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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/67517
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dc.contributor.authorFerreira-Nozawa, Monica S.-
dc.contributor.authorNozawa, Sérgio R.-
dc.contributor.authorMartinez-Rossi, Nilce M.-
dc.contributor.authorRossi, Antonio-
dc.date.accessioned2014-05-27T11:20:57Z-
dc.date.accessioned2016-10-25T18:19:06Z-
dc.date.available2014-05-27T11:20:57Z-
dc.date.available2016-10-25T18:19:06Z-
dc.date.issued2003-12-01-
dc.identifierhttp://dx.doi.org/10.1590/S1517-83822003000200014-
dc.identifier.citationBrazilian Journal of Microbiology, v. 34, n. 2, p. 161-164, 2003.-
dc.identifier.issn1517-8382-
dc.identifier.urihttp://hdl.handle.net/11449/67517-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67517-
dc.description.abstractIn this communication, we show that the growth of isolate H6 of the dermatophyte Trichophyton rubrum on non-buffered medium and under saturating phosphate conditions is dependent on the initial growth pH, with an apparent optimum at pH 4.0. In addition, irrespective of the initial growth pH, the pH of the medium altered during cultivation reaching values that ranged from 8.3 to 8.9. Furthermore, this isolate synthesized and secreted almost the same levels of an alkaline phosphatase with an apparent optimum pH ranging from 9.0 to 10.0 when grown on both low- and high-phosphate medium. Also, this alkaline phosphatase is activated by Mg2+ and is EDTA-sensitive. On the other hand, the very low levels of the enzyme retained by the mycelium grown on buffered medium at pH 5.0-5.2 suggest that this enzyme is encoded by an alkaline gene, i.e., a gene responsive to ambient pH signaling.en
dc.format.extent161-164-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAlkaline phosphatase-
dc.subjectAmbient pH-
dc.subjectDermatophytes-
dc.subjectEnzyme secretion-
dc.subjectPi sensing-
dc.subjectTrichophyton rubrum-
dc.subjectArthrodermataceae-
dc.titleThe dermatophyte Trichophyton rubrum secretes an EDTA-sensitive alkaline phosphatase on high-phosphate mediumen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Genética Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, Ribeirão Preto, SP-
dc.description.affiliationInstituto de Biociências Universidade Estadual Paulista, Rio Claro, SP-
dc.description.affiliationDepartamento de Bioquímica e Imunologia Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, Ribeirão Preto, SP-
dc.description.affiliationDepartamento de Genética FMRP, Av. Bandeirantes 3900, 14049-900, Ribeirão Preto, SP-
dc.description.affiliationUnespInstituto de Biociências Universidade Estadual Paulista, Rio Claro, SP-
dc.identifier.doi10.1590/S1517-83822003000200014-
dc.identifier.scieloS1517-83822003000200014-
dc.identifier.wosWOS:000186438800014-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-19844366606.pdf-
dc.relation.ispartofBrazilian Journal of Microbiology-
dc.identifier.scopus2-s2.0-19844366606-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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