Vibriobactin, a siderophore from Vibrio cholerae

J Biol Chem. 1984 Jan 10;259(1):383-5.

Abstract

A novel siderophore (microbial iron transport compound) has been isolated from low iron cultures of Vibrio cholerae. Belonging to the catecholamide family of chelators, it has been shown to contain three residues of 2,3-dihydroxybenzoic acid and two residues of threonine. Both threonine moieties are present in the form of oxazoline rings. Furthermore, the polyamine backbone of the molecule was proved to be not spermidine, but the rare N-(3-aminopropyl)-1,3-diaminopropane, norspermidine. The structure of the new siderophore has been determined to be N-[3-(2,3-dihydroxybenzamido)propyl]-1, 3-bis[2,3-dihydroxyphenyl)-trans-5-methyl-2-oxazoline-4-carboxamido]prop ane. The compound has been given the trivial name vibriobactin. Mutants defective in the synthesis and utilization of vibriobactin were isolated. In an iron-limited environment V. cholerae was found to respond more strongly to vibriobactin, agrobactin, and ferrichrome than to enterobactin.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Catechols / analysis
  • Catechols / isolation & purification*
  • Chemical Phenomena
  • Chemistry
  • Ferrichrome / pharmacology
  • Iron / metabolism
  • Oxazoles*
  • Vibrio cholerae / analysis*
  • Vibrio cholerae / growth & development

Substances

  • Catechols
  • Oxazoles
  • Ferrichrome
  • vibriobactin
  • Iron