On the two iron centers of desulfoferrodoxin

FEBS Lett. 1993 Dec 20;336(1):13-8. doi: 10.1016/0014-5793(93)81599-u.

Abstract

Desulfoferrodoxin from Desulfovibrio vulgaris, strain Hildenborough, is a homodimer of 28 kDa; it contains two Fe atoms per 14.0 kDa subunit. The N-terminal amino-acid sequence is homogeneous and corresponds to the previously described Rho gene, which encodes a highly charged 14 kDa polypeptide without a leader sequence. Although one of the two iron centers, FeA, has previously been described as a 'strained rubredoxin-like' site, EPR of the ferric form proves very similar to that of the pentagonal bipyramidally coordinated iron in ferric complexes of DTPA, diethylenetriaminepentaacetic acid: both systems have spin S = 5/2 and rhombicity E/D = 0.08. Unlike the Fe site in rubredoxin the FeA site in desulfoferrodoxin has a pH dependent midpoint potential with pKox = 9.2 and pKred = 5.3. Upon reduction (Em,7.5 = +2 mV) FeA exhibits an unusually sharp S = 2 resonance in parallel-mode EPR. The second iron, FeB, has S = 5/2 and E/D = 0.33; upon reduction (Em,7.5 = +90 mV) FeB turns EPR-silent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antibodies
  • Desulfovibrio vulgaris / chemistry
  • Electrochemistry
  • Electron Spin Resonance Spectroscopy
  • Ferredoxins / chemistry*
  • Ferredoxins / immunology
  • Iron / chemistry*
  • Molecular Sequence Data
  • Oxidation-Reduction

Substances

  • Antibodies
  • Ferredoxins
  • desulfoferrodoxin
  • Iron