role of exo-(1 to 4)-beta-galactanase in the mobilization of polysaccharides from the cotyledon cell walls of Lupinus angustifolius following germination

• Published in: Annals of botany Vol. 96; no. 3; pp. 435 - 444
• Main Authors: Buckeridge, M. S, Hutcheon, I. S, Reid, J. S. G
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.09.2005; Oxford Publishing Limited (England)
• Subjects: Acetates; beta-galactanase; beta-galactosidase; carbohydrates; Cell Wall - metabolism; Cell Wall - ultrastructure; cell wall components; cell wall porosity; Cell walls; Cotyledon - metabolism; Cotyledon - ultrastructure; Cotyledons; enzyme activity; enzyme-gold cytochemistry; Enzymes; exo-β-galactanase; Galactan; Galactans; Galactans - metabolism; Glycoside Hydrolases - metabolism; histochemistry; Lupinus - embryology; Lupinus - enzymology; Lupinus angustifolius; Mesophyll; Mesophyll cells; Monosaccharides; Monosaccharides - metabolism; nutrient transport; Original; pectin; pectins; plant anatomy; Polysaccharides; seed germination; seeds; ultrastructure; Uronic acids; β-galactosidase
• ISSN: 0305-7364; 1095-8290
• DOI: 10.1093/aob/mci192

BACKGROUND AND AIMS: The cotyledons of Lupinus angustifolius contain large amounts of cell wall storage polysaccharide (CWSP) composed mainly of (1 to 4)-beta-linked D-galactose residues in the form of branches attached to a rhamnogalacturonan core molecule. An exo-(1 to 4)-beta-galactanase with a very high specificity towards (1 to 4)-beta-linked D-galactan has been isolated from L. angustifolius cotyledons, and shown to vary (activity and specific protein) in step with CWSP mobilization. This work aimed to confirm the hypothesis that galactan is the main polymer retrieved from the wall during mobilization at the ultrastructural level, using the purified exo-galactanase as a probe. METHODS: Storage mesophyll cell walls ('ghosts') were isolated from the cotyledons of imbibed but ungerminated lupin seeds, and also from cotyledons of seedlings after the mobilization of the CWSP. The pure exo-(1 to 4)-beta-galactanase was coupled to colloidal gold particles and shown to be a specific probe for (1 to 4)-beta-D-galactan. They were used to localize galactan in ultrathin sections of L. angustifolius cotyledonary mesophyll tissue during CWSP mobilization. KEY RESULTS: On comparing the morphologies of isolated cell walls, the post-mobilization 'ghosts' did not have the massive wall-thickenings of pre-mobilization walls. Compositional analysis showed that the post-mobilization walls were depleted in galactose and, to a lesser extent, in arabinose. When pre-mobilization ghosts were treated with the pure exo-galactanase, they became morphologically similar to the post-mobilization ghosts. They were depleted of approximately 70% of the galactose residues that would have been mobilized in vivo, and retained all the other sugar residues originally present. Sharply defined electron-transparent wall zones or pockets are associated with CWSP mobilization, being totally free of galactan, whereas wall areas immediately adjacent to them were apparently undepleted. CONCLUSIONS: The exo-(1 to 4)-beta-galactanase is the principal enzyme involved in CWSP mobilization in lupin cotyledons in vivo. The storage walls dramatically change their texture during mobilization as most of the galactan is hydrolysed during seedling development.