Nitrogen-Fixing Nodules Are an Important Source of Reduced Sulfur, Which Triggers Global Changes in Sulfur Metabolism in Lotus japonicus

Plant Cell. 2015 Sep;27(9):2384-400. doi: 10.1105/tpc.15.00108. Epub 2015 Aug 21.

Abstract

We combined transcriptomic and biochemical approaches to study rhizobial and plant sulfur (S) metabolism in nitrogen (N) fixing nodules (Fix(+)) of Lotus japonicus, as well as the link of S-metabolism to symbiotic nitrogen fixation and the effect of nodules on whole-plant S-partitioning and metabolism. Our data reveal that N-fixing nodules are thiol-rich organs. Their high adenosine 5'-phosphosulfate reductase activity and strong (35)S-flux into cysteine and its metabolites, in combination with the transcriptional upregulation of several rhizobial and plant genes involved in S-assimilation, highlight the function of nodules as an important site of S-assimilation. The higher thiol content observed in nonsymbiotic organs of N-fixing plants in comparison to uninoculated plants could not be attributed to local biosynthesis, indicating that nodules are an important source of reduced S for the plant, which triggers whole-plant reprogramming of S-metabolism. Enhanced thiol biosynthesis in nodules and their impact on the whole-plant S-economy are dampened in plants nodulated by Fix(-) mutant rhizobia, which in most respects metabolically resemble uninoculated plants, indicating a strong interdependency between N-fixation and S-assimilation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Gene Expression Regulation, Plant
  • Lotus / genetics
  • Lotus / metabolism*
  • Lotus / physiology
  • Mesorhizobium / genetics
  • Mesorhizobium / physiology
  • Nitrogen Fixation
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Oxidoreductases Acting on Sulfur Group Donors / metabolism
  • Plant Proteins / metabolism
  • Root Nodules, Plant / metabolism*
  • Root Nodules, Plant / microbiology*
  • Sulfhydryl Compounds / metabolism
  • Sulfur / metabolism*
  • Sulfur Radioisotopes / metabolism
  • Sulfur Radioisotopes / pharmacokinetics
  • Symbiosis
  • Tissue Distribution
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Bacterial Proteins
  • NifA protein, Bacteria
  • Plant Proteins
  • Sulfhydryl Compounds
  • Sulfur Radioisotopes
  • Transcription Factors
  • Sulfur
  • Oxidoreductases
  • nitrogenase reductase
  • Oxidoreductases Acting on Sulfur Group Donors
  • adenylylsulfate reductase