AUTHOR=Lim Sung Don , Lee Sojeong , Choi Won-Gyu , Yim Won Cheol , Cushman John C. 

TITLE=Laying the Foundation for Crassulacean Acid Metabolism (CAM) Biodesign: Expression of the C4 Metabolism Cycle Genes of CAM in Arabidopsis

JOURNAL=Frontiers in Plant Science

VOLUME=10

YEAR=2019

URL=https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2019.00101

DOI=10.3389/fpls.2019.00101

ISSN=1664-462X

ABSTRACT=<p>Crassulacean acid metabolism (CAM) is a specialized mode of photosynthesis that exploits a temporal CO<sub>2</sub> pump with nocturnal CO<sub>2</sub> uptake and concentration to reduce photorespiration, improve water-use efficiency (WUE), and optimize the adaptability of plants to hotter and drier climates. Introducing the CAM photosynthetic machinery into C<sub>3</sub> (or C<sub>4</sub>) photosynthesis plants (CAM Biodesign) represents a potentially breakthrough strategy for improving WUE while maintaining high productivity. To optimize the success of CAM Biodesign approaches, the functional analysis of individual C<sub>4</sub> metabolism cycle genes is necessary to identify the essential genes for robust CAM pathway introduction. Here, we isolated and analyzed the subcellular localizations of 13 enzymes and regulatory proteins of the C<sub>4</sub> metabolism cycle of CAM from the common ice plant in stably transformed <italic>Arabidopsis thaliana</italic>. Six components of the carboxylation module were analyzed including beta-carbonic anhydrase (<italic>McBCA2</italic>), phosphoenolpyruvate carboxylase (<italic>McPEPC1</italic>), phosphoenolpyruvate carboxylase kinase (<italic>McPPCK1</italic>), NAD-dependent malate dehydrogenase (<italic>McNAD-MDH1</italic>, <italic>McNAD-MDH2</italic>), and NADP-dependent malate dehydrogenase (<italic>McNADP-MDH1</italic>). In addition, seven components of the decarboxylation module were analyzed including NAD-dependent malic enzyme (<italic>McNAD-ME1</italic>, <italic>McNAD-ME2</italic>), NADP-dependent malic enzyme (<italic>McNADP-ME1</italic>, <italic>NADP-ME2</italic>), pyruvate, orthophosphate dikinase (<italic>McPPDK</italic>), pyruvate, orthophosphate dikinase-regulatory protein (<italic>McPPDK-RP</italic>), and phosphoenolpyruvate carboxykinase (<italic>McPEPCK</italic>). Ectopic overexpression of most C<sub>4</sub>-metabolism cycle components resulted in increased rosette diameter, leaf area, and leaf fresh weight of <italic>A. thaliana</italic> except for <italic>McNADP-MDH1</italic>, <italic>McPPDK-RP</italic>, and <italic>McPEPCK.</italic> Overexpression of most carboxylation module components resulted in increased stomatal conductance and dawn/dusk titratable acidity (TA) as an indirect measure of organic acid (mainly malate) accumulation in <italic>A. thaliana</italic>. In contrast, overexpression of the decarboxylating malic enzymes reduced stomatal conductance and TA. This comprehensive study provides fundamental insights into the relative functional contributions of each of the individual components of the core C<sub>4</sub>-metabolism cycle of CAM and represents a critical first step in laying the foundation for CAM Biodesign.</p>