Plant Physiol. Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
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 (17)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Falk, K. L.
Right arrow Articles by Oliver, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Falk, K. L.
Right arrow Articles by Oliver, D. J.
Agricola
Right arrow Articles by Falk, K. L.
Right arrow Articles by Oliver, D. J.

Metabolic Bypass of the Tricarboxylic Acid Cycle during Lipid Mobilization in Germinating Oilseeds1
Regulation of NAD+-Dependent Isocitrate Dehydrogenase Versus Fumarase

Kimberly L. Falk2, Robert H. Behal, Chengbin Xiang, and David J. Oliver*

Department of Microbiology, Molecular Biology and Biochemistry, University of Idaho, Moscow, Idaho 83844 (K.L.F.); and Department of Botany, Iowa State University, Ames, Iowa 50010 (R.H.B., C.X., D.J.O.)

Biosynthesis of sucrose from triacylglycerol requires the bypass of the CO2-evolving reactions of the tricarboxylic acid (TCA) cycle. The regulation of the TCA cycle bypass during lipid mobilization was examined. Lipid mobilization in Brassica napus was initiated shortly after imbibition of the seed and proceeded until 2 d postimbibition, as measured by in vivo [1-14C]acetate feeding to whole seedlings. The activity of NAD+-isocitrate dehydrogenase (a decarboxylative enzyme) was not detected until 2 d postimbibition. RNA-blot analysis of B. napus seedlings demonstrated that the mRNA for NAD+-isocitrate dehydrogenase was present in dry seeds and that its level increased through the 4 d of the experiment. This suggested that NAD+-isocitrate dehydrogenase activity was regulated by posttranscriptional mechanisms during early seedling development but was controlled by mRNA level after the 2nd or 3rd d. The activity of fumarase (a component of the nonbypassed section of the TCA cycle) was low but detectable in B. napus seedlings at 12 h postimbibition, coincident with germination, and increased for the next 4 d. RNA-blot analysis suggested that fumarase activity was regulated primarily by the level of its mRNA during germination and early seedling development. It is concluded that posttranscriptional regulation of NAD+-isocitrate dehydrogenase activity is one mechanism of restricting carbon flux through the decarboxylative section of the TCA cycle during lipid mobilization in germinating oilseeds.


1   This research was supported by the National Science Foundation (grant IBN-9696154) and is a publication of the Iowa Agriculture Experiment Station.
2   Present address: Max-Planck-Institute fuer Chemische Oekologie, 07743, Jena, Germany.
*   Corresponding author; e-mail doliver{at}iastate.edu; fax 1-515-294-1337.

Plant Physiol. (1998) 117: 473-481
Copyright Clearance Center:   0032-0889/98/117/0473/09
© 1998 American Society of Plant Physiologists




This article has been cited by other articles:


Home page
Plant CellHome page
S. Penfield, Y. Li, A. D. Gilday, S. Graham, and I. A. Graham
Arabidopsis ABA INSENSITIVE4 Regulates Lipid Mobilization in the Embryo and Reveals Repression of Seed Germination by the Endosperm
PLANT CELL, August 1, 2006; 18(8): 1887 - 1899.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
A. Elorza, H. Roschzttardtz, I. Gomez, A. Mouras, L. Holuigue, A. Araya, and X. Jordana
A Nuclear Gene for the Iron-Sulfur Subunit of Mitochondrial Complex II is Specifically Expressed During Arabidopsis Seed Development and Germination
Plant Cell Physiol., January 1, 2006; 47(1): 14 - 21.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
G. R. Gray, A. R. Villarimo, C. L. Whitehead, and L. McIntosh
Transgenic Tobacco (Nicotiana tabacum L.) Plants with Increased Expression Levels of Mitochondrial NADP+-dependent Isocitrate Dehydrogenase: Evidence Implicating this Enzyme in the Redox Activation of the Alternative Oxidase
Plant Cell Physiol., October 15, 2004; 45(10): 1413 - 1425.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
C. Xiang, B. L. Werner, E'L. M. Christensen, and D. J. Oliver
The Biological Functions of Glutathione Revisited in Arabidopsis Transgenic Plants with Altered Glutathione Levels
Plant Physiology, June 1, 2001; 126(2): 564 - 574.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
D. C. Logan, A. H. Millar, L. J. Sweetlove, S. A. Hill, and C. J. Leaver
Mitochondrial Biogenesis during Germination in Maize Embryos
Plant Physiology, February 1, 2001; 125(2): 662 - 672.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1998 by the American Society of Plant Biologists