Novel guard cell sink characteristics revealed by a multi-species/cell-types meta-analysis of ¹³C-labelling experiments

The tricarboxylic acid (TCA) cycle is an important metabolic pathway to underpin stomatal movements, given that respiration is thought to be the main energy source for guard cell (GC) metabolism. However, it is still unclear how the metabolic fluxes throughout the TCA cycle and associated pathways are regulated in GCs. Here we used a C-13-positional isotopomer approach and performed a multi-species/cell-types analysis based on previous( 13)C-labelling studies carried out using Arabidopsis rosettes, maize leaves, Arabidopsis source and sink leaves, and isolated GCs from Arabidopsis and tobacco. We aimed to compare flux modes through the TCA cycle and associated pathways in GCs and leaves, which are mostly composed by mesophyll cells (MCs). Mesophyll cells showed high C-13-enrichment into alanine and aspartate following provision of (CO2)-C-13, whilst GCs and sink MCs showed high( 13)C-incorporation into glutamate/glutamine following provision of C-13-sucrose. Only GCs showed high C-13-enrichment in the carbon 1 atom of glutamine, which is derived from phosphoenolpyruvate carboxylase (PEPc)-mediated CO2 assimilation. The PEPc-mediated C-13-incorporation into malate was similar between GCs and MCs, but GCs had higher C-13-enrichment and accumulation of fumarate than MCs. The metabolic fluxes throughout the TCA cycle of illuminated GCs resemble those of sink MCs, but with different contribution from PEPc, glycolysis and the TCA cycle to glutamate/glutamine synthesis. We further demonstrate that transamination reactions catalysed by alanine and aspartate amino transferases may support non-cyclic TCA flux modes in illuminated MCs.