Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 8 October 1999:
Vol. 286. no. 5438, pp. 306 - 309
DOI: 10.1126/science.286.5438.306

Reports

Anaerobic Microbes: Oxygen Detoxification Without Superoxide Dismutase

Francis E. Jenney Jr., Marc F. J. M. Verhagen, Xiaoyuan Cui, * Michael W. W. Adams dagger

Superoxide reductase from the hyperthermophilic anaerobe Pyrococcus furiosus uses electrons from reduced nicotinamide adenine dinucleotide phosphate, by way of rubredoxin and an oxidoreductase, to reduce superoxide to hydrogen peroxide, which is then reduced to water by peroxidases. Unlike superoxide dismutase, the enzyme that protects aerobes from the toxic effects of oxygen, SOR does not catalyze the production of oxygen from superoxide and therefore confers a selective advantage on anaerobes. Superoxide reductase and associated proteins are catalytically active 80°C below the optimum growth temperature (100°C) of P. furiosus, conditions under which the organism is likely to be exposed to oxygen.

Department of Biochemistry and Molecular Biology, Center for Metalloenzyme Studies, University of Georgia, Athens, GA 30602-7229, USA.
*   Present address: Natural Polymer Research, National Starch and Chemical Company, Bridgewater, NJ 08807 USA.

dagger    To whom correspondence should be addressed. E-mail: adams{at}bmb.uga.edu


