Generation and use of site-directed chromosomal cyaA’ translational fusions in Salmonella enterica.

dc.contributor.authorRamos Morales, Francisco
dc.contributor.authorCardenal Muñoz, Elena
dc.contributor.authorCordero Alba, Mar
dc.contributor.authorBaisón Olmo, Fernando
dc.date.accessioned2025-02-03T07:32:57Z
dc.date.available2025-02-03T07:32:57Z
dc.date.issued2015
dc.departamentoBiología Celular, Genética y Fisiología
dc.descriptionhttps://www.springernature.com/gp/open-science/policies/book-policieses_ES
dc.description.abstractCyaA from Bordetella pertussis is a calmodulin-dependent adenylate cyclase. Fusions to the catalytic domain of CyaA (CyaA’) are useful tools to detect translocation of type III secretion system effectors from Gram-negative pathogens like Salmonella enterica. These fusions are usually generated using plasmids with strong promoters. Here, we describe a protocol to insert the CyaA’-encoding sequence in a specific site in the bacterial chromosome in order to get a monocopy fusion whose expression is driven by the native promoter. We also describe the procedure to detect translocation of a CyaA’ fusion into mammalian cells.es_ES
dc.identifier.citationRamos-Morales F, Cardenal-Muñoz E, Cordero-Alba M, Baisón-Olmo F. Generation and use of site-directed chromosomal cyaA' translational fusions in Salmonella enterica. Methods Mol Biol. 2015;1225:93-104. doi: 10.1007/978-1-4939-1625-2_6. PMID: 25253250.es_ES
dc.identifier.doi10.1007/978-1-4939-1625-2_6
dc.identifier.urihttps://hdl.handle.net/10630/37565
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectTranslocación (Genética)es_ES
dc.subjectSalmonella - Genéticaes_ES
dc.subjectBacterias gram negativases_ES
dc.subjectBacterias - Metabolismoes_ES
dc.subject.otherEffectorses_ES
dc.subject.otherTranslocationes_ES
dc.subject.otherCyaAes_ES
dc.subject.othercAMPes_ES
dc.subject.otherSalmonellaes_ES
dc.subject.otherChromosomal translational fusionses_ES
dc.subject.otherType III secretiones_ES
dc.titleGeneration and use of site-directed chromosomal cyaA’ translational fusions in Salmonella enterica.es_ES
dc.typebook partes_ES
dc.type.hasVersionSMURes_ES
dspace.entity.typePublication

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