| Literature DB >> 28213234 |
Dilsat Ozkan-Ariksoysal1, Yasin Ugur Kayran2, Fethiye Ferda Yilmaz3, Anton Alexandru Ciucu4, Iulia Gabriela David4, Vasile David4, Mine Hosgor-Limoncu3, Mehmet Ozsoz2.
Abstract
This paper introduces DNA-wrapped multi-walled carbon nanotube (MWCNT)-modified genosensor for the detection of Escherichia coli (E. coli) from polymerase chain reaction (PCR)-amplified real samples while Staphylococcus aureus (S. aureus) was used to investigate the selectivity of the biosensor. The capture probe specifically recognizing E. coli DNA and it was firstly interacted with MWCNTs for wrapping of single-stranded DNA (ssDNA) onto the nanomaterial. DNA-wrapped MWCNTs were then immobilised on the surface of disposable pencil graphite electrode (PGE) for the detection of DNA hybridization. Electrochemical behaviors of the modified PGEs were investigated using Raman spectroscopy and differential pulse voltammetry (DPV). The sequence selective DNA hybridization was determined and evaluated by changes in the intrinsic guanine oxidation signal at about 1.0V by DPV. Numerous factors affecting the hybridization were optimized such as target concentration, hybridization time, etc. The designed DNA sensor can well detect E. coli DNA in 20min detection time with 0.5pmole of detection limit in 30µL of sample volume. Copyright ÂEntities:
Keywords: DNA Hybridization; DNA-wrapped multi-walled carbon nanotubes; Electrochemical DNA biosensor; Escherichia coli detection; Pencil graphite electrode (PGE); Polymerase chain reaction (PCR) amplified real samples
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Year: 2017 PMID: 28213234 DOI: 10.1016/j.talanta.2017.01.005
Source DB: PubMed Journal: Talanta ISSN: 0039-9140 Impact factor: 6.057