Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1387665 | Carbohydrate Research | 2014 | 6 Pages |
•The purified rhizobial carbohydrates were monofuntionalized with biotin tag.•The biotinylated cyclic β-glucans were synthesized through four steps.•Succinoglycans and monomers were biotinylated at the reducing sugar with one step.•The prepared neoglycoconjugate will be solid probes for study on symbiotic activity.
The cyclic β-glucans and succinoglycans produced by rhizobia are required for nodulation during symbiosis with legume hosts. However, only gene deletion analyses have been used to investigate their biological importance. For future studies on the physiological activity of those during symbiosis, biochemical methods need to be developed with separate carbohydrate compounds. Here, we isolated and purified rhizobial cellular carbohydrates using various chromatographic methods. Purified cyclic β-glucans, cyclosophoraoses, were monofunctionalized with biotin using the following three steps: tosylation, azidation, and amination. The mono-6-amino-cyclosophoraoses were linked with biotinamidohexanoic acid N-hydroxysuccinimide ester. Succinoglycans and monomers were tagged with biotinamidocaproyl hydrazide at the reducing sugar via reductive amination. The resulting biotinylated rhizobial carbohydrates were characterized by Fourier transform infrared and nuclear magnetic resonance spectroscopy, matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy, and electrospray ionization mass spectrometry. The resulting neoglycoconjugates can be used as solid probes to study putative plant receptors and for non-invasive imaging for in vivo tracing.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide