,基于探针的电化学基因传感器对目标生物具有高度特异性(100%特异性),能够检测到低至 0.85ng/μl 的霍乱弧菌基因组 DNA。