Electron uptake by iron-oxidizing phototrophic bacteria

Nat Commun. 2014 Feb 26:5:3391. doi: 10.1038/ncomms4391.

Abstract

Oxidation-reduction reactions underlie energy generation in nearly all life forms. Although most organisms use soluble oxidants and reductants, some microbes can access solid-phase materials as electron-acceptors or -donors via extracellular electron transfer. Many studies have focused on the reduction of solid-phase oxidants. Far less is known about electron uptake via microbial extracellular electron transfer, and almost nothing is known about the associated mechanisms. Here we show that the iron-oxidizing photoautotroph Rhodopseudomonas palustris TIE-1 accepts electrons from a poised electrode, with carbon dioxide as the sole carbon source/electron acceptor. Both electron uptake and ruBisCo form I expression are stimulated by light. Electron uptake also occurs in the dark, uncoupled from photosynthesis. Notably, the pioABC operon, which encodes a protein system essential for photoautotrophic growth by ferrous iron oxidation, influences electron uptake. These data reveal a previously unknown metabolic versatility of photoferrotrophs to use extracellular electron transfer for electron uptake.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Carbon Dioxide / metabolism*
  • Electrochemical Techniques / instrumentation
  • Electrochemical Techniques / methods
  • Electrodes / microbiology
  • Electron Transport / radiation effects
  • Electrons*
  • Gene Expression Regulation, Bacterial / radiation effects
  • Iron / metabolism*
  • Light
  • Microbial Viability / genetics
  • Microbial Viability / radiation effects
  • Microscopy, Electron, Scanning
  • Microscopy, Fluorescence
  • Mutation
  • Oxidation-Reduction / radiation effects
  • Photosynthesis / radiation effects
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rhodopseudomonas / genetics
  • Rhodopseudomonas / metabolism*
  • Rhodopseudomonas / ultrastructure
  • Ribulose-Bisphosphate Carboxylase / genetics
  • Ribulose-Bisphosphate Carboxylase / metabolism

Substances

  • Bacterial Proteins
  • Carbon Dioxide
  • Adenosine Triphosphate
  • Iron
  • Ribulose-Bisphosphate Carboxylase