Elevated CO2 differentially regulates root nitrate transporter kinetics in a genotype and nitrate dose-dependent manner

Plant Sci. 2021 Apr:305:110807. doi: 10.1016/j.plantsci.2020.110807. Epub 2021 Jan 13.

Abstract

The nitrogen (N) and protein concentration of wheat crop and grain often decline as a result of exposure of the crop to elevated CO2 (EC). In our earlier studies, it was found that the exacerbated production of nitric oxide (NO) represses the transcription of nitrate reductase (NR) and high affinity nitrate transporters (HATS) in EC grown wheat seedlings receiving high N. High N supply under EC also resulted in accumulation of reactive oxygen species (ROS), and reactive nitrogen species (RNS; NO and S- nitrosothiols) ensuing faster senescence and reduced N metabolite concentration in wheat. In this study, the effect of short-term exposure to EC on nitrate uptake kinetics was studied. The impact of EC on constitutive and inducible components of high affinity and low affinity nitrate uptake systems (HATS and LATS) were delineated in two wheat genotypes diverse in terms of nitrate uptake and assimilation capacities. Nitrate dose-response of NR was suppressed by EC in both leaf and root tissues. Plants grown under EC displayed a marked reduction in nitrate uptake kinetic components of LATS. Wheat genotype with high leaf nitrate assimilation capacity was able to maintain considerably higher nitrate uptake rate under EC albeit at a lower rate in comparison to ambient CO2. Wheat leaves exposed to EC displayed a comparatively higher abundance of NO and showed incremental abundance depending on increase in nitrate supply. Exogenous NO supply significantly suppressed the nitrate uptake rate of EC grown plants. Hence, EC-induced production of NO downregulates LATS kinetics in a genotype and nitrate dose-dependent manner.

Keywords: Elevated CO(2); High affinity nitrate transport system; K(m); Low affinity nitrate transport system; Nitrate uptake kinetics; V(max); Wheat.

Publication types

  • Comparative Study

MeSH terms

  • Anion Transport Proteins / genetics*
  • Anion Transport Proteins / metabolism*
  • Carbon Dioxide / metabolism*
  • Crops, Agricultural / genetics
  • Crops, Agricultural / metabolism
  • Genetic Variation
  • Genotype
  • Kinetics
  • Nitrates / metabolism*
  • Nitric Oxide / metabolism
  • Plant Leaves / metabolism
  • Plant Roots / metabolism*
  • Seedlings / metabolism
  • Triticum / genetics*
  • Triticum / metabolism*

Substances

  • Anion Transport Proteins
  • Nitrates
  • Carbon Dioxide
  • Nitric Oxide