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Niklas (2000) defined plants as “photosynthetic eukaryotes,” thereby including brown, red, and green macroalgae and microalgae. These groups share several features, including the presence of a complex, dynamic, and polysaccharide-rich cell wall. Cell walls in eukaryotes are thought to have evolved by lateral transfer from cell wall-producing organisms (Niklas, 2004). Green and red algae originate from a primary endosymbiotic event with a cyanobacterium, which is thought to have occurred over 1,500 million years ago (Palmer et al., 2004). Even though extant cyanobacteria have cell walls that are based on a peptidoglycan-polysaccharide-lipopolysaccharide matrix and thus differ markedly from the polysaccharide-rich cell walls of plants, there is preliminary evidence that they may contain some similar polysaccharides (Hoiczyk and Hansel, 2000), and genes already involved in polysaccharide synthesis or those subsequently coopted into wall biosynthesis may have been transferred during endosymbiosis. Independent secondary endosymbiotic events subsequently gave rise to the Euglenozoa (which lack cell walls) and brown algae (which have cell walls; Palmer et al., 2004). Investigations of the diversity of wall composition, structure, and biosynthesis that include algae, therefore, may lend new insights into wall evolution (Niklas, 2004). peer-reviewed

A collection of 130 new plant cell wall glycan-directed monoclonal antibodies (mAbs) was generated with the aim of facilitating in-depth analysis of cell wall glycans. An enzyme-linked immunosorbent assay-based screen against a diverse panel of 54 plant polysaccharides was used to characterize the binding patterns of these new mAbs, together with 50 other previously generated mAbs, against plant cell wall glycans. Hierarchical clustering analysis was used to group these mAbs based on the polysaccharide recognition patterns observed. The mAb groupings in the resulting cladogram were further verified by immunolocalization studies in Arabidopsis (Arabidopsis thaliana) stems. The mAbs could be resolved into 19 clades of antibodies that recognize distinct epitopes present on all major classes of plant cell wall glycans, including arabinogalactans (both protein- and polysaccharide-linked), pectins (homogalacturonan, rhamnogalacturonan I), xyloglucans, xylans, mannans, and glucans. In most cases, multiple subclades of antibodies were observed to bind to each glycan class, suggesting that the mAbs in these subgroups recognize distinct epitopes present on the cell wall glycans. The epitopes recognized by many of the mAbs in the toolkit, particularly those recognizing arabinose- and/or galactose-containing structures, are present on more than one glycan class, consistent with the known structural diversity and complexity of plant cell wall glycans. Thus, these cell wall glycan-directed mAbs should be viewed and utilized as epitope-specific, rather than polymer-specific, probes. The current world-wide toolkit of approximately 180 glycan-directed antibodies from various laboratories provides a large and diverse set of probes for studies of plant cell wall structure, function, dynamics, and biosynthesis.