Journal of Bacteriology, September 2006, p. 6326-6334, Vol. 188, No. 17
0021-9193/06/$08.00+0 doi:10.1128/JB.00554-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Detection and Quantification of Superoxide Formed within the Periplasm of Escherichia coli
Sergei Korshunov and
James A. Imlay*
Department of Microbiology, University of Illinois, Urbana, Illinois 61801
Received 18 April 2006/
Accepted 12 June 2006
Many gram-negative bacteria harbor a copper/zinc-containing superoxide dismutase (CuZnSOD) in their periplasms. In pathogenic bacteria, one role of this enzyme may be to protect periplasmic biomolecules from superoxide that is released by host phagocytic cells. However, the enzyme is also present in many nonpathogens and/or free-living bacteria, including Escherichia coli. In this study we were able to detect superoxide being released into the medium from growing cultures of E. coli. Exponential-phase cells do not normally synthesize CuZnSOD, which is specifically induced in stationary phase. However, the engineered expression of CuZnSOD in growing cells eliminated superoxide release, confirming that this superoxide was formed within the periplasm. The rate of periplasmic superoxide production was surprisingly high and approximated the estimated rate of cytoplasmic superoxide formation when both were normalized to the volume of the compartment. The rate increased in proportion to oxygen concentration, suggesting that the superoxide is generated by the adventitious oxidation of an electron carrier. Mutations that eliminated menaquinone synthesis eradicated the superoxide formation, while mutations in genes encoding respiratory complexes affected it only insofar as they are likely to affect the redox state of menaquinone. We infer that the adventitious autoxidation of dihydromenaquinone in the cytoplasmic membrane releases a steady flux of superoxide into the periplasm of E. coli. This endogenous superoxide may create oxidative stress in that compartment and be a primary substrate of CuZnSOD.
* Corresponding author. Mailing address: University of Illinois, B103 Chemical and Life Sciences Laboratory, 601 S. Goodwin, Urbana, IL 61801. Phone: (217) 333-5812. Fax: (217) 244-6697. E-mail: jimlay{at}uiuc.edu.
Journal of Bacteriology, September 2006, p. 6326-6334, Vol. 188, No. 17
0021-9193/06/$08.00+0 doi:10.1128/JB.00554-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Ammendola, S., Pasquali, P., Pacello, F., Rotilio, G., Castor, M., Libby, S. J., Figueroa-Bossi, N., Bossi, L., Fang, F. C., Battistoni, A.
(2008). Regulatory and Structural Differences in the Cu,Zn-Superoxide Dismutases of Salmonella enterica and Their Significance for Virulence. J. Biol. Chem.
283: 13688-13699
[Abstract]
[Full Text]
-
Samaluru, H., SaiSree, L., Reddy, M.
(2007). Role of SufI (FtsP) in Cell Division of Escherichia coli: Evidence for Its Involvement in Stabilizing the Assembly of the Divisome. J. Bacteriol.
189: 8044-8052
[Abstract]
[Full Text]
-
Balashova, N. V., Park, D. H., Patel, J. K., Figurski, D. H., Kachlany, S. C.
(2007). Interaction between Leukotoxin and Cu,Zn Superoxide Dismutase in Aggregatibacter actinomycetemcomitans. Infect. Immun.
75: 4490-4497
[Abstract]
[Full Text]
-
Bellomio, A., Vincent, P. A., de Arcuri, B. F., Farias, R. N., Morero, R. D.
(2007). Microcin J25 Has Dual and Independent Mechanisms of Action in Escherichia coli: RNA Polymerase Inhibition and Increased Superoxide Production. J. Bacteriol.
189: 4180-4186
[Abstract]
[Full Text]
-
Lin, P.-C., Turk, K., Hase, C. C., Fritz, G., Steuber, J.
(2007). Quinone Reduction by the Na+-Translocating NADH Dehydrogenase Promotes Extracellular Superoxide Production in Vibrio cholerae. J. Bacteriol.
189: 3902-3908
[Abstract]
[Full Text]
-
Moreau, P. L.
(2007). The Lysine Decarboxylase CadA Protects Escherichia coli Starved of Phosphate against Fermentation Acids. J. Bacteriol.
189: 2249-2261
[Abstract]
[Full Text]
-
Harrison, A., Ray, W. C., Baker, B. D., Armbruster, D. W., Bakaletz, L. O., Munson, R. S. Jr.
(2007). The OxyR Regulon in Nontypeable Haemophilus influenzae. J. Bacteriol.
189: 1004-1012
[Abstract]
[Full Text]
Copyright © 2006 by the American Society for Microbiology. All rights reserved.