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


     


Plant Physiology 51:158-173 (1973)
© 1973 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 (408)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Talmadge, K. W.
Right arrow Articles by Albersheim, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Talmadge, K. W.
Right arrow Articles by Albersheim, P.
Agricola
Right arrow Articles by Talmadge, K. W.
Right arrow Articles by Albersheim, P.
Articles

The Structure of Plant Cell Walls

I. The Macromolecular Components of the Walls of Suspension-cultured Sycamore Cells with a Detailed Analysis of the Pectic Polysaccharides 1

Kenneth W. Talmadge2, Kenneth Keegstra3, Wolfgang D. Bauer4 and Peter Albersheim5

a Department of Chemistry, University of Colorado, Boulder, Colorado 80302

This is the first in a series of papers dealing with the structure of cell walls isolated from suspension-cultured sycamore cells (Acer pseudoplatanus). These studies have been made possible by the availability of purified hydrolytic enzymes and by recent improvements in the techniques of methylation analysis. These techniques have permitted us to identify and quantitate the macromolecular components of sycamore cell walls. These walls are composed of 10% arabinan, 2% 3,6-linked arabinogalactan, 23% cellulose, 9% oligo-arabinosides (attached to hydroxyproline), 8% 4-linked galactan, 10% hydroxyproline-rich protein, 16% rhamnogalacturonan, and 21% xyloglucan.

The structures of the pectic polymers (the neutral arabinan, the neutral galactan, and the acidic rhamnogalacturonan) were obtained, in part, by methylation analysis of fragments of these polymers which were released from the sycamore walls by the action of a highly purified endopolygalacturonase. The data suggest a branched arabinan and a linear 4-linked galactan occurring as side chains on the rhamnogalacturonan. Small amounts or pieces of a xyloglucan, the wall hemicellulose, appear to be covalently linked to some of the galactan chains. Thus, the galactan appears to serve as a bridge between the xyloglucan and rhamnogalacturonan components of the wall.

The rhamnogalacturonan consists of an {alpha}-(1 -> 4)-linked galacturonan chain which is interspersed with 2-linked rhamnosyl residues. The rhamnosyl residues are not randomly distributed in the chain but probably occur in units of rhamnosyl- (1 -> 4)-galacturonosyl- (1 -> 2)-rhamnosyl. This sequence appears to alternate with a homogalacturonan sequence containing approximately 8 residues of 4-linked galacturonic acid. About half of the rhamnosyl residues are branched, having a substituent attached to carbon 4. This is likely to be the site of attachment of the 4-linked galactan.

The hydroxyprolyl oligo-arabinosides of the hydroxyproline-rich glycoprotein contain 3-linked, 2-linked, and terminal arabinosyl residues. The structure of the hydroxyprolyl oligo-arabinosides deduced from our methylation studies agrees with the structure reported for similar oligosaccharides.


2 National Science Foundation Predoctoral Fellow. Present address: Department of Biological Sciences, Princeton University, Princeton, N.J. 08540.

3 National Defense Education Act Predoctoral Fellow. Present address: Department of Biology, Massachusetts Institute of Technology, Cambridge, Mass. 02139.

4 Present address: MSU/AEC Plant Research Laboratory, Michigan State University, East Lansing, Mich. 48823.

5 To whom correspondence should be addressed.

1 Supported in part by Atomic Energy Commission Contract AT(11-1)-1426.




This article has been cited by other articles:


Home page
Plant Physiol.Home page
R. Naran, G. Chen, and N. C. Carpita
Novel Rhamnogalacturonan I and Arabinoxylan Polysaccharides of Flax Seed Mucilage
Plant Physiology, September 1, 2008; 148(1): 132 - 141.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
A. Alonso-Simon, P. Garcia-Angulo, A. Encina, J. L. Acebes, and J. Alvarez
Habituation of Bean (Phaseolus vulgaris) Cell Cultures to Quinclorac and Analysis of the Subsequent Cell Wall Modifications
Ann. Bot., June 1, 2008; 101(9): 1329 - 1339.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
Z. A. POPPER and S. C. FRY
Widespread Occurrence of a Covalent Linkage Between Xyloglucan and Acidic Polysaccharides in Suspension-cultured Angiosperm Cells
Ann. Bot., July 1, 2005; 96(1): 91 - 99.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1973 by the American Society of Plant Biologists