Metabolic modelling identifies mitochondrial Pi uptake and pyruvate efflux as key aspects of daytime metabolism and proton homeostasis in crassulacean acid metabolism leaves

© 2024 The Author(s). New Phytologist © 2024 New Phytologist Foundation.

Détails bibliographiques
Publié dans:The New phytologist. - 1979. - 244(2024), 1 vom: 07. Okt., Seite 159-175
Auteur principal: Daems, Stijn (Auteur)
Autres auteurs: Shameer, Sanu, Ceusters, Nathalie, Sweetlove, Lee, Ceusters, Johan
Format: Article en ligne
Langue:English
Publié: 2024
Accès à la collection:The New phytologist
Sujets:Journal Article 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 Protons plus... Pyruvic Acid 8558G7RUTR Phosphates Malates malic acid 817L1N4CKP Adenosine Triphosphate 8L70Q75FXE
Description
Résumé:© 2024 The Author(s). New Phytologist © 2024 New Phytologist Foundation.
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
Description:Date Completed 16.09.2024
Date Revised 16.09.2024
published: Print-Electronic
Citation Status MEDLINE
ISSN:1469-8137
DOI:10.1111/nph.20032