AOBPreview published online on March 10, 2005
Annals of Botany, doi:10.1093/aob/mci113
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 College of Marine Studies and College of Agriculture and Natural Resources, University of Delaware, 700 Pilottown Road, Lewes, DE 19958, USA
* To whom correspondence should be addressed.
Background and Aims Plant growth involves pressure-driven cell enlargement generally accompanied by deposition of new cell wall. New polysaccharides are secreted by the plasma membrane but their subsequent entry into the wall is obscure. Therefore, polysaccharides and gold colloids of various sizes were presented to the inner wall face as though they were secreted by the plasma membrane. Methods Primary cell walls were isolated from growing internodes of Chara corallina and one end was attached to a glass capillary. Solutions of dextran or suspensions of gold colloids were pushed into the lumen by oil in the capillary. The oil did not enter the wall, and the solution or suspension was pressed against the inner wall face, pressurized at various artificial P (turgor pressure), and polymer or colloid movement through the wall was monitored. Key Results Interstices in the wall matrix had a diameter of about 4·6 nm measured at high P with gold colloids. Small solute (0·8 nm) readily moved through these interstices unaffected by P. Dextrans of 3·5 nm diameter moved faster at higher P while dextran of 9 nm scarcely entered unless high P was present. Dextran of 11 nm did not enter unless P was above a threshold, and dextran of 27 nm did not enter at P as high as 0·5 MPa. The walls filtered the dextrans, which became concentrated against the inner wall face, and most polymer movement occurred after P stabilized and bulk flow ended. Conclusions P created a steep gradient in concentration and mechanical force at the inner wall face that moved large polymers into small wall openings apparently by starting a polymer end or deforming the polymer mechanically at the inner wall face. This movement occurred at P generally accepted to extend the walls for growth.
Received August 12, 2004
Revised October 4, 2004
Accepted January 26, 2005
Article
Turgor Pressure Moves Polysaccharides into Growing Cell Walls of Chara corallina
JOHN S. BOYER, E-mail: boyer{at}cms.udel.edu
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
L. Zonia and T. Munnik Vesicle trafficking dynamics and visualization of zones of exocytosis and endocytosis in tobacco pollen tubes J. Exp. Bot., March 1, 2008; 59(4): 861 - 873. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Proseus and J. S. Boyer Tension required for pectate chemistry to control growth in Chara corallina J. Exp. Bot., December 1, 2007; 58(15-16): 4283 - 4292. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Wei and P. M. Lintilhac Loss of Stability: A New Look at the Physics of Cell Wall Behavior during Plant Cell Growth Plant Physiology, November 1, 2007; 145(3): 763 - 772. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. M. Kramer, N. L. Frazer, and T. I. Baskin Measurement of diffusion within the cell wall in living roots of Arabidopsis thaliana J. Exp. Bot., August 28, 2007; (2007) erm155v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Giovannelli, A. Deslauriers, G. Fragnelli, L. Scaletti, G. Castro, S. Rossi, and A. Crivellaro Evaluation of drought response of two poplar clones (Populusxcanadensis Monch 'I-214' and P. deltoides Marsh. 'Dvina') through high resolution analysis of stem growth J. Exp. Bot., August 11, 2007; (2007) erm117v2. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Proseus and J. S. Boyer Calcium pectate chemistry controls growth rate of Chara corallina J. Exp. Bot., December 1, 2006; 57(15): 3989 - 4002. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Proseus and J. S. Boyer Identifying cytoplasmic input to the cell wall of growing Chara corallina J. Exp. Bot., September 1, 2006; 57(12): 3231 - 3242. [Abstract] [Full Text] [PDF] |
||||

