SummaryC 4 photosynthesis involves alterations to leaf development, cell biology and biochemistry. Different lineages of C 4 plants use varying mechanisms to generate the C 4 pathway. Although the biochemistry of C 4 photosynthesis was described around 20 years ago, the phylogenetic distance between Arabidopsis and the traditional C 4 models has not facilitated the transfer of knowledge from Arabidopsis research to understanding C 4 systems. We show that Cleome, a genus closely related to Arabidopsis, contains species spanning a developmental progression from C 3 to C 4 photosynthesis. The majority of species we assessed are C 3 plants but have increased venation in leaves. Three C 3 species have both increased venation and enlarged bundle sheath cells, and there is also a tendency to accumulate proteins and transcripts needed for C 4 photosynthesis. Cleome gynandra shows all the characteristics needed for efficient C 4 photosynthesis, including alterations to leaf biochemistry, cell biology and development, and belongs to the NAD-dependent malic enzyme subtype. Combined with its phylogenetic proximity to Arabidopsis, the developmental progression from C 3 to C 4 photosynthesis within the genus provides a potentially excellent new model to increase our understanding of C 4 photosynthesis, and provide insights into its evolution.

C₄ photosynthesis allows increased photosynthetic efficiency because carbon dioxide (CO₂) is concentrated around the key enzyme RuBisCO. Leaves of C₄ plants exhibit modified biochemistry, cell biology, and leaf development, but despite this complexity, C₄ photosynthesis has evolved independently in at least 45 lineages of plants. We found that two independent lineages of C₄ plant, whose last common ancestor predates the divergence of monocotyledons and dicotyledons about 180 million years ago, show conserved mechanisms controlling the expression of genes important for release of CO(2) around RuBisCO in bundle sheath (BS) cells. Orthologous genes from monocotyledonous and dicotyledonous C₃ species also contained conserved regulatory elements that conferred BS specificity when placed into C₄ species. We conclude that these conserved functional genetic elements likely facilitated the repeated evolution of C₄ photosynthesis.

Our most productive crops and native vegetation use a modified version of photosynthesis known as the C(4) pathway. Leaves of C(4) crops have increased nitrogen and water use efficiencies compared with C(3) species. Although the modifications to leaves of C(4) plants are complex, their faster growth led to the proposal that C(4) photosynthesis should be installed in C(3) crops in order to increase yield potential. Typically, a limited set of proteins become restricted to mesophyll or bundle sheath cells, and this allows CO(2) to be concentrated around the primary carboxylase RuBisCO. The role that these proteins play in C(3) species prior to their recruitment into the C(4) pathway is addressed here. Understanding the role of these proteins in C(3) plants is likely to be of use in predicting how the metabolism of a C(3) leaf will alter as components of the C(4) pathway are introduced as part of efforts to install characteristics of C(4) photosynthesis in leaves of C(3) crops.

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SUMMARYCells associated with veins of petioles of C 3 tobacco possess high activities of the decarboxylase enzymes required in C 4 photosynthesis. It is not clear whether this is the case in other C 3 species, nor whether these enzymes provide precursors for specific biosynthetic pathways. Here, we investigate the activity of C 4 acid decarboxylases in the mid-vein of Arabidopsis, identify regulatory regions sufficient for this activity, and determine the impact of removing individual isoforms of each protein on mid-vein metabolite profiles. This showed that radiolabelled malate and bicarbonate fed to the xylem stream were incorporated into soluble and insoluble material in the mid-vein of Arabidopsis leaves. Compared with the leaf lamina, mid-veins possessed high activities of NADP-dependent malic enzyme (NADP-ME), NAD-dependent malic enzyme (NAD-ME) and phosphoenolpyruvate carboxykinase (PEPCK). Transcripts derived from both NAD-ME, one PCK and two of the four NADP-ME genes were detectable in these veinal cells. The promoters of each decarboxylase gene were sufficient for expression in mid-veins. Analysis of insertional mutants revealed that cytosolic NADP-ME2 is responsible for 80% of NADP-ME activity in mid-veins. Removing individual decarboxylases affected the abundance of amino acids derived from pyruvate and phosphoenolpyruvate. Reducing cytosolic NADP-ME activity preferentially affected the sugar content, whereas abolishing NAD-ME affected both the amino acid and the glucosamine content of mid-veins.