Cross-compartment metabolic coupling enables flexible photoprotective mechanisms in the diatom Phaeodactylum tricornutum

© 2019 J. Craig Venter Institute New Phytologist © 2019 New Phytologist Trust.

Bibliographische Detailangaben
Veröffentlicht in:The New phytologist. - 1984. - 222(2019), 3 vom: 21. Mai, Seite 1364-1379
1. Verfasser: Broddrick, Jared T (VerfasserIn)
Weitere Verfasser: Du, Niu, Smith, Sarah R, Tsuji, Yoshinori, Jallet, Denis, Ware, Maxwell A, Peers, Graham, Matsuda, Yusuke, Dupont, Chris L, Mitchell, B Greg, Palsson, Bernhard O, Allen, Andrew E
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2019
Zugriff auf das übergeordnete Werk:The New phytologist
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Phaeodactylum tricornutum analysis diatom energy metabolism flux balance genome-scale modeling photorespiration mehr... Pyruvic Acid 8558G7RUTR Alcohol Oxidoreductases EC 1.1.- glycollate oxidase EC 1.1.3.15
Beschreibung
Zusammenfassung:© 2019 J. Craig Venter Institute New Phytologist © 2019 New Phytologist Trust.
Photoacclimation consists of short- and long-term strategies used by photosynthetic organisms to adapt to dynamic light environments. Observable photophysiology changes resulting from these strategies have been used in coarse-grained models to predict light-dependent growth and photosynthetic rates. However, the contribution of the broader metabolic network, relevant to species-specific strategies and fitness, is not accounted for in these simple models. We incorporated photophysiology experimental data with genome-scale modeling to characterize organism-level, light-dependent metabolic changes in the model diatom Phaeodactylum tricornutum. Oxygen evolution and photon absorption rates were combined with condition-specific biomass compositions to predict metabolic pathway usage for cells acclimated to four different light intensities. Photorespiration, an ornithine-glutamine shunt, and branched-chain amino acid metabolism were hypothesized as the primary intercompartment reductant shuttles for mediating excess light energy dissipation. Additionally, simulations suggested that carbon shunted through photorespiration is recycled back to the chloroplast as pyruvate, a mechanism distinct from known strategies in photosynthetic organisms. Our results suggest a flexible metabolic network in P. tricornutum that tunes intercompartment metabolism to optimize energy transport between the organelles, consuming excess energy as needed. Characterization of these intercompartment reductant shuttles broadens our understanding of energy partitioning strategies in this clade of ecologically important primary producers
Beschreibung:Date Completed 27.02.2020
Date Revised 30.09.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1469-8137
DOI:10.1111/nph.15685