Plant and Cell Physiology, 2002, Vol. 43, No. 12 1510-1517
© 2002 Oxford University Press
Utilization and Transport of Glucose in Olea Europaea Cell Suspensions
Centro de Ciências do Ambiente, Department of Biology, University of Minho, 4710-057 Braga, Portugal
Cell suspensions of Olea europaea var. Galega Vulgar grown in batch culture with 0.5% (w/v) glucose were able to transport D-[14C]glucose according to MichaelisMenten kinetics associated with a first-order kinetics. The monosaccharide carrier exhibited high affinity (Km
50 µM) and was able to transport D-glucose, D-fructose, D-galactose, D-xylose, 2-deoxy-D-glucose and 3-O-methyl-D-glucose, but not D-arabinose, D-mannitol or L-glucose. D-[14C]glucose uptake was associated with proton uptake, which also followed MichaelisMenten kinetics. The transport of 3-O-methyl-D-glucose was accumulative (40-fold, at pH 5.0) and the protonophore carbonyl cyanide m-chlorophenylhydrazone strongly inhibited sugar accumulation. The results were consistent with the involvement of a monosaccharide: proton symporter with a stoichiometry of 1 : 1. When cells were grown with 3% (w/v) glucose, the uptake of D-[14C]glucose followed first-order kinetics and monosaccharide:proton symporter activity was not detected. The value obtained for the permeability coefficient of hexoses in O. europaea cells supported the hypothesis that the first-order kinetics observed in 0.5% and 3% sugar-grown cells was produced exclusively by passive diffusion of the sugar. The results indicate that in O. europaea cells sugar levels have a regulatory effect on sugar transport, because the activity for monosaccharide transport was repressed by high sugar concentrations.
1 Corresponding author: E-mail, geros@bio.uminho.pt; Fax, + 351-253-678980.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
R.-C. Fan, C.-C. Peng, Y.-H. Xu, X.-F. Wang, Y. Li, Y. Shang, S.-Y. Du, R. Zhao, X.-Y. Zhang, L.-Y. Zhang, et al. Apple Sucrose Transporter SUT1 and Sorbitol Transporter SOT6 Interact with Cytochrome b5 to Regulate Their Affinity for Substrate Sugars Plant Physiology, August 1, 2009; 150(4): 1880 - 1901. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Pozueta-Romero, P. Gonzalez, E. Etxeberria, and J. Pozueta-Romero The Hyperbolic and Linear Phases of the Sucrose Accumulation Curve in Turnip Storage Cells Denote Carrier-mediated and Fluid Phase Endocytic Transport, Respectively J. Amer. Soc. Hort. Sci., July 1, 2008; 133(4): 612 - 618. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Conde, A. Agasse, P. Silva, R. Lemoine, S. Delrot, R. Tavares, and H. Geros OeMST2 Encodes a Monosaccharide Transporter Expressed throughout Olive Fruit Maturation Plant Cell Physiol., September 1, 2007; 48(9): 1299 - 1308. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Conde, P. Silva, A. Agasse, R. Lemoine, S. Delrot, R. Tavares, and H. Geros Utilization and Transport of Mannitol in Olea europaea and Implications for Salt Stress Tolerance Plant Cell Physiol., January 1, 2007; 48(1): 42 - 53. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Conde, A. Agasse, D. Glissant, R. Tavares, H. Geros, and S. Delrot Pathways of Glucose Regulation of Monosaccharide Transport in Grape Cells Plant Physiology, August 1, 2006; 141(4): 1563 - 1577. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Baroja-Fernandez, E. Etxeberria, F. J. Munoz, M. T. Moran-Zorzano, N. Alonso-Casajus, P. Gonzalez, and J. Pozueta-Romero An Important Pool of Sucrose Linked to Starch Biosynthesis is Taken up by Endocytosis in Heterotrophic Cells Plant Cell Physiol., April 1, 2006; 47(4): 447 - 456. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Azevedo, C. Conde, H. Geros, and R. M. Tavares The Non-host Pathogen Botrytis cinerea Enhances Glucose Transport in Pinus pinaster Suspension-cultured Cells Plant Cell Physiol., February 1, 2006; 47(2): 290 - 298. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Etxeberria, P. Gonzalez, P. Tomlinson, and J. Pozueta-Romero Existence of two parallel mechanisms for glucose uptake in heterotrophic plant cells J. Exp. Bot., July 1, 2005; 56(417): 1905 - 1912. [Abstract] [Full Text] [PDF] |
||||



