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


     


First published online August 24, 2007; 10.1104/pp.107.103713

Plant Physiology 145:513-526 (2007)
© 2007 American Society of Plant Biologists

OPEN ACCESS ARTICLE
This Article
Free via Open Access: OA
Right arrow OA Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow Supplemental Data
Right arrowOA All Versions of this Article:
145/2/513    most recent
pp.107.103713v1
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 Related articles in Plant Physiol.
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 (19)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhu, X.-G.
Right arrow Articles by Long, S. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhu, X.-G.
Right arrow Articles by Long, S. P.
Agricola
Right arrow Articles by Zhu, X.-G.
Right arrow Articles by Long, S. P.
BIOENERGETICS AND PHOTOSYNTHESIS

Optimizing the Distribution of Resources between Enzymes of Carbon Metabolism Can Dramatically Increase Photosynthetic Rate: A Numerical Simulation Using an Evolutionary Algorithm1,[W],[OA]

Xin-Guang Zhu, Eric de Sturler and Stephen P. Long*

Department of Plant Biology and Crop Sciences (X.-G.Z., S.P.L.) and Institute for Genomic Biology (S.P.L.), University of Illinois at Urbana-Champaign, Urbana, Illinois 61801; Department of Mathematics, Virginia Tech, Blacksburg, Virginia 24601–0123 (E.d.S.); and National Center for Supercomputing Applications, Urbana, Illinois 61801 (X.-G.Z., S.P.L.)

The distribution of resources between enzymes of photosynthetic carbon metabolism might be assumed to have been optimized by natural selection. However, natural selection for survival and fecundity does not necessarily select for maximal photosynthetic productivity. Further, the concentration of a key substrate, atmospheric CO2, has changed more over the past 100 years than the past 25 million years, with the likelihood that natural selection has had inadequate time to reoptimize resource partitioning for this change. Could photosynthetic rate be increased by altered partitioning of resources among the enzymes of carbon metabolism? This question is addressed using an "evolutionary" algorithm to progressively search for multiple alterations in partitioning that increase photosynthetic rate. To do this, we extended existing metabolic models of C3 photosynthesis by including the photorespiratory pathway (PCOP) and metabolism to starch and sucrose to develop a complete dynamic model of photosynthetic carbon metabolism. The model consists of linked differential equations, each representing the change of concentration of one metabolite. Initial concentrations of metabolites and maximal activities of enzymes were extracted from the literature. The dynamics of CO2 fixation and metabolite concentrations were realistically simulated by numerical integration, such that the model could mimic well-established physiological phenomena. For example, a realistic steady-state rate of CO2 uptake was attained and then reattained after perturbing O2 concentration. Using an evolutionary algorithm, partitioning of a fixed total amount of protein-nitrogen between enzymes was allowed to vary. The individual with the higher light-saturated photosynthetic rate was selected and used to seed the next generation. After 1,500 generations, photosynthesis was increased substantially. This suggests that the "typical" partitioning in C3 leaves might be suboptimal for maximizing the light-saturated rate of photosynthesis. An overinvestment in PCOP enzymes and underinvestment in Rubisco, sedoheptulose-1,7-bisphosphatase, and fructose-1,6-bisphosphate aldolase were indicated. Increase in sink capacity, such as increase in ADP-glucose pyrophosphorylase, was also indicated to lead to increased CO2 uptake rate. These results suggest that manipulation of partitioning could greatly increase carbon gain without any increase in the total protein-nitrogen investment in the apparatus for photosynthetic carbon metabolism.


1 This work was co-supported by the National Center for Supercomputing Applications at the University of Illinois and the U.S. National Science Foundation (grant no. IBN 04–17126).

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Stephen P. Long (stevel{at}life.uiuc.edu).

[W] The online version of this article contains Web-only data.

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.103713

* Corresponding author; e-mail stevel{at}life.uiuc.edu.

Received June 11, 2007; accepted July 22, 2007; published August 24, 2007.


Related articles in Plant Physiol.:

On the Inside
Peter V. Minorsky
Plant Physiol. 2007 145: 291-292. [Full Text]  



This article has been cited by other articles:


Home page
J Exp BotHome page
A. D. B. Leakey, E. A. Ainsworth, C. J. Bernacchi, A. Rogers, S. P. Long, and D. R. Ort
Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE
J. Exp. Bot., July 1, 2009; 60(10): 2859 - 2876.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
S. M. Whitney, H. J. Kane, R. L. Houtz, and R. E. Sharwood
Rubisco Oligomers Composed of Linked Small and Large Subunits Assemble in Tobacco Plastids and Have Higher Affinities for CO2 and O2
Plant Physiology, April 1, 2009; 149(4): 1887 - 1895.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
W. Yamori, K. Noguchi, K. Hikosaka, and I. Terashima
Cold-Tolerant Crop Species Have Greater Temperature Homeostasis of Leaf Respiration and Photosynthesis Than Cold-Sensitive Species
Plant Cell Physiol., February 1, 2009; 50(2): 203 - 215.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
E. A. Ainsworth, A. Rogers, and A. D.B. Leakey
Targets for Crop Biotechnology in a Future High-CO2 and High-O3 World
Plant Physiology, May 1, 2008; 147(1): 13 - 19.
[Full Text] [PDF]


Home page
Plant Physiol.Home page
K. Century, T. L. Reuber, and O. J. Ratcliffe
Regulating the Regulators: The Future Prospects for Transcription-Factor-Based Agricultural Biotechnology Products
Plant Physiology, May 1, 2008; 147(1): 20 - 29.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2007 by the American Society of Plant Biologists