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


     


Plant Physiology 82:511-517 (1986)
© 1986 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 (94)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Landsberg, E.-C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Landsberg, E.-C.
Agricola
Right arrow Articles by Landsberg, E.-C.
Articles

Function of Rhizodermal Transfer Cells in the Fe Stress Response Mechanism of Capsicum annuum L

Ernst-Christian Landsberg

Institut für Nutzpflanzenforschung, Pflanzenernährung, Technische Universität Berlin, Lentzeallee 55-57, 1000 Berlin 33, Federal Republic of Germany

A variety of red pepper (Capsicum annuum L., cv Yaglik) responds to Fe deficiency stress with simultaneously enhanced H+ extrusion, reduction of ferric ions and synthesis of malic and citric acid in a swollen subapical root zone densely covered with root hairs. It is demonstrated that these stress responses temporally coincide with the development of rhizodermal and hypodermal transfer cells in this root zone. During stress response the transfer cells show a marked autofluorescence which could arise from endogenous iron chelators of the phenolic acid type. The presence of organelle-rich cytoplasm which often exhibits rotational cytoplasmic streaming points to high physiological activity and makes these cells, with their increased plasmalemma surface, particularly well suited for the entire stress response mechanism. Since Fe stress-induced acidification is diminished by vanadate and erythrosin B, both specific inhibitors of plasmalemma ATPases, it seems reasonable to suppose that H+ pumping from transfer cells is activated by an ATPase located in their plasmamembrane. H+ extrusion is also shown to be inhibited by abscisic acid. Raised phosphoenolpyruvate carboxylase activity and simultaneous accumulation of malate in the swollen root zone point to the action of a pH stat preventing a detrimental rise in cytoplasmic pH of transfer cells during enhanced H+ extrusion. The simultaneous increase in citric acid concentration favors chelation of iron at the site of its uptake and thus ensures long distance transport to the areas of metabolic demand. A direct link between citrate accumulation and ferric ion reduction as proposed in recent literature further supports the crucial role of transfer cells in the response to Fe deficiency stress.





This article has been cited by other articles:


Home page
J Exp BotHome page
S. Santi and W. Schmidt
Laser microdissection-assisted analysis of the functional fate of iron deficiency-induced root hairs in cucumber
J. Exp. Bot., March 2, 2008; (2008) erm351v1.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
O. Thimm, B. Essigmann, S. Kloska, T. Altmann, and T. J. Buckhout
Response of Arabidopsis to Iron Deficiency Stress as Revealed by Microarray Analysis
Plant Physiology, November 1, 2001; 127(3): 1030 - 1043.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
A. Schikora and W. Schmidt
Iron Stress-Induced Changes in Root Epidermal Cell Fate Are Regulated Independently from Physiological Responses to Low Iron Availability
Plant Physiology, April 1, 2001; 125(4): 1679 - 1687.
[Abstract] [Full Text]


Home page
J Exp BotHome page
P. D. Nisi and G. Zocchi
Phosphoenolpyruvate carboxylase in cucumber (Cucumis sativus L.) roots under iron deficiency: activity and kinetic characterization
J. Exp. Bot., November 1, 2000; 51(352): 1903 - 1909.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
A. F. López-Millán, F. Morales, S. Andaluz, Y. Gogorcena, A. Abadía, J. D. L. Rivas, and J. Abadía
Responses of Sugar Beet Roots to Iron Deficiency. Changes in Carbon Assimilation and Oxygen Use
Plant Physiology, October 1, 2000; 124(2): 885 - 898.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
M. Watt and J. R. Evans
Proteoid Roots. Physiology and Development
Plant Physiology, October 1, 1999; 121(2): 317 - 324.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1986 by the American Society of Plant Biologists