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dc.provenanceINTA-
dc.contributorBarrera, Viviana Andrea-
dc.contributorGutierrez, Susana-
dc.contributorCúndom, María A.-
dc.contributorGasoni, Amelia L.-
dc.creatorBarrera, Viviana Andrea-
dc.creatorGutierrez, Susana-
dc.creatorCúndom, María A.-
dc.creatorGasoni, Amelia L.-
dc.date2017-08-18T16:05:53Z-
dc.date2017-08-18T16:05:53Z-
dc.date2015-04-01-
dc.date.accessioned2019-04-29T16:26:29Z-
dc.date.available2019-04-29T16:26:29Z-
dc.date.issued2017-08-18T16:05:53Z-
dc.date.issued2017-08-18T16:05:53Z-
dc.date.issued2015-04-01-
dc.identifier1851-7617-
dc.identifier10.1016/j.ram.2015.02.005-
dc.identifierhttp://hdl.handle.net/20.500.12123/994-
dc.identifierhttp://www.elsevier.es/es-revista-revista-argentina-microbiologia-372-articulo-nuclear-acridine-orange-fluorescence-in-S0325754115000358-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/313295-
dc.descriptionThe genus Rhizoctonia DC (1805) has long been studied as an important soilborne pathogen that causes a wide variety of symptoms because it is a non-specialized pathogen3. Rhizoctonia sensu lato is characterized by the lack of conidiogenous cells and this taxon is composed of two groups based on the number of nuclei per cell: the multinucleate group that belongs to Rhizoctonia s. str. and the binucleate group that belongs to Ceratorhiza5. Currently, other authors consider the group a Ceratobasidium–Rhizoctonia complex7 and divide it into two groups: BNR (binucleate Rhizoctonia-like) and MNR (multinucleate Rhizoctonia-like)9. Many methods are used to observe the number of nuclei in fungal cells, e.g. safranine O, aniline blue, HCl-Giemsa. Some of these methods apply a staining solution involving laborious, time-consuming procedures that require no equipment (Fig. 1). Other methods use fluorophores, which are rapid and precise-
dc.formatapplication/pdf-
dc.languageeng-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.sourceRevista Argentina de Microbiología 47 (2) : 167-169 (abril - junio 2015)-
dc.sourcereponame:INTA Digital (INTA)-
dc.sourceinstname:Instituto Nacional de Tecnología Agropecuaria-
dc.sourceinstacron:INTA-
dc.source.uri1851-7617-
dc.source.uri10.1016/j.ram.2015.02.005-
dc.source.urihttp://hdl.handle.net/20.500.12123/994-
dc.source.urihttp://www.elsevier.es/es-revista-revista-argentina-microbiologia-372-articulo-nuclear-acridine-orange-fluorescence-in-S0325754115000358-
dc.source.urihttp://hdl.handle.net/20.500.12123/994-
dc.source.urihttp://www.elsevier.es/es-revista-revista-argentina-microbiologia-372-articulo-nuclear-acridine-orange-fluorescence-in-S0325754115000358-
dc.subjectRhizoctonia-
dc.subjectArroz-
dc.subjectAcridina-
dc.subjectNúcleo-
dc.subjectRice-
dc.subjectAcridine-
dc.subjectNuclear-
dc.titleNuclear acridine orange fluorescence in Rhizoctonia isolates from rice-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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