This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hallberg, K. B.
Right arrow Articles by Lindstrom, E. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hallberg, K. B.
Right arrow Articles by Lindstrom, E. B.

 Previous Article  |  Next Article 

J. Bacteriol., Jan 1996, 6-11, Vol 178, No. 1
Copyright © 1996, American Society for Microbiology

Reduced sulfur compound oxidation by Thiobacillus caldus

KB Hallberg, M Dopson and EB Lindstrom
Department of Applied Cell and Molecular Biology, Umea University, Sweden.

The oxidation of reduced inorganic sulfur compounds was studied by using resting cells of the moderate thermophile Thiobacillus caldus strain KU. The oxygen consumption rate and total oxygen consumed were determined for the reduced sulfur compounds thiosulfate, tetrathionate, sulfur, sulfide, and sulfite in the absence and in the presence of inhibitors and uncouplers. The uncouplers 2,4-dinitrophenol and carbonyl cyanide m-chlorophenyl-hydrazone had no affect on the oxidation of thiosulfate, suggesting that thiosulfate is metabolized periplasmically. In contrast, the uncouplers completely inhibited the oxidation of tetrathionate, sulfide, sulfur, and sulfite, indicating that these compounds are metabolized in the cytoplasm of T. caldus KU. N-Ethylmaleimide inhibited the oxidation of tetrathionate and thiosulfate at the stage of elemental sulfur, while 2-heptyl-4- hydroxyquinoline-N-oxide stopped the oxidation of thiosulfate, tetrathionate, and elemental sulfur at the stage of sulfite. The following intermediates in the oxidation of the sulfur compounds were found by using uncouplers and inhibitors: thiosulfate was oxidized to tetrathionate, elemental sulfur was formed during the oxidation of tetrathionate and sulfide, and sulfite was found as an intermediate of tetrathionate and sulfur metabolism. On the basis of these data we propose a model for the metabolism of the reduced inorganic sulfur compounds by T. caldus KU.


This article has been cited by other articles:

  • van Zyl, L. J., van Munster, J. M., Rawlings, D. E. (2008). Construction of arsB and tetH Mutants of the Sulfur-Oxidizing Bacterium Acidithiobacillus caldus by Marker Exchange. Appl. Environ. Microbiol. 74: 5686-5694 [Abstract] [Full Text]  
  • Rzhepishevska, O. I., Valdes, J., Marcinkeviciene, L., Gallardo, C. A., Meskys, R., Bonnefoy, V., Holmes, D. S., Dopson, M. (2007). Regulation of a Novel Acidithiobacillus caldus Gene Cluster Involved in Metabolism of Reduced Inorganic Sulfur Compounds. Appl. Environ. Microbiol. 73: 7367-7372 [Abstract] [Full Text]  
  • D'Imperio, S., Lehr, C. R., Breary, M., McDermott, T. R. (2007). Autecology of an Arsenite Chemolithotroph: Sulfide Constraints on Function and Distribution in a Geothermal Spring. Appl. Environ. Microbiol. 73: 7067-7074 [Abstract] [Full Text]  
  • Dopson, M., Lindström, E. B. (1999). Potential Role of Thiobacillus caldus in Arsenopyrite Bioleaching. Appl. Environ. Microbiol. 65: 36-40 [Abstract] [Full Text]