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dc.contributor.author | Santiago Felipe, Sara | es_ES |
dc.contributor.author | Tortajada-Genaro, Luis Antonio | es_ES |
dc.contributor.author | Morais, Sergi | es_ES |
dc.contributor.author | Puchades, Rosa | es_ES |
dc.contributor.author | Maquieira Catala, Ángel | es_ES |
dc.date.accessioned | 2016-06-17T10:40:47Z | |
dc.date.available | 2016-06-17T10:40:47Z | |
dc.date.issued | 2015-05-01 | |
dc.identifier.issn | 0308-8146 | |
dc.identifier.uri | http://hdl.handle.net/10251/66087 | |
dc.description.abstract | [EN] A valid solution for micro-analytical systems is the selection of a compatible amplification reaction with a simple, highly-integrated efficient design that allows the detection of multiple genomic targets. Two approaches under isothermal conditions are presented: recombinase polymerase amplification (RPA) and multiple displacement amplification (MDA). Both methods were applied to a duplex assay specific for Salmonella spp. and Cronobacter spp., with excellent amplification yields (0.2 8.6 108 fold). The proposed approaches were successfully compared to conventional PCR and tested for the milk sample analysis as a microarray format on a compact disc (support and driver). Satisfactory results were obtained in terms of resistance to inhibition, selectivity, sensitivity (101 102 CFU/mL) and reproducibility (below 12.5%). The methods studied are efficient and cost-effective, with a high potential to automate microorganisms detection by integrated analytical systems working at a constant low temperature. | es_ES |
dc.description.sponsorship | Funding projects MINECO CTQ2013-45875-R and GV PrometeoII/2014/040. MECD provided S.S.F with a PhD grant. | en_EN |
dc.language | Inglés | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation.ispartof | Food Chemistry | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Isothermal DNA amplification | es_ES |
dc.subject | Pathogens | es_ES |
dc.subject | Milk | es_ES |
dc.subject | Microarraying | es_ES |
dc.subject.classification | QUIMICA ANALITICA | es_ES |
dc.title | Isothermal DNA amplification strategies for duplex microorganism detection | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1016/j.foodchem.2014.11.080 | |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//CTQ2013-45875-R/ES/BIOSENSADO EN SOPORTES INTERACTIVOS CON PROPIEDADES INTERFEROMETRICAS PARA APLICACIONES CLINICAS. DEMOSTRACION EN FARMACOGENETICA Y ALERGIAS MEDICAMENTOSAS/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//PROMETEOII%2F2014%2F040/ES/Estudio de estrategias fisico-químicas para el desarrollo de biosensores interferométricos en soportes interactivos de aplicación en clínica/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Química - Departament de Química | es_ES |
dc.description.bibliographicCitation | Santiago Felipe, S.; Tortajada-Genaro, LA.; Morais, S.; Puchades, R.; Maquieira Catala, Á. (2015). Isothermal DNA amplification strategies for duplex microorganism detection. Food Chemistry. 174:509-515. https://doi.org/10.1016/j.foodchem.2014.11.080 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://dx.doi.org/10.1016/j.foodchem.2014.11.080 | es_ES |
dc.description.upvformatpinicio | 509 | es_ES |
dc.description.upvformatpfin | 515 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 174 | es_ES |
dc.relation.senia | 277149 | es_ES |
dc.identifier.eissn | 1873-7072 | |
dc.identifier.pmid | 25529713 | |
dc.contributor.funder | Ministerio de Economía y Competitividad | |
dc.contributor.funder | Generalitat Valenciana |