Read the Full Text


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
The Archaeon Methanosarcina acetivorans Contains a Protein Disulfide Reductase with an Iron-Sulfur Cluster.
D. J. Lessner and J. G. Ferry (2007)
J. Bacteriol. 189, 7475-7484
   Abstract »    Full Text »    PDF »
Cell-Wide Responses to Low-Oxygen Exposure in Desulfovibrio vulgaris Hildenborough.
A. Mukhopadhyay, A. M. Redding, M. P. Joachimiak, A. P. Arkin, S. E. Borglin, P. S. Dehal, R. Chakraborty, J. T. Geller, T. C. Hazen, Q. He, et al. (2007)
J. Bacteriol. 189, 5996-6010
   Abstract »    Full Text »    PDF »
Assessing the Role of the Active-site Cysteine Ligand in the Superoxide Reductase from Desulfoarculus baarsii.
C. Mathe, C. O. Weill, T. A. Mattioli, C. Berthomieu, C. Houee-Levin, E. Tremey, and V. Niviere (2007)
J. Biol. Chem. 282, 22207-22216
   Abstract »    Full Text »    PDF »
An Enhancer Mutant of Arabidopsis salt overly sensitive 3 Mediates both Ion Homeostasis and the Oxidative Stress Response.
J. Zhu, X. Fu, Y. D. Koo, J.-K. Zhu, F. E. Jenney Jr., M. W. W. Adams, Y. Zhu, H. Shi, D.-J. Yun, P. M. Hasegawa, et al. (2007)
Mol. Cell. Biol. 27, 5214-5224
   Abstract »    Full Text »    PDF »
Raman-Assisted Crystallography Reveals End-On Peroxide Intermediates in a Nonheme Iron Enzyme.
G. Katona, P. Carpentier, V. Niviere, P. Amara, V. Adam, J. Ohana, N. Tsanov, and D. Bourgeois (2007)
Science 316, 449-453
   Abstract »    Full Text »    PDF »
Characterization of an Exceedingly Active NADH Oxidase from the Anaerobic Hyperthermophilic Bacterium Thermotoga maritima.
X. Yang and K. Ma (2007)
J. Bacteriol. 189, 3312-3317
   Abstract »    Full Text »    PDF »
Colloquium Paper: The plasma membrane Na+/H+ antiporter SOS1 interacts with RCD1 and functions in oxidative stress tolerance in Arabidopsis.
S. Katiyar-Agarwal, J. Zhu, K. Kim, M. Agarwal, X. Fu, A. Huang, and J.-K. Zhu (2006)
PNAS 103, 18816-18821
   Abstract »    Full Text »    PDF »
Detoxification of superoxide without production of H2O2: Antioxidant activity of superoxide reductase complexed with ferrocyanide.
F. P. Molina-Heredia, C. Houee-Levin, C. Berthomieu, D. Touati, E. Tremey, V. Favaudon, V. Adam, and V. Niviere (2006)
PNAS 103, 14750-14755
   Abstract »    Full Text »    PDF »
Rubredoxin:Oxygen Oxidoreductase Enhances Survival of Desulfovibrio vulgaris Hildenborough under Microaerophilic Conditions..
J. D. Wildschut, R. M. Lang, J. K. Voordouw, and G. Voordouw (2006)
J. Bacteriol. 188, 6253-6260
   Abstract »    Full Text »    PDF »
Genome of Rice Cluster I Archaea--the Key Methane Producers in the Rice Rhizosphere..
C. Erkel, M. Kube, R. Reinhardt, and W. Liesack (2006)
Science 313, 370-372
   Abstract »    Full Text »    PDF »
Comparison of Vertical Distributions of Prokaryotic Assemblages in the Anoxic Cariaco Basin and Black Sea by Use of Fluorescence In Situ Hybridization.
X. Lin, S. G. Wakeham, I. F. Putnam, Y. M. Astor, M. I. Scranton, A. Y. Chistoserdov, and G. T. Taylor (2006)
Appl. Envir. Microbiol. 72, 2679-2690
   Abstract »    Full Text »    PDF »
Adaptive Responses to Oxygen Stress in Obligatory Anaerobes Clostridium acetobutylicum and Clostridium aminovalericum.
S. Kawasaki, Y. Watamura, M. Ono, T. Watanabe, K. Takeda, and Y. Niimura (2005)
Appl. Envir. Microbiol. 71, 8442-8450
   Abstract »    Full Text »    PDF »
From The Cover: An archaeal antioxidant: Characterization of a Dps-like protein from Sulfolobus solfataricus.
B. Wiedenheft, J. Mosolf, D. Willits, M. Yeager, K. A. Dryden, M. Young, and T. Douglas (2005)
PNAS 102, 10551-10556
   Abstract »    Full Text »    PDF »
Rational Design of a Mononuclear Metal Site into the Archaeal Rieske-type Protein Scaffold.
T. Iwasaki, A. Kounosu, Y. Tao, Z. Li, J. E. Shokes, N. J. Cosper, T. Imai, A. Urushiyama, and R. A. Scott (2005)
J. Biol. Chem. 280, 9129-9134
   Abstract »    Full Text »    PDF »
In Vitro Reconstitution of an NADPH-Dependent Superoxide Reduction Pathway from Pyrococcus furiosus.
A. M. Grunden, F. E. Jenney Jr., K. Ma, M. Ji, M. V. Weinberg, and M. W. W. Adams (2005)
Appl. Envir. Microbiol. 71, 1522-1530
