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Campo DC | Valor | Idioma |
---|---|---|
dc.contributor.author | Ximenes, Valdecir Farias | - |
dc.contributor.author | Fernandes, João Roberto | - |
dc.contributor.author | Bueno, Vania B. | - |
dc.contributor.author | Catalani, Luiz H. | - |
dc.contributor.author | de Oliveira, Georgino H. | - |
dc.contributor.author | Machado, Rosangela G. P. | - |
dc.date.accessioned | 2014-05-20T13:24:26Z | - |
dc.date.accessioned | 2016-10-25T16:45:08Z | - |
dc.date.available | 2014-05-20T13:24:26Z | - |
dc.date.available | 2016-10-25T16:45:08Z | - |
dc.date.issued | 2007-04-01 | - |
dc.identifier | http://dx.doi.org/10.1111/j.1600-076X.2007.00419.x | - |
dc.identifier.citation | Journal of Pineal Research. Oxford: Blackwell Publishing, v. 42, n. 3, p. 291-296, 2007. | - |
dc.identifier.issn | 0742-3098 | - |
dc.identifier.uri | http://hdl.handle.net/11449/7570 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/7570 | - |
dc.description.abstract | There is a g-rowing body of evidence that melatonin and its oxidation product, N-1-acetyl-N-2-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. | en |
dc.format.extent | 291-296 | - |
dc.language.iso | eng | - |
dc.publisher | Blackwell Publishing | - |
dc.source | Web of Science | - |
dc.subject | 2-hydroxymelatonin | pt |
dc.subject | horseradish peroxidase | pt |
dc.subject | melatonin | pt |
dc.subject | melatonin dimer | pt |
dc.subject | N-1-acetyl-N-2-formyl-5-methoxykynuramine | pt |
dc.title | The effect of pH on horseradish peroxidase-catalyzed oxidation of melatonin: production of N-1-acetyl-N-2-formyl-5-methoxykynuramine versus radical-mediated degradation | en |
dc.type | outro | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.description.affiliation | Univ Estadual Paulista, Dept Quim, Fac Ciências, Bauru, Brazil | - |
dc.description.affiliation | Univ São Paulo, Inst Quim, São Paulo, Brazil | - |
dc.description.affiliation | Univ Estadual Paulista, Fac Ciências Farmaceut, Dept Principios At & Nat, Araraquara, SP, Brazil | - |
dc.description.affiliationUnesp | Univ Estadual Paulista, Dept Quim, Fac Ciências, Bauru, Brazil | - |
dc.description.affiliationUnesp | Univ Estadual Paulista, Fac Ciências Farmaceut, Dept Principios At & Nat, Araraquara, SP, Brazil | - |
dc.identifier.doi | 10.1111/j.1600-076X.2007.00419.x | - |
dc.identifier.wos | WOS:000245405200011 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Journal of Pineal Research | - |
Aparece nas coleções: | Artigos, TCCs, Teses e Dissertações da Unesp |
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