| Literature DB >> 26676799 |
Marie Dumont1, Arnaud Lehner1, Boris Vauzeilles2,3,4, Julien Malassis5, Alan Marchant6, Kevin Smyth5, Bruno Linclau5, Aurélie Baron2, Jordi Mas Pons2, Charles T Anderson7, Damien Schapman8, Ludovic Galas8, Jean-Claude Mollet1, Patrice Lerouge1.
Abstract
In plants, 3-deoxy-d-manno-oct-2-ulosonic acid (Kdo) is a monosaccharide that is only found in the cell wall pectin, rhamnogalacturonan-II (RG-II). Incubation of 4-day-old light-grown Arabidopsis seedlings or tobacco BY-2 cells with 8-azido 8-deoxy Kdo (Kdo-N3 ) followed by coupling to an alkyne-containing fluorescent probe resulted in the specific in muro labelling of RG-II through a copper-catalysed azide-alkyne cycloaddition reaction. CMP-Kdo synthetase inhibition and competition assays showing that Kdo and D-Ara, a precursor of Kdo, but not L-Ara, inhibit incorporation of Kdo-N3 demonstrated that incorporation of Kdo-N3 occurs in RG-II through the endogenous biosynthetic machinery of the cell. Co-localisation of Kdo-N3 labelling with the cellulose-binding dye calcofluor white demonstrated that RG-II exists throughout the primary cell wall. Additionally, after incubating plants with Kdo-N3 and an alkynated derivative of L-fucose that incorporates into rhamnogalacturonan I, co-localised fluorescence was observed in the cell wall in the elongation zone of the root. Finally, pulse labelling experiments demonstrated that metabolic click-mediated labelling with Kdo-N3 provides an efficient method to study the synthesis and redistribution of RG-II during root growth.Entities:
Keywords: Arabidopsis; BY-2 cells; Kdo-N3; cell wall; click chemistry; rhamnogalacturonan-II; technical advance
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Year: 2016 PMID: 26676799 DOI: 10.1111/tpj.13104
Source DB: PubMed Journal: Plant J ISSN: 0960-7412 Impact factor: 6.417