   Abstract »    Full Text »    PDF »
Complete genome sequence of the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1 and comparison with Pyrococcus genomes.
T. Fukui, H. Atomi, T. Kanai, R. Matsumi, S. Fujiwara, and T. Imanaka (2005)
Genome Res. 15, 352-363
   Abstract »    Full Text »    PDF »
Cold Shock of a Hyperthermophilic Archaeon: Pyrococcus furiosus Exhibits Multiple Responses to a Suboptimal Growth Temperature with a Key Role for Membrane-Bound Glycoproteins.
M. V. Weinberg, G. J. Schut, S. Brehm, S. Datta, and M. W. W. Adams (2005)
J. Bacteriol. 187, 336-348
   Abstract »    Full Text »    PDF »
Rubrerythrin from the Hyperthermophilic Archaeon Pyrococcus furiosus Is a Rubredoxin-Dependent, Iron-Containing Peroxidase.
M. V. Weinberg, F. E. Jenney Jr., X. Cui, and M. W. W. Adams (2004)
J. Bacteriol. 186, 7888-7895
   Abstract »    Full Text »    PDF »
Transcriptional Analysis of Biofilm Formation Processes in the Anaerobic, Hyperthermophilic Bacterium Thermotoga maritima.
M. A. Pysz, S. B. Conners, C. I. Montero, K. R. Shockley, M. R. Johnson, D. E. Ward, and R. M. Kelly (2004)
Appl. Envir. Microbiol. 70, 6098-6112
   Abstract »    Full Text »    PDF »
Oxidative Stress Response in an Anaerobic Hyperthermophilic Archaeon: Presence of a Functional Peroxiredoxin in Pyrococcus horikoshii.
R. Kawakami, H. Sakuraba, S. Kamohara, S. Goda, Y. Kawarabayasi, and T. Ohshima (2004)
J. Biochem. 136, 541-547
   Abstract »    Full Text »    PDF »
Neutron crystallographic study on rubredoxin from Pyrococcus furiosus by BIX-3, a single-crystal diffractometer for biomacromolecules.
K. Kurihara, I. Tanaka, T. Chatake, M. W. W. Adams, F. E. Jenney Jr., N. Moiseeva, R. Bau, and N. Niimura (2004)
PNAS 101, 11215-11220
   Abstract »    Full Text »    PDF »
Oxidative stress response in Clostridium perfringens.
D. Jean, V. Briolat, and G. Reysset (2004)
Microbiology 150, 1649-1659
   Abstract »    Full Text »    PDF »
Geobacter sulfurreducens Can Grow with Oxygen as a Terminal Electron Acceptor.
W. C. Lin, M. V. Coppi, and D. R. Lovley (2004)
Appl. Envir. Microbiol. 70, 2525-2528
   Abstract »    Full Text »    PDF »
A New Function of the Desulfovibrio vulgaris Hildenborough [Fe] Hydrogenase in the Protection against Oxidative Stress.
M. Fournier, Z. Dermoun, M.-C. Durand, and A. Dolla (2004)
J. Biol. Chem. 279, 1787-1793
   Abstract »    Full Text »    PDF »
Biochemical Properties and Regulated Gene Expression of the Superoxide Dismutase from the Facultatively Aerobic Hyperthermophile Pyrobaculum calidifontis.
T. Amo, H. Atomi, and T. Imanaka (2003)
J. Bacteriol. 185, 6340-6347
   Abstract »    Full Text »    PDF »
Kinetics of the Superoxide Reductase Catalytic Cycle.
J. P. Emerson, E. D. Coulter, R. S. Phillips, and D. M. Kurtz Jr. (2003)
J. Biol. Chem. 278, 39662-39668
   Abstract »    Full Text »    PDF »
Metabolic and Biochemical Responses of Probiotic Bacteria to Oxygen.
A. Talwalkar and K. Kailasapathy (2003)
J Dairy Sci 86, 2537-2546
   Abstract »    Full Text »    PDF »
Alkyl Hydroperoxide Reductase Dependent on Thioredoxin-Like Protein from Pyrococcus horikoshii.
Y. Kashima and K. Ishikawa (2003)
J. Biochem. 134, 25-29
   Abstract »    Full Text »    PDF »
Bioinorganic Chemistry Special Feature: How does cyanide inhibit superoxide reductase? Insight from synthetic FeIIIN4S model complexes.
J. Shearer, S. B. Fitch, W. Kaminsky, J. Benedict, R. C. Scarrow, and J. A. Kovacs (2003)
PNAS 100, 3671-3676
   Abstract »    Full Text »    PDF »
Bioinorganic Chemistry Special Feature: Nitric oxide binding at the mononuclear active site of reduced Pyrococcus furiosus superoxide reductase.
M. D. Clay, C. A. Cosper, F. E. Jenney Jr., M. W. W. Adams, and M. K. Johnson (2003)
PNAS 100, 3796-3801
   Abstract »    Full Text »    PDF »
Bioinorganic Chemistry Special Feature: An engineered two-iron superoxide reductase lacking the [Fe(SCys)4] site retains its catalytic properties in vitro and invivo.
J. P. Emerson, D. E. Cabelli, and D. M. Kurtz Jr. (2003)
PNAS 100, 3802-3807
   Abstract »    Full Text »    PDF »
