Plant Physiol. Illumina
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (47)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bakrim, N.
Right arrow Articles by Chollet, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bakrim, N.
Right arrow Articles by Chollet, R.
Agricola
Right arrow Articles by Bakrim, N.
Right arrow Articles by Chollet, R.

PLANT PHYSIOLOGY , Vol 101, Issue 3 891-897, Copyright © 1993 by American Society of Plant Biologists


METABOLISM AND ENZYMOLOGY

Regulatory Phosphorylation of C4 Phosphoenolpyruvate Carboxylase (A Cardinal Event Influencing the Photosynthesis Rate in Sorghum and Maize)

N. Bakrim, J. L. Prioul, E. Deleens, J. P. Rocher, M. Arrio-Dupont, J. Vidal, P. Gadal and R. Chollet
Laboratoire de Physiologie Vegetale Moleculaire (N.B., M.A.-D., J.V., P.G.) and Laboratoire de Structure et Metabolisme des Plantes (J.-L.P., E.D., J.-P.R.), URA Centre National de la Recherche Scientifique D 1128, Universite de Paris-Sud, Centre d'Orsay, Batiment 430, 91405 Orsay Cedex, France

C4 leaf phosphoenolpyruvate carboxylase (PEPC; EC 4.1.1.31) is subject to a day/night regulatory phosphorylation cycle. By using the cytoplasmic protein synthesis inhibitor cycloheximide (CHX), we previously reported that the reversible in vivo light activation of the C4 PEPC protein-serine kinase requires protein synthesis. In the present leaf gas-exchange study, we have examined how and to what extent the CHX-induced inhibition of PEPC protein kinase activity/PEPC phosphorylation in the light influences C4 photosynthesis. Detached Sorghum vulgare and maize (Zea mays) leaves fed 10 [mu]M CHX showed a gradual but marked decrease in photosynthetic CO2 assimilation capacity. A series of control experiments designed to assess deleterious secondary effects of the inhibitor established that this reduction in C4 leaf CO2 assimilation was not due to (a) an increased stomatal resistance to CO2 diffusion, (b) a decrease in the activation state of other photoactivated C4 cycle enzymes, and (c) a perturbation of the Benson-Calvin C3 cycle, as evidenced by the absence of an inhibitory effect of CHX on leaf photosynthesis by a C3 grass (Triticum aestivum). It is notable that the CHX-induced decrease in CO2 assimilation by illuminated Sorghum leaves was highly correlated with a decrease in the apparent phosphorylation status of PEPC and a concomitant change in carbon isotope discrimination consistent with a shift from a C4 to a C3 mode of leaf CO2 fixation. These collective findings indicate that the light-dependent activation of the PEPC protein-serine kinase and the resulting phosphorylation of serine-8 or serine-15 in Sorghum or maize PEPC, respectively, are fundamental regulatory events that influence leaf C4 photosynthesis in vivo.


This article has been cited by other articles:


Home page
Mol. Cell. ProteomicsHome page
Z. Shen, P. Li, R.-J. Ni, M. Ritchie, C.-P. Yang, G.-F. Liu, W. Ma, G.-J. Liu, L. Ma, S.-J. Li, et al.
Label-free Quantitative Proteomics Analysis of Etiolated Maize Seedling Leaves during Greening
Mol. Cell. Proteomics, November 1, 2009; 8(11): 2443 - 2460.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
T. Furumoto, K. Izui, V. Quinn, R. T. Furbank, and S. von Caemmerer
Phosphorylation of Phosphoenolpyruvate Carboxylase Is Not Essential for High Photosynthetic Rates in the C4 Species Flaveria bidentis
Plant Physiology, August 1, 2007; 144(4): 1936 - 1945.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
M. Jeanneau, J. Vidal, A. Gousset-Dupont, B. Lebouteiller, M. Hodges, D. Gerentes, and P. Perez
Manipulating PEPC levels in plants
J. Exp. Bot., September 1, 2002; 53(376): 1837 - 1845.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
H. Saze, Y. Ueno, T. Hisabori, H. Hayashi, and K. Izui
Thioredoxin-Mediated Reductive Activation of a Protein Kinase for the Regulatory Phosphorylation of C4-form Phosphoenolpyruvate Carboxylase from Maize
Plant Cell Physiol., December 1, 2001; 42(12): 1295 - 1302.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
E.H. Murchie, S. Ferrario-Mery, M-H. Valadier, and C.H. Foyer
Short-term nitrogen-induced modulation of phosphoenolpyruvate carboxylase in tobacco and maize leaves
J. Exp. Bot., August 1, 2000; 51(349): 1349 - 1356.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
K. Parvathi, A.S. Bhagwat, Y. Ueno, K. Izui, and A.S. Raghavendra
Illumination Increases the Affinity of Phosphoenolpyruvate Carboxylase to Bicarbonate in Leaves of a C4 Plant, Amaranthus hypochondriacus
Plant Cell Physiol., August 1, 2000; 41(8): 905 - 910.
[Abstract] [Full Text] [PDF]


Home page
Crop Sci.Home page
H. Brück, W.A. Payne, and B. Sattelmacher
Effects of Phosphorus and Water Supply on Yield, Transpirational Water-Use Efficiency, and Carbon Isotope Discrimination of Pearl Millet
Crop Sci., January 1, 2000; 40(1): 120 - 125.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
C. H. Foyer, M.-H. Valadier, A. Migge, and T. W. Becker
Drought-Induced Effects on Nitrate Reductase Activity and mRNA and on the Coordination of Nitrogen and Carbon Metabolism in Maize Leaves
Plant Physiology, May 1, 1998; 117(1): 283 - 292.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1993 by the American Society of Plant Biologists