Literature DB >> 15571216

EPR spin trapping of a radical intermediate in the urate oxidase reaction.

E Busi1, L Terzuoli, R Basosi, B Porcelli, E Marinello.   

Abstract

Urate oxidase, or uricase (EC 1.7.3.3), is a peroxisomal enzyme that catalyses the oxidation of uric acid to allantoin. The chemical mechanism of the urate oxidase reaction has not been clearly established, but the involvement of radical intermediates was hypothesised. In this study EPR spectroscopy by spin trapping of radical intermediates has been used in order to demonstrate the eventual presence of radical transient urate species. The oxidation reaction of uric acid by several uricases (Porcine Liver, Bacillus Fastidiosus, Candida Utilitis) was performed in the presence of 5-diethoxyphosphoryl-5-methyl-pyrroline-N-oxide (DEPMPO) as spin trap. DEPMPO was added to reaction mixture and a radical adduct was observed in all cases. Therefore, for the first time, the presence of a radical intermediate in the uricase reaction was experimentally proved.

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Year:  2004        PMID: 15571216     DOI: 10.1081/NCN-200027390

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  2 in total

1.  Structural and mechanistic studies of HpxO, a novel flavin adenine dinucleotide-dependent urate oxidase from Klebsiella pneumoniae.

Authors:  Katherine A Hicks; Seán E O'Leary; Tadhg P Begley; Steven E Ealick
Journal:  Biochemistry       Date:  2013-01-09       Impact factor: 3.162

2.  Biochemical characterization of the HpxO enzyme from Klebsiella pneumoniae, a novel FAD-dependent urate oxidase.

Authors:  Seán E O'Leary; Katherine A Hicks; Steven E Ealick; Tadhg P Begley
Journal:  Biochemistry       Date:  2009-04-14       Impact factor: 3.162

  2 in total

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