Cloning and Expression of the Superoxide Dismutase Gene from the Obligate Anaerobic Bacterium Desulfovibrio vulgaris (Miyazaki F).
T. Nakanishi, H. Inoue, and M. Kitamura (2003)
J. Biochem. 133, 387-393
   Abstract »    Full Text »    PDF »
Hydrogen-Dependent Oxygen Reduction by Homoacetogenic Bacteria Isolated from Termite Guts.
H. I. Boga and A. Brune (2003)
Appl. Envir. Microbiol. 69, 779-786
   Abstract »    Full Text »    PDF »
Function of Oxygen Resistance Proteins in the Anaerobic, Sulfate-Reducing Bacterium Desulfovibrio vulgaris Hildenborough.
M. Fournier, Y. Zhang, J. D. Wildschut, A. Dolla, J. K. Voordouw, D. C. Schriemer, and G. Voordouw (2003)
J. Bacteriol. 185, 71-79
   Abstract »    Full Text »    PDF »
Unique Presence of a Manganese Catalase in a Hyperthermophilic Archaeon, Pyrobaculum calidifontis VA1.
T. Amo, H. Atomi, and T. Imanaka (2002)
J. Bacteriol. 184, 3305-3312
   Abstract »    Full Text »    PDF »
Polycationic photosensitizer conjugates: effects of chain length and Gram classification on the photodynamic inactivation of bacteria.
M. R. Hamblin, D. A. O'Donnell, N. Murthy, K. Rajagopalan, N. Michaud, M. E. Sherwood, and T. Hasan (2002)
J. Antimicrob. Chemother. 49, 941-951
   Abstract »    Full Text »    PDF »
Assembly of Photosystem I. I. INACTIVATION OF THE rubA GENE ENCODING A MEMBRANE-ASSOCIATED RUBREDOXIN IN THE CYANOBACTERIUM SYNECHOCOCCUS SP. PCC 7002 CAUSES A LOSS OF PHOTOSYSTEM I ACTIVITY.
G. Shen, J. Zhao, S. K. Reimer, M. L. Antonkine, Q. Cai, S. M. Weiland, J. H. Golbeck, and D. A. Bryant (2002)
J. Biol. Chem. 277, 20343-20354
   Abstract »    Full Text »    PDF »
Aerobic-Type Ribonucleotide Reductase in the Anaerobe Bacteroides fragilis.
D. Smalley, E. R. Rocha, and C. J. Smith (2002)
J. Bacteriol. 184, 895-903
   Abstract »    Full Text »    PDF »
The Mechanism of Superoxide Scavenging by Archaeoglobus fulgidus Neelaredoxin.
I. A. Abreu, L. M. Saraiva, C. M. Soares, M. Teixeira, and D. E. Cabelli (2001)
J. Biol. Chem. 276, 38995-39001
   Abstract »    Full Text »    PDF »
Radical SAM, a novel protein superfamily linking unresolved steps in familiar biosynthetic pathways with radical mechanisms: functional characterization using new analysis and information visualization methods.
H. J. Sofia, G. Chen, B. G. Hetzler, J. F. Reyes-Spindola, and N. E. Miller (2001)
Nucleic Acids Res. 29, 1097-1106
   Abstract »    Full Text »    PDF »
Leucine 41 is a gate for water entry in the reduction of Clostridium pasteurianum rubredoxin.
T. Min, C. E. Ergenekan, M. K. Eidsness, T. Ichiye, and C. Kang (2001)
Protein Sci. 10, 613-621
   Abstract »    Full Text »
Key Role for Sulfur in Peptide Metabolism and in Regulation of Three Hydrogenases in the Hyperthermophilic Archaeon Pyrococcus furiosus.
M. W. W. Adams, J. F. Holden, A. L. Menon, G. J. Schut, A. M. Grunden, C. Hou, A. M. Hutchins, F. E. Jenney Jr., C. Kim, K. Ma, et al. (2001)
J. Bacteriol. 183, 716-724
   Abstract »    Full Text »
Rubrerythrin and Rubredoxin Oxidoreductase in Desulfovibrio vulgaris: a Novel Oxidative Stress Protection System.
H. L. Lumppio, N. V. Shenvi, A. O. Summers, G. Voordouw, and D. M. Kurtz Jr. (2001)
J. Bacteriol. 183, 101-108
   Abstract »    Full Text »
The Role of Pyruvate Ferredoxin Oxidoreductase in Pyruvate Synthesis during Autotrophic Growth by the Wood-Ljungdahl Pathway.
C. Furdui and S. W. Ragsdale (2000)
J. Biol. Chem. 275, 28494-28499
   Abstract »    Full Text »    PDF »
Neelaredoxin, an Iron-binding Protein from the Syphilis Spirochete, Treponema pallidum, Is a Superoxide Reductase.
T. Jovanovic', C. Ascenso, K. R. O. Hazlett, R. Sikkink, C. Krebs, R. Litwiller, L. M. Benson, I. Moura, J. J. G. Moura, J. D. Radolf, et al. (2000)
J. Biol. Chem. 275, 28439-28448
   Abstract »    Full Text »    PDF »
Superoxide Reductase as a Unique Defense System against Superoxide Stress in the Microaerophile Treponema pallidum.
M. Lombard, D. Touati, M. Fontecave, and V. Niviere (2000)
J. Biol. Chem. 275, 27021-27026
   Abstract »    Full Text »    PDF »



ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)