Transcriptional regulators ChlR and CnfR are essential for diazotrophic growth in nonheterocystous cyanobacteria

Proc Natl Acad Sci U S A. 2014 May 6;111(18):6762-7. doi: 10.1073/pnas.1323570111. Epub 2014 Apr 21.

Abstract

Leptolyngbya boryana (Plectonema boryanum) is a diazotrophic cyanobacterium lacking heterocysts. How nitrogen fixation is regulated in filamentous nonheterocystous cyanobacteria remains unclear. Here we describe a large 50-kb nitrogen fixation (nif) gene cluster in L. boryana containing 50 genes. This gene cluster contains 14 nif genes (nifBSUHDKVZT and nifPENXW), two genes encoding transcriptional regulators showing high similarity to ChlR (chlorophyll regulator) and PatB, three genes encoding ferredoxin, three genes encoding cytochrome oxidase subunits, and 28 genes encoding nif-related proteins and proteins with putative or unknown functions. Eleven mutants lacking one gene or a subset of genes were isolated. Five of them did not grow under diazotrophic conditions, including two mutants lacking the transcriptional regulators. Although the chlR homolog-lacking mutant showed a normal level of nitrogenase activity, various intermediates of chlorophyll biosynthesis were accumulated under micro-oxic conditions. The phenotype suggested that ChlR activates the expression of the genes responsible for anaerobic chlorophyll biosynthesis to support energy supply for nitrogen fixation. In another mutant lacking the patB homolog, no transcripts of any nif genes were detected under nitrogen fixation conditions, which was consistent with no activity. Constitutive expression of patB in a shuttle vector resulted in low but significant nitrogenase activity even under nitrate-replete conditions, suggesting that the PatB homolog is the master regulator of nitrogen fixation. We propose to rename the patB homolog as cnfR, after cyanobacterial nitrogen fixation regulator.

Keywords: anoxia-induced expression; iron–sulfur cluster.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism*
  • Base Sequence
  • Chlorophyll / metabolism
  • DNA, Bacterial / genetics
  • Genes, Bacterial*
  • Models, Biological
  • Molecular Sequence Data
  • Multigene Family*
  • Mutation
  • Nitrogen Fixation / genetics
  • Nitrogenase / genetics
  • Nitrogenase / metabolism
  • Plectonema / genetics*
  • Plectonema / growth & development
  • Plectonema / metabolism*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism*

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Transcription Factors
  • Chlorophyll
  • Nitrogenase

Associated data

  • GENBANK/AB808482
  • GENBANK/AB808629
  • GENBANK/AB808630