Cool C4 photosynthesis: pyruvate Pi dikinase expression and activity corresponds to the exceptional cold tolerance of carbon assimilation in Miscanthus x giganteus

Plant Physiol. 2008 Sep;148(1):557-67. doi: 10.1104/pp.108.120709. Epub 2008 Jun 6.

Abstract

The bioenergy feedstock grass Miscanthus x giganteus is exceptional among C(4) species for its high productivity in cold climates. It can maintain photosynthetically active leaves at temperatures 6 degrees C below the minimum for maize (Zea mays), which allows it a longer growing season in cool climates. Understanding the basis for this difference between these two closely related plants may be critical in adapting maize to colder weather. When M. x giganteus and maize grown at 25 degrees C were transferred to 14 degrees C, light-saturated CO(2) assimilation and quantum yield of photosystem II declined by 30% and 40%, respectively, in the first 48 h in these two species. The decline continued in maize but arrested and then recovered partially in M. x giganteus. Within 24 h of the temperature transition, the pyruvate phosphate dikinase (PPDK) protein content per leaf area transiently declined in M. x giganteus but then steadily increased, such that after 7 d the enzyme content was significantly higher than in leaves growing in 25 degrees C. By contrast it declined throughout the chilling period in maize leaves. Rubisco levels remained constant in M. x giganteus but declined in maize. Consistent with increased PPDK protein content, the extractable PPDK activity per unit leaf area (V(max)(,ppdk)) in cold-grown M. x giganteus leaves was higher than in warm-grown leaves, while V(max,ppdk) was lower in cold-grown than in warm-grown maize. The rate of light activation of PPDK was also slower in cold-grown maize than M. x giganteus. The energy of activation (E(a)) of extracted PPDK was lower in cold-grown than warm-grown M. x giganteus but not in maize. The specific activities and E(a) of purified recombinant PPDK from M. x giganteus and maize cloned into Escherichia coli were similar. The increase in PPDK protein in the M. x giganteus leaves corresponded to an increase in PPDK mRNA level. These results indicate that of the two enzymes known to limit C(4) photosynthesis, increase of PPDK, not Rubisco content, corresponds to the recovery and maintenance of photosynthetic capacity. Functionally, increased enzyme concentration is shown to increase stability of M. x giganteus PPDK at low temperature. The results suggest that increases in either PPDK RNA transcription and/or the stability of this RNA are important for the increase in PPDK protein content and activity in M. x giganteus under chilling conditions relative to maize.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbon Dioxide / metabolism
  • Chlorophyll / metabolism
  • Cold Temperature*
  • Enzyme Activation
  • Kinetics
  • Light
  • Photosynthesis*
  • Photosystem II Protein Complex / metabolism
  • Plant Leaves / metabolism
  • Poaceae / metabolism*
  • Pyruvate, Orthophosphate Dikinase / metabolism*
  • Recombinant Proteins / metabolism
  • Zea mays / metabolism*

Substances

  • Photosystem II Protein Complex
  • Recombinant Proteins
  • Chlorophyll
  • Carbon Dioxide
  • Pyruvate, Orthophosphate Dikinase