Systems Analysis of the Response of Photosynthesis, Metabolism, and Growth to an Increase in Irradiance in the Photosynthetic Model Organism Chlamydomonas reinhardtii

Author:

Mettler Tabea1,Mühlhaus Timo1,Hemme Dorothea1,Schöttler Mark-Aurel1,Rupprecht Jens1,Idoine Adam1,Veyel Daniel1,Pal Sunil Kumar1,Yaneva-Roder Liliya1,Winck Flavia Vischi12,Sommer Frederik1,Vosloh Daniel1,Seiwert Bettina1,Erban Alexander1,Burgos Asdrubal1,Arvidsson Samuel12,Schönfelder Stephanie1,Arnold Anne1,Günther Manuela1,Krause Ursula1,Lohse Marc1,Kopka Joachim1,Nikoloski Zoran1,Mueller-Roeber Bernd12,Willmitzer Lothar1,Bock Ralph1,Schroda Michael1,Stitt Mark1

Affiliation:

1. Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam-Golm, Germany

2. Institute of Biochemistry and Biology, University of Potsdam, 14476 Potsdam-Golm, Germany

Abstract

Abstract We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R  2 = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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