Electrochemical genosensor for specific detection of the food-borne pathogen, Vibrio cholerae

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Author listLow K.-F., Chuenrangsikul K., Rijiravanich P., Surareungchai W., Chan Y.-Y.

PublisherSpringer

Publication year2012

JournalWorld Journal of Microbiology and Biotechnology (0959-3993)

Volume number28

Issue number4

Start page1699

End page1706

Number of pages8

ISSN0959-3993

eISSN1573-0972

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84859266304&doi=10.1007%2fs11274-011-0978-x&partnerID=40&md5=4b5728e71dda591fe11660e182d32164

LanguagesEnglish-Great Britain (EN-GB)


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Abstract

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. © 2011 Springer Science+Business Media B.V.


Keywords

Asymmetric PCR ampliconCarbon screen-printed electrodeChronoamperometryProbe-based sandwich-type hybridizationVibrio cholerae


Last updated on 2023-01-10 at 07:35