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Repositorio de la Universidad de Oviedo. > Producción Bibliográfica de UniOvi: RECOPILA > Artículos >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10651/32534

Title: Multiplex Electrochemical DNA Platform for Femtomolar-level Quantification of Genetically Modified Soybean
Author(s): Manzanares Palenzuela, Carmen Lorena
Santos Álvarez, Noemí de los
Lobo Castañón, María Jesús
López Ruiz, Beatriz
Issue date: 2015
Publisher: Elsevier
Publisher version: http://dx.doi.org/10.1016/j.bios.2015.01.007
Citation: Biosensors and Bioelectronics, 68, p. 259-265 (2015); doi:10.1016/j.bios.2015.01.007
Format extent: p. 259-265
Abstract: Current EU regulations on the mandatory labeling of genetically modified organisms (GMOs) with a minimum content of 0.9% would benefit from the availability of reliable and rapid methods to detect and quantify DNA sequences specific for GMOs. Different genosensors have been developed to this aim, mainly intended for GMO screening. A remaining challenge, however, is the development of genosensing platforms for GMO quantification, which should be expressed as the number of event-specific DNA sequences per taxon-specific sequences. Here we report a simple and sensitive multiplexed electrochemical approach for the quantification of Roundup-Ready Soybean (RRS). Two DNA sequences, taxon (lectin) and event-specific (RR), are targeted via hybridization onto magnetic beads. Both sequences are simultaneously detected by performing the immobilization, hybridization and labeling steps in a single tube and parallel electrochemical readout. Hybridization is performed in a sandwich format using signaling probes labeled with fluorescein isothiocyanate (FITC) or digoxigenin (Dig), followed by dual enzymatic labeling using Fab fragments of anti-Dig and anti-FITC conjugated to peroxidase or alkaline phosphatase, respectively. Electrochemical measurement of the enzyme activity is finally performed on screen-printed carbon electrodes. The assay gave a linear range of 2-250 pM for both targets, with LOD values of 650 fM (160 amol) and 190 fM (50 amol) for the event-specific and the taxon-specific targets, respectively. Results indicate that the method could be applied for GMO quantification below the European labeling threshold level (0.9%), offering a general approach for the rapid quantification of specific GMO events in foods
URI: http://hdl.handle.net/10651/32534
ISSN: 0956-5663
1873-4235
Sponsored: This work has been developed in the frame of the GMOensor project of International Research Staff Exchange Scheme(FP7)PEOPLE-2013-IRSES(Marie Curie actions), and supported by the Ministerio de Educación y Ciencia (Spain) Project CTQ2012-31157,and the European Regional Development Fund
Project id.: info:eu-repo/grantAgreement/EC/FP7/612545
MICINN/CTQ2012-31157
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