Abstract

In subfamily Suaedoideae, four independent gains of C4 photosynthesis are proposed, which includes two parallel origins of Kranz anatomy (sections Salsina and Schoberia) and two independent origins of single-cell C4 anatomy (Bienertia and Suaeda aralocaspica). Additional phylogenetic support for this hypothesis was generated from sequence data of the C-terminal portion of the phosphoenolpyruvate carboxylase (PEPC) gene used in C4 photosynthesis (ppc-1) in combination with previous sequence data. ppc-1 sequence was generated for 20 species in Suaedoideae and two outgroup Salsola species that included all types of C4 anatomies as well as two types of C3 anatomies. A branch-site test for positively selected codons was performed using the software package PAML. From labelling of the four branches where C4 is hypothesized to have developed (foreground branches), residue 733 (maize numbering) was identified to be under positive selection with a posterior probability >0.99 and residue 868 at the >0.95 interval using Bayes empirical Bayes (BEB). When labelling all the branches within C4 clades, the branch-site test identified 13 codons to be under selection with a posterior probability >0.95 by BEB; this is discussed considering current information on functional residues. The signature C4 substitution of an alanine for a serine at position 780 in the C-terminal end (which is considered a major determinant of affinity for PEP) was only found in four of the C4 species sampled, while eight of the C4 species and all the C3 species have an alanine residue; indicating that this substitution is not a requirement for C4 function.

Highlights

  • Phosphoenolpyruvate carboxylase (PEPC) (EC 4.1.1.31) plays an important biochemical role in higher plants by converting bicarbonate (HCO3–) and phosphoenolpyruvate (PEP), in the presence of Mg2+ or Mn2+, into the four-carbon acid oxaloacetate (OAA) and Pi (O’Leary, 1982; Chollet et al, 1996; Izui et al, 2004)

  • Additional phylogenetic support for this hypothesis was generated from sequence data of the C-terminal portion of the phosphoenolpyruvate carboxylase (PEPC) gene used in C4 photosynthesis in combination with previous sequence data. ppc-1 sequence was generated for 20 species in Suaedoideae and two outgroup Salsola species that included all types of C4 anatomies as well as two types of C3 anatomies

  • All plant genomes encode several paralogues of PEPC, with only one orthologue being used in Abbreviations: dN, non-synonmous substitution rate; dS, synonymous substitution rate; G6P, glucose 6-phosphate; LRT, likelihood ratio test; Maximum likelihood (ML), maximum likelihood; OAA, oxaloacetate; PEP, phosphoenolpyruvate; PEPC, phosphoenolpyruvate carboxylase; ω, the non-synonymous/synonymous substitution rate ratio

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Summary

Introduction

Phosphoenolpyruvate carboxylase (PEPC) (EC 4.1.1.31) plays an important biochemical role in higher plants by converting bicarbonate (HCO3–) and phosphoenolpyruvate (PEP), in the presence of Mg2+ or Mn2+, into the four-carbon acid oxaloacetate (OAA) and Pi (O’Leary, 1982; Chollet et al, 1996; Izui et al, 2004). Plants that have high levels of PEPC protein in their leaves to generate a pool of aspartate or malate as intermediate products of photosynthesis are known as C4 or CAM (Crassulacean acid metabolism) species, as opposed to C3 species that use PEPC primarily in an anaplerotic role. All plant genomes encode several paralogues of PEPC, with only one orthologue being used in Abbreviations: dN, non-synonmous substitution rate; dS, synonymous substitution rate; G6P, glucose 6-phosphate; LRT, likelihood ratio test; ML, maximum likelihood; OAA, oxaloacetate; PEP, phosphoenolpyruvate; PEPC, phosphoenolpyruvate carboxylase; ω, the non-synonymous/synonymous substitution rate ratio. The exact amino acid residues that are responsible for the various observed kinetic difference is still being resolved in order to explain further how PEPC kinetics impact the flux of CO2 assimilation through the C4 pathway under a wide range of changing conditions

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