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


     


Plant Physiology 65:331-335 (1980)
© 1980 American Society of Plant Biologists

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 (81)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holaday, A. S.
Right arrow Articles by Bowes, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holaday, A. S.
Right arrow Articles by Bowes, G.
Agricola
Right arrow Articles by Holaday, A. S.
Right arrow Articles by Bowes, G.
Articles

C4 Acid Metabolism and Dark CO2 Fixation in a Submersed Aquatic Macrophyte (Hydrilla verticillata) 1

A. Scott Holaday2 and George Bowes3

Department of Botany, University of Florida, Gainesville, Florida 32611

The CO2 compensation point of the submersed aquatic macrophyte Hydrilla verticillata varied from high (above 50 microliters per liter) to low (10 to 25 microliters per liter) values, depending on the growth conditions. Plants from the lake in winter or after incubation in an 11 C/9-hour photoperiod had high values, whereas summer plants or those incubated in a 27 C/14-hour photoperiod had low values. The plants with low CO2 compensation points exhibited dark 14CO2 fixation rates that were up to 30% of the light fixation rates. This fixation reduced respiratory CO2 loss, but did not result in a net uptake of CO2 at night. The low compensation point plants also showed diurnal fluctuations in titratable acid, such as occur in Crassulacean acid metabolism plants. However, dark fixation and diurnal acid fluctuations were negligible in Hydrilla plants with high CO2 compensation points.

Exposure of the low compensation point plants to 20 micromolar 14CO2 resulted in 60% of the 14C being incorporated into malate and aspartate, with only 16% in sugar phosphates. At a high CO2 level, the C4 acid label was decreased. A pulse-chase study indicated that the 14C in malate, but not aspartate, decreased after a long (270-second) chase period; thus, the C4 acid turnover was much slower than in C4 plants.

Phosphoenolpyruvate carboxylase activity was high (330 micromoles per milligram chlorophyll per hour), as compared to ribulose bisphosphate carboxylase (20 to 25), in the plants with low compensation points. These plants also had a pyruvate, Pi dikinase activity in the leaves of 41 micromoles per milligram chlorophyll per hour, which suggests they are not C3 plants. NAD- and NADP+-malate dehydrogenase activities were 6136 and 24.5 micromoles per milligram chlorophyll per hour, respectively. Of the three decarboxylating enzymes assayed, the activities of NAD- and NADP+-malic enzyme were 104.2 and 23.7 micromoles per milligram chlorophyll per hour, while phosphoenolpyruvate carboxykinase was only 0.2.

Low compensation point Hydrilla plants fix some CO2 into C4 acids, which can be decarboxylated for later refixation, presumably into the Calvin cycle. Refixation would be advantageous in summer lake environments where the CO2 levels are high at night but low during the day. Hydrilla does not fit any of the present photosynthetic categories, and may have to be placed into a new group, together with other submersed aquatic macrophytes that have environmentally variable CO2 compensation points.


2 Present address: Biochemistry Department, University of Georgia, Athens, Georgia 30602.

3 To whom requests for reprints should be addressed.

1 This research was supported in part by the Science and Education Administration of the United States Department of Agriculture under Grant 5901-0410-8-0082-0 from the Competitive Research Grants Office, and by the Florida Department of Natural Resources, Grant 249-K17. Florida Agricultural Experiment Station Journal Series No. 1804.




This article has been cited by other articles:


Home page
ANN BOT (LOND)Home page
L. MOMMER and E. J. W. VISSER
Underwater Photosynthesis in Flooded Terrestrial Plants: A Matter of Leaf Plasticity
Ann. Bot., September 1, 2005; 96(4): 581 - 589.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
P. WESTHOFF and U. GOWIK
Evolution of C4 Phosphoenolpyruvate Carboxylase. Genes and Proteins: a Case Study with the Genus Flaveria
Ann. Bot., January 1, 2004; 93(1): 13 - 23.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
R. E. Hausler, H.-J. Hirsch, F. Kreuzaler, and C. Peterhansel
Overexpression of C4-cycle enzymes in transgenic C3 plants: a biotechnological approach to improve C3-photosynthesis
J. Exp. Bot., April 1, 2002; 53(369): 591 - 607.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1980 by the American Society of Plant Biologists