Previous Article | Next Article ![]()
Applied and Environmental Microbiology, March 2008, p. 1478-1484, Vol. 74, No. 5
0099-2240/08/$08.00+0 doi:10.1128/AEM.02236-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Geosciences, Guyot Hall, Princeton University, Princeton, New Jersey 08544,1 UMR 7517 (CNRS-ULP), EOST, 1 Rue Blessig, 67084 Strasbourg Cedex, France,2 Chemistry Department, PEI, Guyot Hall, Princeton University, Princeton, New Jersey 085443
Received 1 October 2007/ Accepted 1 January 2008
Vanadium is a cofactor in the alternative V-nitrogenase that is expressed by some N2-fixing bacteria when Mo is not available. We investigated the V requirements, the kinetics of V uptake, and the production of catechol compounds across a range of concentrations of vanadium in diazotrophic cultures of the soil bacterium Azotobacter vinelandii. In strain CA11.70, a mutant that expresses only the V-nitrogenase, V concentrations in the medium between 10–8 and 10–6 M sustain maximum growth rates; they are limiting below this range and toxic above. A. vinelandii excretes in its growth medium micromolar concentrations of the catechol siderophores azotochelin and protochelin, which bind the vanadate oxoanion. The production of catechols increases when V concentrations become toxic. Short-term uptake experiments with the radioactive isotope 49V show that bacteria take up the V-catechol complexes through a regulated transport system(s), which shuts down at high V concentrations. The modulation of the excretion of catechols and of the uptake of the V-catechol complexes allows A. vinelandii to precisely manage its V homeostasis over a range of V concentrations, from limiting to toxic.
Published ahead of print on 11 January 2008.
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»