Nitrogenase expression in estuarine bacterioplankton influenced by organic carbon and availability of oxygen

FEMS Microbiol Lett. 2015 Jul;362(14):fnv105. doi: 10.1093/femsle/fnv105. Epub 2015 Jul 6.

Abstract

The genetic capacity to fix gaseous nitrogen (N) is distributed among diverse diazotrophs belonging to the Bacteria and Archaea. However, only a subset of the putative diazotrophs present actively fix N at any given time in the environment. We experimentally tested whether the availability of carbon and inhibition by oxygen constrain N fixation by diazotrophs in coastal seawater. The goal was to test whether by alleviating these constraints an increased overlap between nitrogenase (nifH)-gene-carrying and -expressing organisms could be achieved. We incubated water from a eutrophic but N-limited fjord in Denmark under high-carbon/low-oxygen conditions and determined bacterial growth and production, diazotrophic community composition (Illumina nifH amplicon sequencing), and nifH gene abundance and expression [quantitative PCR (qPCR) and quantitative reverse transcriptase PCR (qRT-PCR)]. Bacterial abundances and production increased under high-carbon/low-oxygen conditions as did the similarity between present and active diazotrophic communities. This was caused by the loss of specific abundant yet non-active gammaproteobacterial phylotypes and increased expression by others. The prominent active gamma- and epsilonproteobacterial diazotrophs did not, however, respond to these conditions in a uniform way, highlighting the difficulty to assess how a change in environmental conditions may affect a diverse indigenous diazotrophic community.

Keywords: bacterial activity; limiting factors; nitrogen fixation.

Publication types

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

MeSH terms

  • Bacteria / genetics*
  • Carbon / metabolism*
  • Epsilonproteobacteria / genetics
  • Epsilonproteobacteria / physiology
  • Estuaries*
  • Gammaproteobacteria / genetics
  • Gammaproteobacteria / physiology
  • Microbial Consortia / physiology*
  • Nitrogen Fixation*
  • Nitrogenase / genetics*
  • Oxidoreductases / genetics
  • Oxygen / metabolism*
  • Phylogeny
  • Plankton / genetics*
  • Plankton / physiology
  • Real-Time Polymerase Chain Reaction
  • Seawater / microbiology

Substances

  • Carbon
  • Oxidoreductases
  • Nitrogenase
  • nitrogenase reductase
  • Oxygen