Skip Navigation


Plant and Cell Physiology Advance Access originally published online on August 27, 2006
Plant and Cell Physiology 2006 47(9):1309-1322; doi:10.1093/pcp/pcj101
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary data
Right arrow All Versions of this Article:
47/9/1309    most recent
pcj101v1
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 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 (7)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Malone, J. G.
Right arrow Articles by Kruger, N. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Malone, J. G.
Right arrow Articles by Kruger, N. J.
Agricola
Right arrow Articles by Malone, J. G.
Right arrow Articles by Kruger, N. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

The Response of Carbohydrate Metabolism in Potato Tubers to Low Temperature

Jacob G. Malone1, Valentina Mittova, R. George Ratcliffe and Nicholas J. Kruger*

Department of Plant Sciences, University of Oxford, South Parks Road, Oxford OX1 3RB, UK

* Corresponding author: E-mail, nick.kruger{at}plants.ox.ac.uk; Fax, +44-1865-275074.

This work investigates the possible causes of cold-induced sweetening in potato by examining the impact of low temperature on carbohydrate metabolism in mature tubers. Metabolism in tuber discs was monitored by determining the redistribution of radiolabel following incubation in [U-14C]glucose. Estimates of flux based on the specific activity of hexose phosphates established that while incubation at 4°C resulted in an immediate restriction in pathways of carbohydrate oxidation relative to activity at 25°C, there was no corresponding increase in flux to soluble sugars. In contrast, prior storage at low temperature stimulated flux to sugars at both 4 and 25°C. Comparison of 14CO2 release from specifically labeled glucose and gluconate fed to tuber discs at 4 and 25°C indicated that flux through glycolysis was preferentially restricted relative to the oxidative pentose phosphate pathway at low temperature, irrespective of prior storage temperature. However, the degree of randomization of label between positions C1 and C6 in the fructosyl moiety of sucrose following metabolism of [1-13C]glucose established that there was no preferential inhibition of the recycling of triose phosphates to hexose phosphates at low temperature. These results indicate that sugar accumulation in tubers during storage in the cold is not a direct consequence of a constraint in carbohydrate oxidation, despite preferential restriction of glycolysis at low temperature. It is concluded that the cold lability of enzymes catalyzing the conversion of fructose 6-phosphate to fructose 1,6-bisphosphate is not a major factor in cold-induced sweetening in plants and that this widely held hypothesis should be abandoned.

1 Present address: Division of Molecular Microbiology, Biozentrum, University of Basel, Klingelbergstrasse 91, 4056 Basel, Switzerland.


(Received June 1, 2006; Accepted August 3, 2006)
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
ANN BOT (LOND)Home page
D. L. Couldwell, R. Dunford, N. J. Kruger, D. C. Lloyd, R. G. Ratcliffe, and A. M. O. Smith
Response of cytoplasmic pH to anoxia in plant tissues with altered activities of fermentation enzymes: application of methyl phosphonate as an NMR pH probe
Ann. Bot., January 1, 2009; 103(2): 249 - 258.
[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.