PEPc-mediated CO2 assimilation provides carbons to gluconeogenesis and
the TCA cycle in both dark-exposed and illuminated guard cells
Abstract
Evidence suggests that guard cells have higher rate of
phosphoenolpyruvate carboxylase (PEPc)-mediated dark CO2 assimilation
than mesophyll cells. However, it is unknown which metabolic pathways
are activated following dark CO2 assimilation in guard cells.
Furthermore, it remains unclear how the metabolic fluxes throughout the
tricarboxylic acid (TCA) cycle and associated pathways are regulated in
illuminated guard cells. Here we used 13C-HCO3 labelling of tobacco
guard cells harvested under continuous dark or during the dark-to-light
transition to elucidate principles of metabolic dynamics downstream of
CO2 assimilation. Most metabolic changes were similar between
dark-exposed and illuminated guard cells. However, illumination
increased the 13C-enrichment in sugars and metabolites associated to the
TCA cycle. Sucrose was labelled in the dark, but light exposure
increased the 13C-labelling into this metabolite. Fumarate was strongly
labelled under both dark and light conditions, while illumination
increased the 13C-enrichment in pyruvate, succinate and glutamate. Only
one 13C was incorporated into malate and citrate in either dark or light
conditions. Our results collectively suggest that the PEPc-mediated CO2
assimilation provides carbons for gluconeogenesis, the TCA cycle and
glutamate synthesis and that previously stored malate and citrate are
used to underpin the specific metabolic requirements of illuminated
guard cells.