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Title: | Detection of the shrimp pathogenic bacteria, Vibrio harveyi, by a quartz crystal microbalance-specific antibody based sensor |
Authors: | Buchatip S. Ananthanawat C. Sithigorngul P. Sangvanich P. Rengpipat S. Hoven V.P. |
Keywords: | Alkanethiols Binding efficiency Bovine serum albumins Carbodiimides Carboxyl groups Cross-reactivity Gold electrodes Hydroxyl-terminated Mixed SAM Monoclonal antibodies (mAb) N-hydroxysuccinimide Pathogenic bacterium Penaeus monodon Shrimp culture Vibrio parahaemolyticus Vibrio vulnificus Working range Bacteriology Body fluids Chemical detection Immunosensors Monoclonal antibodies Oxide minerals Piezoelectric devices Quartz Quartz crystal microbalances Self assembled monolayers Surface plasmon resonance Bacteria |
Issue Date: | 2010 |
Abstract: | An immunosensor based on a quartz crystal microbalance (QCM) was developed for detection of Vibrio harveyi (V. harveyi), a pathogenic bacteria causing morbidity and even a high level of fatality in commercial shrimp cultures, including Penaeus monodon. Immobilization of a monoclonal antibody (MAb) against V. harveyi onto the gold electrode of a QCM plate involved a three-step procedure: (1) the formation of a self-assembled monolayer (SAM) of a carboxyl-terminated alkanethiol, (2) activation of the carboxyl groups by N-hydroxysuccinimide (NHS) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC), and (3) attachment of the MAb to the activated carboxyl groups. The developed QCM-based immunosensor could be used for the detection of V. harveyi in a working range of 103-107 CFU/mL, with no detectable cross-reactivity to Vibrio vulnificus and Vibrio parahaemolyticus. Controlling the density of surface-immobilized MAb, by the formation of mixed SAMs containing hydroxyl-terminated alkanethiol in combination with the treatment of 1% (w/v) bovine serum albumin (BSA) as a blocking reagent, can significantly improve the binding efficiency of the targeted bacteria. © 2009 Elsevier B.V. All rights reserved. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14717 https://www.scopus.com/inward/record.uri?eid=2-s2.0-77149134952&doi=10.1016%2fj.snb.2009.12.003&partnerID=40&md5=551ba7bef5f35c7986374b46df1a3695 |
ISSN: | 9254005 |
Appears in Collections: | Scopus 1983-2021 |
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