A novel type of nitric-oxide reductase: Escherichia coli flavorubredoxin (Articolo in rivista)

Type
Label
  • A novel type of nitric-oxide reductase: Escherichia coli flavorubredoxin (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1074/jbc.M203886200 (literal)
Alternative label
  • Gomes, Cláudio M.; Giuffrè, Alessandro; Forte, Elena; Vicente, João B.; Saraiva, Lígia M.; Brunori, Maurizio; Teixeira, Miguel Sepúlveda (2002)
    A novel type of nitric-oxide reductase: Escherichia coli flavorubredoxin
    in The Journal of biological chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Gomes, Cláudio M.; Giuffrè, Alessandro; Forte, Elena; Vicente, João B.; Saraiva, Lígia M.; Brunori, Maurizio; Teixeira, Miguel Sepúlveda (literal)
Pagina inizio
  • 25273 (literal)
Pagina fine
  • 25276 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/record/display.url?eid=2-s2.0-0037067737&origin=inward (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 277 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 28 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Instituto de Tecnologia Quimica e Biologica - Univesidade Nova de Lisboa; Faculdade de Ciencias e Tecnologia, New University of Lisbon; Universita degli Studi di Roma La Sapienza (literal)
Titolo
  • A novel type of nitric-oxide reductase: Escherichia coli flavorubredoxin (literal)
Abstract
  • Escherichia coli flavorubredoxin is a member of the family of the A-type flavoproteins, which are built by two core domains: a metallo-beta-lactamase-like domain, at the N-terminal region, harboring a non-heme di-iron site, and a flavodoxin-like domain, containing one FMN moiety. The enzyme from E. coli has an extra module at the C terminus, containing a rubredoxin-like center. The A-type flavoproteins are widespread among strict and facultative anaerobes, as deduced from the analysis of the complete prokaryotic genomes. In this report we showed that the recombinant enzyme purified from E. coli has nitric-oxide reductase activity with a turnover number of approximately 15 mol of NO.mol enzyme(-1).s(-1), which was well within the range of those determined for the canonical heme b(3)-Fe(B) containing nitric-oxide reductases (e.g. approximately 10-50 mol NO.mol enzyme(-1).s(-1) for the Paracoccus denitrificans NOR). Furthermore, it was shown that the activity was due to the A-type flavoprotein core, as the rubredoxin domain alone exhibited no activity. Thus, a novel family of prokaryotic NO reductases, with a non-heme di-iron site as the catalytic center, was established. (literal)
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