Previous Article | Next Article 
Journal of Bacteriology, November 2002, p. 5903-5911, Vol. 184, No. 21
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.21.5903-5911.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Carbon Monoxide Cycling by Desulfovibrio vulgaris Hildenborough
Gerrit Voordouw*
Max Planck Institute for Marine Microbiology, D-28359 Bremen, Germany
Received 20 May 2002/
Accepted 16 August 2002
Sulfate-reducing bacteria, like Desulfovibrio vulgaris Hildenborough, use the reduction of sulfate as a sink for electrons liberated in oxidation reactions of organic substrates. The rate of the latter exceeds that of sulfate reduction at the onset of growth, causing a temporary accumulation of hydrogen and other fermentation products (the hydrogen or fermentation burst). In addition to hydrogen, D. vulgaris was found to produce significant amounts of carbon monoxide during the fermentation burst. With excess sulfate, the hyd mutant (lacking periplasmic Fe-only hydrogenase) and hmc mutant (lacking the membrane-bound, electron-transporting Hmc complex) strains produced increased amounts of hydrogen from lactate and formate compared to wild-type D. vulgaris during the fermentation burst. Both hydrogen and CO were produced from pyruvate, with the hyd mutant producing the largest transient amounts of CO. When grown with lactate and excess sulfate, the hyd mutant also exhibited a temporary pause in sulfate reduction at the start of stationary phase, resulting in production of 600 ppm of headspace hydrogen and 6,000 ppm of CO, which disappeared when sulfate reduction resumed. Cultures with an excess of the organic electron donor showed production of large amounts of hydrogen, but no CO, from lactate. Pyruvate fermentation was diverse, with the hmc mutant producing 75,000 ppm of hydrogen, the hyd mutant producing 4,000 ppm of CO, and the wild-type strain producing no significant amount of either as a fermentation end product. The wild type was most active in transient production of an organic acid intermediate, tentatively identified as fumarate, indicating increased formation of organic fermentation end products in the wild-type strain. These results suggest that alternative routes for pyruvate fermentation resulting in production of hydrogen or CO exist in D. vulgaris. The CO produced can be reoxidized through a CO dehydrogenase, the presence of which is indicated in the genome sequence.
* Present address: Department of Biological Sciences, University of Calgary, 2500 University Dr. NW, Calgary, Alberta T2N 1N4, Canada. Phone: (403) 220-6388. Fax: (403) 289-9311. E-mail:
voordouw{at}ucalgary.ca.
Journal of Bacteriology, November 2002, p. 5903-5911, Vol. 184, No. 21
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.21.5903-5911.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Walker, C. B., He, Z., Yang, Z. K., Ringbauer, J. A. Jr., He, Q., Zhou, J., Voordouw, G., Wall, J. D., Arkin, A. P., Hazen, T. C., Stolyar, S., Stahl, D. A.
(2009). The Electron Transfer System of Syntrophically Grown Desulfovibrio vulgaris. J. Bacteriol.
191: 5793-5801
[Abstract]
[Full Text]
-
Caffrey, S. M., Park, H. S., Been, J., Gordon, P., Sensen, C. W., Voordouw, G.
(2008). Gene Expression by the Sulfate-Reducing Bacterium Desulfovibrio vulgaris Hildenborough Grown on an Iron Electrode under Cathodic Protection Conditions. Appl. Environ. Microbiol.
74: 2404-2413
[Abstract]
[Full Text]
-
Caffrey, S. M., Park, H.-S., Voordouw, J. K., He, Z., Zhou, J., Voordouw, G.
(2007). Function of Periplasmic Hydrogenases in the Sulfate-Reducing Bacterium Desulfovibrio vulgaris Hildenborough. J. Bacteriol.
189: 6159-6167
[Abstract]
[Full Text]
-
Tang, Y., Pingitore, F., Mukhopadhyay, A., Phan, R., Hazen, T. C., Keasling, J. D.
(2007). Pathway Confirmation and Flux Analysis of Central Metabolic Pathways in Desulfovibrio vulgaris Hildenborough using Gas Chromatography-Mass Spectrometry and Fourier Transform-Ion Cyclotron Resonance Mass Spectrometry. J. Bacteriol.
189: 940-949
[Abstract]
[Full Text]
-
Wildschut, J. D., Lang, R. M., Voordouw, J. K., Voordouw, G.
(2006). Rubredoxin:Oxygen Oxidoreductase Enhances Survival of Desulfovibrio vulgaris Hildenborough under Microaerophilic Conditions.. J. Bacteriol.
188: 6253-6260
[Abstract]
[Full Text]
-
Chhabra, S. R., He, Q., Huang, K. H., Gaucher, S. P., Alm, E. J., He, Z., Hadi, M. Z., Hazen, T. C., Wall, J. D., Zhou, J., Arkin, A. P., Singh, A. K.
(2006). Global Analysis of Heat Shock Response in Desulfovibrio vulgaris Hildenborough.. J. Bacteriol.
188: 1817-1828
[Abstract]
[Full Text]
-
Inagaki, S., Masuda, C., Akaishi, T., Nakajima, H., Yoshioka, S., Ohta, T., Pal, B., Kitagawa, T., Aono, S.
(2005). Spectroscopic and Redox Properties of a CooA Homologue from Carboxydothermus hydrogenoformans. J. Biol. Chem.
280: 3269-3274
[Abstract]
[Full Text]
-
Haveman, S. A., Greene, E. A., Stilwell, C. P., Voordouw, J. K., Voordouw, G.
(2004). Physiological and Gene Expression Analysis of Inhibition of Desulfovibrio vulgaris Hildenborough by Nitrite. J. Bacteriol.
186: 7944-7950
[Abstract]
[Full Text]
-
Roberts, G. P., Youn, H., Kerby, R. L.
(2004). CO-Sensing Mechanisms. Microbiol. Mol. Biol. Rev.
68: 453-473
[Abstract]
[Full Text]
-
Youn, H., Kerby, R. L., Conrad, M., Roberts, G. P.
(2004). Functionally Critical Elements of CooA-Related CO Sensors. J. Bacteriol.
186: 1320-1329
[Abstract]
[Full Text]
-
Elias, D. A., Suflita, J. M., McInerney, M. J., Krumholz, L. R.
(2004). Periplasmic Cytochrome c3 of Desulfovibrio vulgaris Is Directly Involved in H2-Mediated Metal but Not Sulfate Reduction. Appl. Environ. Microbiol.
70: 413-420
[Abstract]
[Full Text]
-
Haveman, S. A., Brunelle, V., Voordouw, J. K., Voordouw, G., Heidelberg, J. F., Rabus, R.
(2003). Gene Expression Analysis of Energy Metabolism Mutants of Desulfovibrio vulgaris Hildenborough Indicates an Important Role for Alcohol Dehydrogenase. J. Bacteriol.
185: 4345-4353
[Abstract]
[Full Text]