In Vivo Interactions between Photosynthesis, Mitorespiration, and Chlororespiration in Chlamydomonas reinhardtii

Author:

Cournac Laurent1,Latouche Gwendal2,Cerovic Zoran2,Redding Kevin3,Ravenel Jacques1,Peltier Gilles1

Affiliation:

1. Commissariat à l'Energie Atomique (CEA) Cadarache, Direction des Sciences du Vivant, Département d'Ecophysiologie Végétale et de Microbiologie, Laboratoire d'Ecophysiologie de la Photosynthèse, Unité Mixte de Recherche 163 Centre National de la Recherche Scientifique CEA, Univ-Méditerranée CEA 1000, F–13108 Saint-Paul-lez-Durance cedex, France (L.C., J.R., G.P.);

2. Laboratoire pour l'Utilisation du Rayonnement Electromagnétique-Centre National de la Recherche Scientifique, Bat 203, Boı̂te Postale 34, Centre Universitaire Paris-Sud, Equipe Photosynthèse et Télédétection, F–91898 Orsay, France (G.L., Z.C.); and

3. Department of Chemistry, 120 Lloyd Hall, 6th Avenue, University of Alabama, Tuscaloosa, Alabama 35487–0336 (K.R.)

Abstract

Abstract Interactions between photosynthesis, mitochondrial respiration (mitorespiration), and chlororespiration have been investigated in the green alga Chlamydomonas reinhardtiiusing flash illumination and a bare platinum electrode. Depending on the physiological status of algae, flash illumination was found to induce either a fast (t1/2 ≈ 300 ms) or slow (t1/2 ≈ 3 s) transient inhibition of oxygen uptake. Based on the effects of the mitorespiratory inhibitors myxothiazol and salicyl hydroxamic acid (SHAM), and of propyl gallate, an inhibitor of the chlororespiratory oxidase, we conclude that the fast transient is due to the flash-induced inhibition of chlororespiration and that the slow transient is due to the flash-induced inhibition of mitorespiration. By measuring blue-green fluorescence changes, related to the redox status of the pyridine nucleotide pool, and chlorophyll fluorescence, related to the redox status of plastoquinones (PQs) in C.  reinhardtii wild type and in a photosystem I-deficient mutant, we show that interactions between photosynthesis and chlororespiration are favored when PQ and pyridine nucleotide pools are reduced, whereas interactions between photosynthesis and mitorespiration are favored at more oxidized states. We conclude that the plastid oxidase, similar to the mitochondrial alternative oxidase, becomes significantly engaged when the PQ pool becomes highly reduced, and thereby prevents its over-reduction.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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