Metabolic modelling identifies mitochondrial Pi uptake and pyruvate efflux as key aspects of daytime metabolism and proton homeostasis in crassulacean acid metabolism leaves
- PMID: 39113419
- DOI: 10.1111/nph.20032
Metabolic modelling identifies mitochondrial Pi uptake and pyruvate efflux as key aspects of daytime metabolism and proton homeostasis in crassulacean acid metabolism leaves
Abstract
Crassulacean acid metabolism (CAM) leaves are characterized by nocturnal acidification and diurnal deacidification processes related with the timed actions of phosphoenolpyruvate carboxylase and Rubisco, respectively. How CAM leaves manage cytosolic proton homeostasis, particularly when facing massive diurnal proton effluxes from the vacuole, remains unclear. A 12-phase flux balance analysis (FBA) model was constructed for a mature malic enzyme-type CAM mesophyll cell in order to predict diel kinetics of intracellular proton fluxes. The charge- and proton-balanced FBA model identified the mitochondrial phosphate carrier (PiC, Pi/H+ symport), which provides Pi to the matrix to sustain ATP biosynthesis, as a major consumer of cytosolic protons during daytime (> 50%). The delivery of Pi to the mitochondrion, co-transported with protons, is required for oxidative phosphorylation and allows sufficient ATP to be synthesized to meet the high energy demand during CAM Phase III. Additionally, the model predicts that mitochondrial pyruvate originating from decarboxylation of malate is exclusively exported to the cytosol, probably via a pyruvate channel mechanism, to fuel gluconeogenesis. In this biochemical cycle, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) acts as another important cytosolic proton consumer. Overall, our findings emphasize the importance of mitochondria in CAM and uncover a hitherto unappreciated role in metabolic proton homeostasis.
Keywords: CAM mitochondria; crassulacean acid metabolism (CAM); diurnal deacidification; flux balance analysis modelling; malic enzyme‐type CAM leaf; metabolic proton homeostasis; mitochondrial phosphate carrier (PiC); vacuolar proton efflux.
© 2024 The Author(s). New Phytologist © 2024 New Phytologist Foundation.
Similar articles
-
How to resolve the enigma of diurnal malate remobilisation from the vacuole in plants with crassulacean acid metabolism?New Phytol. 2021 Mar;229(6):3116-3124. doi: 10.1111/nph.17070. Epub 2020 Dec 30. New Phytol. 2021. PMID: 33159327
-
Feasibility of a mitochondrial pyruvate malate shuttle in pancreatic islets. Further implication of cytosolic NADPH in insulin secretion.J Biol Chem. 1995 Aug 25;270(34):20051-8. J Biol Chem. 1995. PMID: 7650022
-
Plastidic metabolite transporters and their physiological functions in the inducible crassulacean acid metabolism plant Mesembryanthemum crystallinum.Plant J. 2000 Nov;24(3):285-96. doi: 10.1046/j.1365-313x.2000.00876.x. Plant J. 2000. PMID: 11069702
-
CO(2)-concentrating: consequences in crassulacean acid metabolism.J Exp Bot. 2002 Nov;53(378):2131-42. doi: 10.1093/jxb/erf081. J Exp Bot. 2002. PMID: 12379779 Review.
-
Prospects and perspectives: inferring physiological and regulatory targets for CAM from molecular and modelling approaches.Ann Bot. 2023 Nov 25;132(4):583-596. doi: 10.1093/aob/mcad142. Ann Bot. 2023. PMID: 37742290 Free PMC article. Review.
Cited by
-
Synthetic crassulacean acid metabolism (SynCAM) for improving water-use efficiency in plants.Philos Trans R Soc Lond B Biol Sci. 2025 May 29;380(1927):20240249. doi: 10.1098/rstb.2024.0249. Epub 2025 May 29. Philos Trans R Soc Lond B Biol Sci. 2025. PMID: 40439297 Review.
References
-
- Abraham PE, Hurtado Castano N, Cowan‐Turner D, Barnes J, Poudel S, Hettich R, Flütsch S, Santelia D, Borland AM. 2020. Peeling back the layers of crassulacean acid metabolism: functional differentiation between Kalanchoë fedtschenkoi epidermis and mesophyll proteomes. The Plant Journal 103: 869–888.
-
- Abraham PE, Yin H, Borland AM, Weighill D, Lim SD, De Paoli HC, Engle N, Jones PC, Agh R, Weston DJ et al. 2016. Transcript, protein and metabolite temporal dynamics in the CAM plant Agave. Nature Plants 2: 1–10.
-
- Bartholomew DM, Rees DJG, Rambaut A, Smith JAC. 1996. Isolation and sequence analysis of a cDNA encoding the c subunit of a vacuolar‐type H+‐ATPase from the CAM plant Kalanchoë daigremontiana. Plant Molecular Biology 31: 435–442.
-
- Borland AM, Barrera Zambrano VA, Ceusters J, Shorrock K. 2011. The photosynthetic plasticity of crassulacean acid metabolism: an evolutionary innovation for sustainable productivity in a changing world. New Phytologist 191: 619–633.
-
- Borland AM, Griffiths H, Hartwell J, Smith JAC. 2009. Exploiting the potential of plants with crassulacean acid metabolism for bioenergy production on marginal lands. Journal of Experimental Botany 60: 2879–2896.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous