Skip Navigation


JXB Advance Access originally published online on February 25, 2005
Journal of Experimental Botany 2005 56(413):985-995; doi:10.1093/jxb/eri092
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
56/413/985    most recent
eri092v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
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 ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (18)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Lee, S. H.
Right arrow Articles by Steudle, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, S. H.
Right arrow Articles by Steudle, E.
Agricola
Right arrow Articles by Lee, S. H.
Right arrow Articles by Steudle, E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

RESEARCH PAPER

Gating of aquaporins by low temperature in roots of chilling-sensitive cucumber and chilling-tolerant figleaf gourd

Seong Hee Lee1,2, Gap Chae Chung2 and Ernst Steudle1,*

1Lehrstuhl Pflanzenökologie, Universität Bayreuth, D-95440 Bayreuth, Germany
2Agricultural Plant Stress Research Center, Division of Applied Plant Science, College of Agriculture and Life Sciences, Chonnam National University, Gwangju 500-757, South Korea

* To whom correspondence should be addressed. Fax: +49 921 552564. E-mail: ernst.steudle{at}uni-bayreuth.de

Effects of low temperature (8 °C) on the hydraulic conductivity of young roots of a chilling-sensitive (cucumber, Cucumis sativus L.) and a chilling-resistant (figleaf gourd, Cucurbita ficifolia Bouché) crop have been measured at the levels of whole root systems (root hydraulic conductivity, Lpr) and of individual cortical cells (cell hydraulic conductivity, Lp). Exposure of roots to low temperature (LRT) for up to 6 d caused a stronger suberization of the endodermis in cucumber compared with figleaf gourd, but no development of exodermal Casparian bands in either species. Changes in anatomy after 6 d of LRT treatment corresponded with a reduction in hydrostatic root Lpr of cucumber roots by a factor of 24, and by a factor of 2 in figleaf gourd. In figleaf gourd, there was a reduction only in hydrostatic Lpr but not in osmotic Lpr suggesting that the activity of water channels was not much affected by LRT treatment in this species. Changes in cell Lp in response to chilling and recovery were similar to the root levels, although they were more intense at the root level. Activation energies (Ea) and Q10 of water flow as measured at the cell level were high in cucumber (Ea=109±13 kJ mol–1; Q10=4.8±0.7; n=6–10 cells), but small in figleaf gourd (Ea=11±2 kJ mol–1; Q10=1.2±0.1; n=6–10 cells). Roots of figleaf gourd recovered better from LRT treatment than those of cucumber. In figleaf gourd, recovery (at both the root and cell level) often resulted in Lp and Lpr values which were even bigger than the original, i.e. there was an overshoot in hydraulic conductivity. These effects were larger for osmotic (representing the cell-to-cell passage of water) than for hydrostatic Lpr. After a short-term (1 d) exposure to 8 °C followed by 1 d at 20 °C, hydrostatic Lpr of cucumber nearly recovered and that of figleaf gourd still remained higher due to the overshoot. By contrast, osmotic Lpr and cell Lp in both species remained high by a factor of 3 compared with the control, possibly due to an increased activity of water channels. After preconditioning of roots at LRT, increased hydraulic conductivity was completely inhibited by HgCl2 at both the root and cell levels. Different from figleaf gourd, recovery from chilling was not complete in cucumber after longer exposure to LRT. It is concluded that at LRT, both changes in the activity of aquaporins (AQPs) and alterations of root anatomy determine the water uptake in both species. The high temperature dependence of cell Lp in cucumber suggests conformational changes of AQPs during LRT treatment which result in channel closure and in a strong gating of AQP activity by low temperature. This mechanism is thought to be different from that in figleaf gourd where AQPs reacted in the conventional way, i.e. low temperature affected the mobility of water molecules in AQPs rather than their open/closed state, and Q10 was low.

Key words: Activation energy, aquaporins, cortical cells, cucumber, figleaf gourd, hydraulic conductivity, low root temperature


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Plant Cell PhysiolHome page
M. Murai-Hatano, T. Kuwagata, J. Sakurai, H. Nonami, A. Ahamed, K. Nagasuga, T. Matsunami, K. Fukushi, M. Maeshima, and M. Okada
Effect of Low Root Temperature on Hydraulic Conductivity of Rice Plants and the Possible Role of Aquaporins
Plant Cell Physiol., September 1, 2008; 49(9): 1294 - 1305.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
T. Knipfer and E. Steudle
Root hydraulic conductivity measured by pressure clamp is substantially affected by internal unstirred layers
J. Exp. Bot., May 1, 2008; 59(8): 2071 - 2084.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
J. Y. Jang, J. Y. Rhee, D. G. Kim, G. C. Chung, J. H. Lee, and H. Kang
Ectopic Expression of a Foreign Aquaporin Disrupts the Natural Expression Patterns of Endogenous Aquaporin Genes and Alters Plant Responses to Different Stress Conditions
Plant Cell Physiol., September 1, 2007; 48(9): 1331 - 1339.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
E. M. Herman, K. Rotter, R. Premakumar, G Elwinger, R. Bae, L. Ehler-King, S. Chen, and D. P. Livingston III
Additional freeze hardiness in wheat acquired by exposure to -3 {degrees}C is associated with extensive physiological, morphological, and molecular changes
J. Exp. Bot., November 1, 2006; 57(14): 3601 - 3618.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
T. Hewezi, M. Leger, W. El Kayal, and L. Gentzbittel
Transcriptional profiling of sunflower plants growing under low temperatures reveals an extensive down-regulation of gene expression associated with chilling sensitivity
J. Exp. Bot., September 1, 2006; 57(12): 3109 - 3122.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
A. J. Garthwaite, E. Steudle, and T. D. Colmer
Water uptake by roots of Hordeum marinum: formation of a barrier to radial O2 loss does not affect root hydraulic conductivity
J. Exp. Bot., February 1, 2006; 57(3): 655 - 664.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.