Abstract
The objective of this study was to develop a biosensor using the cell wall binding domain (CBD) of bacteriophage-encoded peptidoglycan hydrolases (endolysin) immobilized on a gold screen printed electrode (SPE) and subsequent electrochemical impedance spectroscopy (EIS) for a rapid and specific detection of Listeria cells. The endolysin was amine-coupled to SPEs using EDC/NHS chemistry. The CBD-based electrode was used to capture and detect the Listeria innocua serovar 6b from pure culture and 2% artificially contaminated milk. In our study, the endolysin functionalized SPEs have been characterized using X-ray photoelectron spectroscopy (XPS). The integration of endolysin-based recognition for specific bacteria and EIS can be used for direct and rapid detection of Listeria cells with high specificity against non-Listeria cells with a limit of detection of 1.1 × 104 and 105 CFU mL-1 in pure culture and 2% milk, respectively. © The Royal Society of Chemistry 2012.
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CITATION STYLE
Tolba, M., Ahmed, M. U., Tlili, C., Eichenseher, F., Loessner, M. J., & Zourob, M. (2012). A bacteriophage endolysin-based electrochemical impedance biosensor for the rapid detection of Listeria cells. Analyst, 137(24), 5749–5756. https://doi.org/10.1039/c2an35988j
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