Analysis of companion cell and phloem metabolism using a transcriptome-guided model of Arabidopsis metabolism

Author:

Hunt Hilary1,Brueggen Nico2,Galle Alexander3,Vanderauwera Sandy3,Frohberg Claus3,Fernie Alisdair R4,Sonnewald Uwe2,Sweetlove Lee J1

Affiliation:

1. Department of Plant Sciences, University of Oxford , South Parks Rd, Oxford OX1 3RB , UK

2. Department of Biology, Division of Biochemistry, Friedrich–Alexander University Erlangen–Nürnberg , Staudtstrasse 5, Erlangen 91ß58 , Germany

3. BASF Belgium Coordination Center CommV, Innovation Center Gent , Technologiepark-Zwijnaarde 101, Gent 9052 , Belgium

4. Max Planck Institute of Molecular Plant Physiology , Am Mühlenberg 1, Potsdam 14476 , Germany

Abstract

AbstractCompanion cells and sieve elements play an essential role in vascular plants, and yet the details of the metabolism that underpins their function remain largely unknown. Here, we construct a tissue-scale flux balance analysis (FBA) model to describe the metabolism of phloem loading in a mature Arabidopsis (Arabidopsis thaliana) leaf. We explore the potential metabolic interactions between mesophyll cells, companion cells, and sieve elements based on the current understanding of the physiology of phloem tissue and through the use of cell type–specific transcriptome data as a weighting in our model. We find that companion cell chloroplasts likely play a very different role to mesophyll chloroplasts. Our model suggests that, rather than carbon capture, the most crucial function of companion cell chloroplasts is to provide photosynthetically generated ATP to the cytosol. Additionally, our model predicts that the metabolites imported into the companion cell are not necessarily the same metabolites that are exported in phloem sap; phloem loading is more efficient if certain amino acids are synthesized in the phloem tissue. Surprisingly, in our model predictions, the proton-pumping pyrophosphatase (H+-PPiase) is a more efficient contributor to the energization of the companion cell plasma membrane than the H+-ATPase.

Funder

BASF

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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