Direct electrochemistry of two genetically distinct flavodoxins isolated from Azotobacter chroococcum grown under nitrogen-fixing conditions

Biochem J. 1991 Jul 15;277 ( Pt 2)(Pt 2):313-9. doi: 10.1042/bj2770313.

Abstract

Two genetically distinct flavodoxins, designated AcFldA and AcFldB, were isolated from Azotobacter chroococcum (MCD1155) grown under nitrogen-fixing conditions. AcFldA and AcFldB differ in their midpoint potentials for the semiquinone-hydroquinone couple (Em -305 mV and -520 mV respectively). Only AcFldB was competent to act as an electron donor to the Mo-containing nitrogenase of A. chroococcum. The N-terminal amino acid sequence (20 residues) of AcFldB was identical with that predicted from the nifF DNA sequence of A. vinelandii OP [Bennett, Jacobsen & Dean (1988) J. Biol. Chem. 263, 1364-1369], suggesting that AcFldB is the nifF gene product of A. chroococcum (MCD1155). Direct fast reversible electrochemistry of these flavodoxins has been achieved at a polished edge-plane graphite electrode using the aminoglycoside neomycin as a promoter. The heterogeneous rates of electron transfer between the graphite electrode and AcFldA and AcFldB were determined to be 1.2 x 10(-3) cm.s-1 and 2.0 x 10(-3) cm.s-1 respectively. The natures of two minor species of flavodoxin designated AcFldC and AcFldD, which were resolved by f.p.l.c., are also discussed.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Azotobacter / genetics
  • Azotobacter / growth & development
  • Azotobacter / metabolism*
  • Chromatography, High Pressure Liquid
  • DNA, Bacterial / genetics
  • Electrochemistry
  • Flavodoxin / chemistry
  • Flavodoxin / genetics*
  • Flavodoxin / isolation & purification
  • Genes, Bacterial*
  • Molecular Sequence Data
  • Nitrogen Fixation / genetics*
  • Peptide Mapping
  • Spectrophotometry

Substances

  • DNA, Bacterial
  • Flavodoxin