Polar flagellin glycan metaheterogeneity of Aeromonas hydrophila strain ATCC 7966T
Fulton, K. M.; Mendoza-Barbera, E.; Tomas, J. M.; Twine, S. M.; Smith, J. C.; Merino, S.
Show abstract
Motile pathogens often rely upon flagellar motility as an essential virulence factor and in many species the structural flagellin protein is glycosylated. This post-translational modification has been shown to be necessary for proper folding of the flagellin structural proteins and proper function of the flagellar filament in a number of bacterial species. Aeromonas hydrophila is a ubiquitous aquatic pathogen with a constitutively expressed polar flagellum. Using a suite of mass spectrometry techniques, the flagellin FlaA and FlaB structural proteins of A. hydrophila strain ATCC 7966T were shown to be glycosylated with significant metaheterogeneity: heterologous glycans were observed with variable site occupancy. The penta- and hexa-saccharide glycan chains contained a previously unreported pseudaminic acid derivative with a mass of 422 Da as the linking sugar, followed in sequence by two hexoses, an N-acetylglucosamine derivative, a deoxy N-acetylglucosamine derivative, and sometimes an additional N-acetylglucosamine.
Matching journals
The top 12 journals account for 50% of the predicted probability mass.