The novel regulatory ncRNA, NfiS, optimizes nitrogen fixation via base pairing with the nitrogenase gene nifK mRNA in Pseudomonas stutzeri A1501

Proc Natl Acad Sci U S A. 2016 Jul 26;113(30):E4348-56. doi: 10.1073/pnas.1604514113. Epub 2016 Jul 12.

Abstract

Unlike most Pseudomonas, the root-associated bacterium Pseudomonas stutzeri A1501 fixes nitrogen after the horizontal acquisition of a nitrogen-fixing (nif) island. A genome-wide search for small noncoding RNAs (ncRNAs) in P. stutzeri A1501 identified the novel P. stutzeri-specific ncRNA NfiS in the core genome, whose synthesis was significantly induced under nitrogen fixation or sorbitol stress conditions. The expression of NfiS was RNA chaperone Hfq-dependent and activated by the sigma factor RpoN/global nitrogen activator NtrC/nif-specific activator NifA regulatory cascade. The nfiS-deficient mutant displayed reduced nitrogenase activity, as well as increased sensitivity to multiple stresses, such as osmotic and oxidative stresses. Secondary structure prediction and complementation studies confirmed that a stem-loop structure was essential for NfiS to regulate the nitrogenase gene nifK mRNA synthesis and thus nitrogenase activity. Microscale thermophoresis and physiological analysis showed that NfiS directly pairs with nifK mRNA and ultimately enhances nitrogenase activity by increasing the translation efficiency and the half-life of nifK mRNA. Our data also suggest structural and functional divergence of NfiS evolution in diazotrophic and nondiazotrophic backgrounds. It is proposed that NfiS was recruited by nifK mRNA as a novel regulator to integrate the horizontally acquired nif island into host global networks.

Keywords: NfiS; Pseudomonas stutzeri; nifK mRNA; nitrogen fixation; regulatory ncRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Base Pairing / genetics*
  • Base Sequence
  • Gene Expression Regulation, Bacterial
  • Mutation
  • Nitrogen Fixation / genetics*
  • Nitrogenase / genetics*
  • Nitrogenase / metabolism
  • Nucleic Acid Conformation
  • Pseudomonas stutzeri / genetics*
  • Pseudomonas stutzeri / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Untranslated / chemistry
  • RNA, Untranslated / genetics*
  • Sequence Homology, Nucleic Acid

Substances

  • Bacterial Proteins
  • RNA, Messenger
  • RNA, Untranslated
  • Nitrogenase