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Plant Physiology 51:158-173 (1973) © 1973 American Society of Plant Biologists The Structure of Plant Cell WallsI. The Macromolecular Components of the Walls of Suspension-cultured Sycamore Cells with a Detailed Analysis of the Pectic Polysaccharides 1a 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 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:
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