| Literature DB >> 31198030 |
Qian Wang1,2, Yanli Wen1, Yan Li1, Wen Liang1, Wen Li1, Yuan Li1, Jiahuan Wu1, Huichen Zhu1, Keke Zhao1, Jun Zhang1, Nengqin Jia2, Wangping Deng3, Gang Liu1.
Abstract
Traditional microbiology analysis is usually hindered by the long time-cost and lack of portability in many urgent situations. In this work, we developed a novel electrochemical DNA biosensor (E-biosensor) for sensitive analysis of the 16S rRNA gene of five bacteria, using a consecutive adenine (polyA) probe. The polyA probe consists of a polyA tail and a recognition part. The polyA tail can combine onto the gold surface with improved controllability of the surface density, by conveniently changing the length of polyA. The recognition part of the capture probe together with two biotin-labeled reporter probes hybridize with the target DNA and form a stable DNA-tetramer sandwich structure, and then avidin-HRP enzyme was added to produce a redox current signal for the following electrochemical detection. Finally, we realized sensitive quantification of artificial target DNA with a limit of detection (LOD) of 10 fM, and excellent selectivity and reusability were also demonstrated. Importantly, the detection capability was equally good when facing bacterial genomic DNA, due to the base-stacking force of our multireporter-probe system, which can help to break the second structure and stabilize the probe-target complexes. Our biosensor was constructed on a 16-channel electrode chip without any polymerase chain reaction (PCR) process needed, which took a significant step toward a portable bacteria biosensor.Entities:
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Year: 2019 PMID: 31198030 DOI: 10.1021/acs.analchem.9b02175
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986