Regulation of C4 photosynthesis: purification and properties of the protein catalyzing ADP-mediated inactivation and Pi-mediated activation of pyruvate,Pi dikinase

Arch Biochem Biophys. 1985 Mar;237(2):490-503. doi: 10.1016/0003-9861(85)90302-9.


Pyruvate,Pi dikinase regulatory protein (PDRP) has been highly purified from maize leaves, and its role in catalyzing both ADP-mediated inactivation (due to phosphorylation of a threonine residue) and Pi-mediated activation (due to dephosphorylation by phosphorolysis) of pyruvate,Pi dikinase has been confirmed. These reactions account for the dark/light-mediated regulation of pyruvate,Pi dikinase observed in the leaves of C4 plants. During purification to apparent homogeneity the ratio of these two activities remained constant. The molecular weight of the native PDRP was about 180,000 at pH 8.3 and 90,000 at pH 7.5. Its monomeric molecular weight was 45,000. It was confirmed that inactive pyruvate,Pi dikinase free of a phosphate group on a catalytic histidine was the preferred substrate for activation. Michaelis constants for orthophosphate and the above form of active pyruvate,Pi dikinase were determined, as well as the mechanism of inhibition of the PDRP-catalyzed reaction by ATP, ADP, AMP, and PPi. For the inactivation reaction, Km values were 1.2 microM for the active pyruvate,Pi dikinase and 52 microM for ADP. CDP and GDP but not UDP could substitute for ADP. The inactivation reaction is inhibited by inactive pyruvate,Pi dikinase competitively with respect to both active pyruvate,Pi dikinase and ADP. Both the activation and inactivation reactions catalyzed by PDRP have a broad pH optimum between 7.8 and 8.3. The results are discussed in terms of the likely mechanism of dark/light regulation of pyruvate,Pi dikinase in vivo.

MeSH terms

  • Adenosine Diphosphate / analogs & derivatives
  • Adenosine Diphosphate / pharmacology
  • Adenosine Diphosphate / physiology*
  • Adenosine Monophosphate / pharmacology
  • Catalysis
  • Chemical Phenomena
  • Chemistry
  • Enzyme Activation
  • Hydrogen-Ion Concentration
  • Kinetics
  • Molecular Weight
  • Phosphotransferases / metabolism*
  • Photosynthesis*
  • Plant Proteins / antagonists & inhibitors
  • Plant Proteins / isolation & purification*
  • Plant Proteins / physiology
  • Pyruvate, Orthophosphate Dikinase / antagonists & inhibitors
  • Pyruvate, Orthophosphate Dikinase / metabolism*
  • Substrate Specificity
  • Zea mays / metabolism


  • Plant Proteins
  • Adenosine Monophosphate
  • Adenosine Diphosphate
  • Phosphotransferases
  • PPDK protein, Zea mays
  • Pyruvate, Orthophosphate Dikinase