A paramagnetic species with unique EPR characteristics in the active site of heterodisulfide reductase from methanogenic archaea

Eur J Biochem. 2001 May;268(9):2566-77. doi: 10.1046/j.1432-1327.2001.02141.x.

Abstract

Heterodisulfide reductase (Hdr) from methanogenic archaea is an iron-sulfur protein that catalyses the reversible reduction of the heterodisulfide (CoM-S-S-CoB) of the methanogenic thiol coenzymes, coenzyme M (H-S-CoM) and coenzyme B (H-S-CoB). In EPR spectroscopic studies with the enzyme from Methanothermobacter marburgensis, we have identified a unique paramagnetic species that is formed upon reaction of the oxidized enzyme with H-S-CoM in the absence of H-S-CoB. This paramagnetic species can be reduced in a one-electron step with a midpoint-potential of -185 mV but not further oxidized. A broadening of the EPR signal in the 57Fe-enriched enzyme indicates that it is at least partially iron based. The g values (gxyz = 2.013, 1.991 and 1.938) and the midpoint potential argue against a conventional [2Fe-2S]+, [3Fe-4S]+, [4Fe-4S]+ or [4Fe-4S]3+ cluster. This species reacts with H-S-CoB to form an EPR silent form. Hence, we propose that only a half reaction is catalysed in the presence of H-S-CoM and that a reaction intermediate is trapped. This reaction intermediate is thought to be a [4Fe-4S]3+ cluster that is coordinated by one of the cysteines of a nearby active-site disulfide or by the sulfur of H-S-CoM. A paramagnetic species with similar EPR properties was also identified in Hdr from Methanosarcina barkeri.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylating Agents / pharmacology
  • Amino Acid Sequence
  • Base Sequence
  • Catalytic Domain
  • DNA Primers / genetics
  • Electron Spin Resonance Spectroscopy
  • Enzyme Inhibitors / pharmacology
  • Euryarchaeota / enzymology*
  • Euryarchaeota / genetics
  • Methanobacterium / enzymology
  • Methanobacterium / genetics
  • Methanosarcina barkeri / enzymology
  • Methanosarcina barkeri / genetics
  • Oxidation-Reduction
  • Oxidoreductases / antagonists & inhibitors
  • Oxidoreductases / chemistry*
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Phosphothreonine / analogs & derivatives*
  • Phosphothreonine / chemistry
  • Protein Subunits
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics

Substances

  • Alkylating Agents
  • DNA Primers
  • Enzyme Inhibitors
  • Protein Subunits
  • Recombinant Proteins
  • 7-mercaptoheptanoylthreonine phosphate
  • Phosphothreonine
  • Oxidoreductases
  • coenzyme M-7-merceptoheptanoylthreonine-phosphate-heterodisulfide hydrogenase
  • heterodisulfide reductase