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Journal of Bacteriology, July 2000, p. 3854-3857, Vol. 182, No. 13
Department of Microbiology, University of
Georgia, Athens, Georgia 30602-2605
Received 21 January 2000/Accepted 7 April 2000
Azotobacter vinelandii strains lacking the
nitrogenase-protective Shethna protein lost viability upon
carbon-substrate deprivation in the presence of oxygen. This viability
loss was dependent upon the N2-fixing status of cultures
(N2-fixing cells lost viability, while
non-N2-fixing cells did not) and on the ambient
O2 level. Supra-atmosheric O2 tensions
(40% partial pressure) decreased the viable cell number of the mutant
further, and the mutant had a slightly higher spontaneous mutation
frequency than the wild type in the high-O2 conditions.
Iron starvation conditions, which resulted in fourfold-reduced
superoxide dismutase levels, were also highly detrimental to the
viability of the protective protein mutants, but these conditions did
not affect the viability of the wild-type strain. Nitrogenase or other
powerful reductants associated with N2 fixation may be
sources of damaging partially reduced oxygen species, and the
production of such species are perhaps minimized by the Shethna protein.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Role of the Azotobacter vinelandii
Nitrogenase-Protective Shethna Protein in Preventing Oxygen-Mediated
Cell Death
*
Corresponding author. Mailing address: University of
Georgia, Department of Microbiology, 815 Biological Sciences Bldg.,
Athens, GA 30602-2605. Phone: (706) 542-2323. Fax: (706) 542-2674. E-mail: rmaier{at}arches.uga.edu.
Present address: The Monsanto Company, St. Louis, MO 63198.
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