salicylates and vulnibactin

salicylates has been researched along with vulnibactin* in 1 studies

Other Studies

1 other study(ies) available for salicylates and vulnibactin

Article	Year
Structure of vulnibactin, a new polyamine-containing siderophore from Vibrio vulnificus. Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 1994, Volume: 7, Issue:2 A new siderophore named vulnibactin has been isolated from low iron cultures of Vibrio vulnificus, a human pathogen. The structure was established as N-[3-(2,3-dihydroxybenzamido)propyl]-1,3-bis[2-(2-hydroxy-phenyl)- trans-5 - methyl-2-oxazoline-4-carboxamido]propane by a combination of acid hydrolysis, nuclear magnetic resonance spectroscopy and positive fast atom bombardment mass spectrometry. Vulnibactin is characterized as containing one residue of 2,3-dihydroxybenzoic acid as well as two residues of salicylic acid, both of which are involved in the formation of oxazoline rings with L-threonine bound to a norspermidine backbone. In addition, two other compounds with siderophore activity were purified and their structures were also determined. These two compounds provided further support for the structure of vulnibactin. Topics: Amides; Animals; Culture Media; Hydrolysis; Hydroxybenzoates; Magnetic Resonance Spectroscopy; Oxazoles; Salicylates; Salicylic Acid; Siderophores; Spectrometry, Mass, Fast Atom Bombardment; Vibrio	1994

Article

Year

Structure of vulnibactin, a new polyamine-containing siderophore from Vibrio vulnificus.

Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 1994, Volume: 7, Issue:2

A new siderophore named vulnibactin has been isolated from low iron cultures of Vibrio vulnificus, a human pathogen. The structure was established as N-[3-(2,3-dihydroxybenzamido)propyl]-1,3-bis[2-(2-hydroxy-phenyl)- trans-5 - methyl-2-oxazoline-4-carboxamido]propane by a combination of acid hydrolysis, nuclear magnetic resonance spectroscopy and positive fast atom bombardment mass spectrometry. Vulnibactin is characterized as containing one residue of 2,3-dihydroxybenzoic acid as well as two residues of salicylic acid, both of which are involved in the formation of oxazoline rings with L-threonine bound to a norspermidine backbone. In addition, two other compounds with siderophore activity were purified and their structures were also determined. These two compounds provided further support for the structure of vulnibactin.

Topics: Amides; Animals; Culture Media; Hydrolysis; Hydroxybenzoates; Magnetic Resonance Spectroscopy; Oxazoles; Salicylates; Salicylic Acid; Siderophores; Spectrometry, Mass, Fast Atom Bombardment; Vibrio

1994