Electrochemical genosensor for specific detection of the food-borne pathogen, Vibrio cholerae
Identifieur interne : 002560 ( Main/Exploration ); précédent : 002559; suivant : 002561Electrochemical genosensor for specific detection of the food-borne pathogen, Vibrio cholerae
Auteurs : Kim-Fatt Low [Malaisie] ; Kritsanaporn Chuenrangsikul [Thaïlande] ; Patsamon Rijiravanich [Thaïlande] ; Werasak Surareungchai [Thaïlande] ; Yean-Yean Chan [Malaisie]Source :
- World Journal of Microbiology and Biotechnology [ 0959-3993 ] ; 2012-04-01.
English descriptors
- KwdEn :
Abstract
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.
Url:
DOI: 10.1007/s11274-011-0978-x
Affiliations:
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<front><div type="abstract" xml:lang="en">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.</div>
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