Abstract

Introduction of a C4 photosynthetic pathway into C3 rice (Oryza sativa) requires installation of a biochemical pump that concentrates CO2 at the site of carboxylation in modified bundle sheath cells. To investigate the feasibility of this, we generated a quadruple line that simultaneously accumulates four of the core C4 photosynthetic enzymes from the NADP-malic enzyme subtype, phosphoenolpyruvate carboxylase (ZmPEPC), NADP-malate dehydrogenase (ZmNADP-MDH), NADP-malic enzyme (ZmNADP-ME), and pyruvate phosphate dikinase (ZmPPDK). This led to enhanced enzyme activity and mild phenotypic perturbations but was largely neutral in its effects on photosynthetic rate. Measurements of the flux of 13CO2 through photosynthetic metabolism revealed a significant increase in the incorporation of 13C into malate, consistent with increased fixation of 13CO2 via PEP carboxylase in lines expressing the maize PEPC enzyme. However, there was no significant differences in labeling of 3-phosphoglycerate (3PGA) indicating that there was no carbon flux through NADP-ME into the Calvin-Benson cycle. There was also no significant difference in labeling of phosphoenolpyruvate (PEP) indicating that there was no carbon flux through PPDK. Crossing the quadruple line with a line with reduced glycine decarboxylase H-protein (OsGDCH) abundance led to a photosynthetic phenotype characteristic of the reduced OsGDCH line and higher labeling of malate, aspartate and citrate than in the quintuple line. There was evidence of 13C labeling of aspartate indicating 13CO2 fixation into oxaloacetate by PEPC and conversion to aspartate by the endogenous aspartate aminotransferase activity. While Kranz anatomy or other anatomical modifications have not yet been installed in these plants to enable a fully functional C4 cycle, these results demonstrate for the first-time a partial flux through the carboxylation phase of NADP-ME C4 metabolism in transgenic rice containing two of the key metabolic steps in the C4 pathway.

Highlights

  • Introduction of aC4 photosynthetic pathway into C3 rice (Oryza sativa) requires installation of a biochemical pump that concentrates CO2 at the site of carboxylation in modified bundle sheath cells

  • CO2 is assimilated by ribulose bisphosphate carboxylase/oxygenase (Rubisco), yielding two molecules of 3PGA, about half of which is reduced to triose-phosphate (TPs) using the NADPH provided by NADP-dependent malic enzyme (NADP-ME) in the bundle sheath cells (BSCs) chloroplast to regenerate RuBP in the Calvin-Benson cycle

  • Immunoblotting of F2 generation transgenic plants showed that the protein of the correct size for ZmPEPC, ZmNADPMDH, ZmNADP-ME, and ZmPPDK was stably expressed in both the quadruple and quintuple cross rice lines, with OsGDCH protein almost undetectable in the quintuple cross (Figure 1)

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Summary

Introduction

Introduction of aC4 photosynthetic pathway into C3 rice (Oryza sativa) requires installation of a biochemical pump that concentrates CO2 at the site of carboxylation in modified bundle sheath cells. To investigate the feasibility of this, we generated a quadruple line that simultaneously accumulates four of the core C4 photosynthetic enzymes from the NADP-malic enzyme subtype, phosphoenolpyruvate carboxylase (ZmPEPC), NADP-malate dehydrogenase (ZmNADP-MDH), NADP-malic enzyme (ZmNADP-ME), and pyruvate phosphate dikinase (ZmPPDK). This led to enhanced enzyme activity and mild phenotypic perturbations but was largely neutral in its effects on photosynthetic rate. In the majority of C4 plants, this is achieved by compartmentalization of photosynthetic reactions between two morphologically distinct cell types: the mesophyll cells (MCs) and the bundle sheath cells (BSCs) Operating across these cells is a biochemical CO2 pump elevating the CO2 concentration in the BSCs where Rubisco is located (Hatch, 1987). Pyruvate moves from the BSCs into the chloroplasts of the MCs where it is converted to PEP by pyruvate:phosphate dikinase (PPDK)

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