Potassium alleviates ammonium toxicity in rice by reducing its uptake through activation of plasma membrane H+-ATPase to enhance proton extrusion

Plant Physiol Biochem. 2020 Jun:151:429-437. doi: 10.1016/j.plaphy.2020.03.040. Epub 2020 Apr 2.

Abstract

Potassium (K+) has been reported to alleviate ammonium (NH4+) toxicity in rice through some underlying mechanisms, but it still not clear. In addition, K+ is an important cation for activation of plasma membrane (PM) H+-ATPase activity. Here, we hypothesized that K+ alleviated NH4+ toxicity by mediating PM H+-ATPase function in rice root. In this study, rice plants were cultivated in hydroponic solution with various concentrations of K+ and NH4+. By concurrently supplying K+ with NH4+ or re-supplying K+ after NH4+ toxicity, we found that high K+ concentration reduced the NH4+ uptake rate, enhanced the H+ extrusion rate by the roots, and alleviated rice NH4+ toxicity. The gene expression levels of PM H+-ATPase members (OsA1, 3, 7, 8, and 9) were upregulated by application of increasing concentrations of K+ under NH4+ toxicity. The PM H+-ATPase activity and protein expression in rice roots were also enhanced. Furthermore, the enhancement of PM H+-ATPase activity by a specific stimulator (fusicoccin) rescued rice seedlings from NH4+ toxicity. Taken together, these results indicate that K+ can alleviate NH4+ toxicity, possibly by activating PM H+-ATPase to extrude more H+ and inhibit NH4+ uptake by root. Our results may enhance understanding of the strategy of applying K+ fertilizer to mitigate crop NH4+ toxicity in agriculture.

Keywords: Ammonium; Plasma membrane H(+)-ATPase; Potassium; Proton extrusion; Rice; Root.

MeSH terms

  • Ammonium Compounds* / metabolism
  • Ammonium Compounds* / toxicity
  • Cell Membrane / drug effects
  • Cell Membrane / enzymology
  • Enzyme Activation / drug effects
  • Oryza* / drug effects
  • Oryza* / enzymology
  • Plant Roots / drug effects
  • Plant Roots / enzymology
  • Potassium* / pharmacology
  • Proton-Translocating ATPases* / metabolism

Substances

  • Ammonium Compounds
  • Proton-Translocating ATPases
  • Potassium