Accurate Mass MS/MS/MS Analysis of Siderophores Ferrioxamine B and E1 by Collision-Induced Dissociation Electrospray Mass Spectrometry

Journal of the American Society for Mass Spectrometry

Volumn 26, Issue 11, 2015, Pages 1899-1902

  Sidebottom, Ashley M ^a   Karty, Jonathan A ^a   Carlson, Erin E ^a,b  

^a INDIANA UNIVERSITY   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Accurate mass; MS MS MS; Siderophore; Trihydroxamate

Indexed keywords

ACETYLATION; BINS; DISSOCIATION; ELECTROSPRAY IONIZATION; IRON; MASS SPECTROMETRY; SPECTROMETRY;

ACCURATE MASS; COLLISION INDUCED DISSOCIATION; DIAGNOSTIC FEATURES; ELECTROSPRAY MASS SPECTROMETRY; MS/MS/MS; SIDEROPHORES; TANDEM MASS SPECTROMETRY; TRIHYDROXAMATE;

IRON COMPOUNDS;

AMIDE; FERRIC ION; FERRIOXAMINE; OXIME; SIDEROPHORE; CYCLOPEPTIDE; DEFEROXAMINE; FERRIOXAMINE E;

ACETYLATION; ARTICLE; CHELATION; CHEMICAL BOND; COLLISIONALLY ACTIVATED DISSOCIATION; COVALENT BOND; CYCLIZATION; ELECTROSPRAY MASS SPECTROMETRY; NONHUMAN; PROTEIN QUATERNARY STRUCTURE; TANDEM MASS SPECTROMETRY; CHEMICAL STRUCTURE; CHEMISTRY; PROCEDURES;

DEFEROXAMINE; FERRIC COMPOUNDS; MODELS, MOLECULAR; PEPTIDES, CYCLIC; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; TANDEM MASS SPECTROMETRY;

EID: 84958184883     PISSN: 10440305     EISSN: 18791123     Source Type: Journal    
DOI: 10.1007/s13361-015-1242-7     Document Type: Article

References (15)

1. Sandy, M.; Butler, A.: Microbial iron acquisition: marine and terrestrial siderophores. Chem. Rev. 109, 4580-4595 (2009)
2. Helman, R.; Lawrence, G.D.: The increase in ferrioxamine B reduction potential with increasing acidity of the medium. Bioelectrochem. Bioenerg. 22, 187-196 (1989)
3. Beasley, F.D.; Vinés, E.D.; Grigg, J.C.; Zheng, Q.; Liu, S.; Lajoie, G.A.; Murphy, M.E.P.; Heinrichs, D.E.: Characterization of staphyloferrin A biosynthetic and transport mutants in Staphylococcus aureus. Mol. Microbiol. 72, 947-963 (2009)
4. Cornelis, P.; Dingemans, J.: Pseudomonas aeruginosa adapts its iron uptake strategies in function of the type of infections. Front. Cell. Infect. Microbiol. 3, 75 (2013)
5. Martinez, J.; Carter-Franklin, J.N.; Mann, E.L.; Martin, J.D.; Haygood, M.G.; Butler, A.: Structure and membrane affinity of a suite of amphiphilic siderophores produced by a marine bacterium. Proc. Natl. Acad. Sci. U. S. A. 100, 3754-3759 (2003)
6. Martin, J.D.; Ito, Y.; Howmann, V.V.; Haygood, M.G.; Butler, A.: Structure and membrane affinity of new amphiphilic siderophores produced by Ochrobactrum sp. sp18. J. Biol. Inorg. Chem. 11, 633-641 (2006)
7. Barry, S.M.; Challis, G.L.: Recent advances in siderophore biosynthesis. Curr. Opin. Chem. Biol. 13, 205-215 (2009)
8. Guaglitz, J.M.; Iinishi, A.; Ito, Y.; Butler, A.: Microbial tailoring of acyl peptidic siderophores. Biochemistry 53, 2624-2631 (2014)
9. Sidebottom, A.M.; Johnson, A.R.; Karty, J.A.; Trader, D.J.; Carlson, E.E.: Integrated metabolomics approach facilitates discovery of an unpredicted natural product suite from Streptomyces coelicolor M145. ACS Chem. Biol. 8, 2009-2016 (2013)
10. D' Onofrio, A.; Crawford, J.M.; Stewart, E.J.; Witt, K.; Gavrish, E.; Epstein, S.; Clardy, J.; Lewis, K.: Siderophores from neighboring organisms promote the growth of uncultured bacteria. Chem. Biol. 17, 254-264 (2010)
11. Gledhill, M.: Electrospray ionisation-mass spectrometry of hydroxamate siderophores. Analyst 126, 1359-1362 (2001)
12. Mawji, E.; Gledhill, M.; Worsfold, P.J.; Achterberg, E.P.: Collision-induced dissociation of three groups of hydroxamate siderophores: ferrioxamines, ferrichromes, and coprogens/fusigens. Rapid Commun. Mass Spectrom. 22, 2195-2202 (2008)
13. Roberts, A.A.; Schultz, A.W.; Kersten, R.D.; Dorrestein, P.C.; Moore, B.S.: Iron acquisition in the marine actiomycete genus Salinispora is controlled by the desferrioxamine family of siderophores. FEMS Microbiol. Lett. 335, 95-103 (2012)
14. 2+ solution. J. Mass Spectrom. 39, 752-761 (2004)
15. Spasojevíc, I.; Boukhalfa, H.; Stevens, R.D.; Crumbliss, A.L.: Aqueous solution speciation of Fe(III) complexes with dihydroxamate siderophores alcaligin and rhodotorulic acid and synthetic analoges using electrospray ionization mass spectrometry. Inorg. Chem. 40, 49-58 (2001)