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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69594
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dc.contributor.authorXimenes, Valdecir Farias-
dc.contributor.authorFernandes, João Roberto-
dc.contributor.authorBueno, Vânia B.-
dc.contributor.authorCatalani, Luiz H.-
dc.contributor.authorOliveira, Georgino H. de-
dc.contributor.authorMachado, Rosângela G. P.-
dc.date.accessioned2014-05-27T11:22:26Z-
dc.date.accessioned2016-10-25T18:23:43Z-
dc.date.available2014-05-27T11:22:26Z-
dc.date.available2016-10-25T18:23:43Z-
dc.date.issued2007-04-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1600-079X.2007.00419.x-
dc.identifier.citationJournal of Pineal Research, v. 42, n. 3, p. 291-296, 2007.-
dc.identifier.issn0742-3098-
dc.identifier.issn1600-079X-
dc.identifier.urihttp://hdl.handle.net/11449/69594-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69594-
dc.description.abstractThere is a growing body of evidence that melatonin and its oxidation product, N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK), have anti-inflammatory properties. From a nutritional point of view, the discovery of melatonin in plant tissues emphasizes the importance of its relationship with plant peroxidases. Here we found that the pH of the reaction mixture has a profound influence in the reaction rate and products distribution when melatonin is oxidized by the plant enzyme horseradish peroxidase. At pH 5.5, 1 mm of melatonin was almost completely oxidized within 2 min, whereas only about 3% was consumed at pH 7.4. However, the relative yield of AFMK was higher in physiological pH. Radical-mediated oxidation products, including 2-hydroxymelatonin, a dimer of 2-hydroxymelatonin and O-demethylated dimer of melatonin account for the fast consumption of melatonin at pH 5.5. The higher production of AFMK at pH 7.4 was explained by the involvement of compound III of peroxidases as evidenced by spectral studies. On the other hand, the fast oxidative degradation at pH 5.5 was explained by the classic peroxidase cycle. © 2007 The Authors.en
dc.format.extent291-296-
dc.language.isoeng-
dc.sourceScopus-
dc.subject2-hydroxymelatonin-
dc.subjectHorseradish peroxidase-
dc.subjectMelatonin-
dc.subjectMelatonin dimer-
dc.subjectN 1-acetyl-N2-formyl-5-methoxykynuramine-
dc.subjecthorseradish peroxidase-
dc.subjectmelatonin-
dc.subjectmelatonin derivative-
dc.subjectn1 acetyl n2 formyl 5 methoxykynuramine-
dc.subjectunclassified drug-
dc.subjectcatalysis-
dc.subjectcatalyst-
dc.subjectchemical reaction-
dc.subjectdemethylation-
dc.subjectenzyme activity-
dc.subjectenzyme metabolism-
dc.subjectmethylation-
dc.subjectnonhuman-
dc.subjectoxidation-
dc.subjectpH-
dc.subjectHorseradish Peroxidase-
dc.subjectHydrogen-Ion Concentration-
dc.subjectKynuramine-
dc.subjectOxidation-Reduction-
dc.titleThe effect of pH on horseradish peroxidase-catalyzed oxidation of melatonin: Production of N1-acetyl-N2-formyl-5- methoxykynuramine versus radical-mediated degradationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationDepartamento de Química Faculdade de Ciências Universidade Estadual Paulista, Bauru-
dc.description.affiliationInstituto de Química Universidade de São Paulo, São Paulo-
dc.description.affiliationDepartamento de Princípios Ativos e Naturais Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, Araraquara, São Paulo-
dc.description.affiliationDepartamento de Química Faculdade de Ciências de Bauru Universidade Do Estado de São Paulo, CEP 17033-360-
dc.description.affiliationUnespDepartamento de Química Faculdade de Ciências Universidade Estadual Paulista, Bauru-
dc.description.affiliationUnespDepartamento de Princípios Ativos e Naturais Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, Araraquara, São Paulo-
dc.identifier.doi10.1111/j.1600-079X.2007.00419.x-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Pineal Research-
dc.identifier.scopus2-s2.0-33847641335-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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