This Article
Right arrow Full Text
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 Bressler, D. C.
Right arrow Articles by Fedorak, P. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bressler, D. C.
Right arrow Articles by Fedorak, P. M.
Agricola
Right arrow Articles by Bressler, D. C.
Right arrow Articles by Fedorak, P. M.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, February 2001, p. 821-826, Vol. 67, No. 2
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.2.821-826.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Purification, Stability, and Mineralization of 3-Hydroxy-2- Formylbenzothiophene, a Metabolite of Dibenzothiophene

David C. Bressler and Phillip M. Fedorak*

Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9

Received 2 October 2000/Accepted 29 November 2000

3-Hydroxy-2-formylbenzothiophene (HFBT) is a metabolite found in many bacterial cultures that degrade dibenzothiophene (DBT) via the Kodama pathway. The fate of HFBT in cultures and in the environment is unknown. In this study, HFBT was produced by a DBT-degrading bacterium and purified by sublimation. When stored in organic solvent or as a crystal, the HFBT slowly decomposed, yielding colored products. Two of these were identified as thioindigo and cis-thioindigo. The supernatant of the DBT-degrading culture contained thioindigo, which has not been reported previously as a product of DBT biodegradation. In mineral salts medium, HFBT was sufficiently stable to allow biodegradation studies with a mixed microbial culture over a 3- to 4-week period. High-performance liquid chromatography analyses showed that HFBT was removed from the medium. 2-Mercaptophenylglyoxalate, detected as benzothiophene-2,3-dione, was found in an HFBT-degrading mixed culture, and the former appears to be a metabolite of HFBT. This mixed culture also mineralized HFBT to CO2.


* Corresponding author. Mailing address: Department of Biological Sciences, University of Alberta, CW-405 Biological Sciences Bldg., Edmonton, Alberta, Canada T6G 2E9. Phone: (780) 492-3670. Fax: (780) 492-9234. E-mail: phil.fedorak{at}ualberta.ca.


Applied and Environmental Microbiology, February 2001, p. 821-826, Vol. 67, No. 2
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.2.821-826.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Young, R. F., Cheng, S. M., Fedorak, P. M. (2006). Aerobic Biodegradation of 2,2'-Dithiodibenzoic Acid Produced from Dibenzothiophene Metabolites. Appl. Environ. Microbiol. 72: 491-496 [Abstract] [Full Text]  
  • Bressler, D. C., Fedorak, P. M. (2001). Identification of Disulfides from the Biodegradation of Dibenzothiophene. Appl. Environ. Microbiol. 67: 5084-5093 [Abstract] [Full Text]