A 12-cistron Escherichia coli operon (hyf) encoding a putative proton-translocating formate hydrogenlyase system

  • Simon C. Andrews
    The Krebs Institute, Department of Molecular Biology & Biotechnology, Western Bank, Firth Court, University of Sheffield, Sheffield S10 2TN, UK
  • Ben C. Berks
    The Centre for Metalloprotein Spectroscopy & Biology, School of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, UK
  • Joseph McClay
    The Sanger Centre, Hinxton Hall, Hinxton, Cambridge CB10 1SB, UK
  • Andrew Ambler
    The Sanger Centre, Hinxton Hall, Hinxton, Cambridge CB10 1SB, UK
  • Michael A. Quail
    The Krebs Institute, Department of Molecular Biology & Biotechnology, Western Bank, Firth Court, University of Sheffield, Sheffield S10 2TN, UK
  • Paul Golby
    The Krebs Institute, Department of Molecular Biology & Biotechnology, Western Bank, Firth Court, University of Sheffield, Sheffield S10 2TN, UK
  • John R. Guest
    The Krebs Institute, Department of Molecular Biology & Biotechnology, Western Bank, Firth Court, University of Sheffield, Sheffield S10 2TN, UK

抄録

<jats:p>The nucleotide sequence has been determined for a twelve-gene operon of<jats:italic>Escherichia coli</jats:italic>designated the<jats:italic>hyf</jats:italic>operon (<jats:italic>hyfABCDEFGHIR-focB</jats:italic>). The<jats:italic>hyf</jats:italic>operon is located at 55.8-56.0 min and encodes a putative nine-subunit hydrogenase complex (hydrogenase four or Hyf), a potential formate- and σ<jats:sup>54</jats:sup>dependent transcriptional activator, HyfR (related to FhlA), and a possible formate transporter, FocB (related to FocA). Five of the nine Hyf-complex subunits are related to subunits of both the<jats:italic>E. coli</jats:italic>hydrogenase-3 complex (Hyc) and the proton-translocating NADH:quinone oxidoreductases (complex I and Nuo), whereas two Hyf subunits are related solely to NADH:quinone oxidoreductase subunits. The Hyf components include a predicted 523 residue [Ni-Fe] hydrogenase (large subunit) with an N-terminus (residues 1-170) homologous to the 30 kDa or NuoC subunit of complex I. It is proposed that Hyf, in conjunction with formate dehydrogenase H (Fdh-H), forms a hitherto unrecognized respiration-linked proton-translocating formate hydrogenlyase (FHL-2). It is likely that HyfR acts as a formate-dependent regulator of the<jats:italic>hyf</jats:italic>operon and that FocB provides the Hyf complex with external formate as substrate.</jats:p>

収録刊行物

  • Microbiology

    Microbiology 143 (11), 3633-3647, 1997-11-01

    Microbiology Society

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