| Literature DB >> 24894045 |
Tabea Mettler1, Timo Mühlhaus1, Dorothea Hemme1, Mark-Aurel Schöttler1, Jens Rupprecht1, Adam Idoine1, Daniel Veyel1, Sunil Kumar Pal1, Liliya Yaneva-Roder1, Flavia Vischi Winck2, Frederik Sommer1, Daniel Vosloh1, Bettina Seiwert1, Alexander Erban1, Asdrubal Burgos1, Samuel Arvidsson2, Stephanie Schönfelder1, Anne Arnold1, Manuela Günther1, Ursula Krause1, Marc Lohse1, Joachim Kopka1, Zoran Nikoloski1, Bernd Mueller-Roeber2, Lothar Willmitzer1, Ralph Bock1, Michael Schroda1, Mark Stitt3.
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 (R2 = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.Entities:
Year: 2014 PMID: 24894045 PMCID: PMC4114937 DOI: 10.1105/tpc.114.124537
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277