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 Google Scholar
Google Scholar
Right arrow Articles by Lohmeier-Vogel, E. M.
Right arrow Articles by Vogel, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lohmeier-Vogel, E. M.
Right arrow Articles by Vogel, H. J.
Agricola
Right arrow Articles by Lohmeier-Vogel, E. M.
Right arrow Articles by Vogel, H. J.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, August 2001, p. 3549-3556, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3549-3556.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Phosphorus-31 Nuclear Magnetic Resonance Study of the Effect of Pentachlorophenol (PCP) on the Physiologies of PCP-Degrading Microorganisms

Elke M. Lohmeier-Vogel,1,* Kam T. Leung,dagger Hung Lee,2 Jack T. Trevors,2 and Hans J. Vogel1

Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada T2N 1N4,1 and Department of Environmental Biology, University of Guelph, Guelph, Ontario, Canada N1G 2W12

Received 4 January 2001/Accepted 15 May 2001

Free and agarose-encapsulated pentachlorophenol (PCP)-degrading Sphingomonas sp. isolates UG25 and UG30 were compared to Sphingomonas chlorophenolica ATCC 39723 with respect to the ability to degrade PCP. Pretreatment of the UG25 and UG30 strains with 50 µg of PCP per ml enabled the cells to subsequently degrade higher levels of this environmental pollutant. Similar treatment of ATCC 39723 cells had no effect on the level of PCP degraded by this strain. Phosphorus-31 nuclear magnetic resonance spectra of agarose-immobilized strains UG25 and UG30 grown in the absence of PCP showed that there was marked deenergization of the cells upon exposure to a nonlethal concentration of PCP (120 µg/ml). For example, no transmembrane pH gradient was observed, and the ATP levels were lower than the levels obtained in the absence of PCP. The transmembrane pH gradient and ATP levels were restored once the immobilized cells had almost completely degraded the PCP in the perfusion medium. PCP-pretreated cells, on the other hand, maintained their transmembrane pH gradient and ATP levels even in the presence of high levels of PCP. The ability of PCP-pretreated strain UG25 and UG30 cells to remain energized in the presence of PCP was shown to correlate with an altered membrane phospholipid profile; these cells had a higher concentration of cardiolipin than cells cultured in the absence of PCP. Strain ATCC 39723, which did not degrade higher levels of PCP after PCP pretreatment, did not show this response.


* Corresponding author. Mailing address: Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada T2N 1N4. Phone: (403) 220-8281. Fax: (403) 289-9311. E-mail: lohmeier{at}ucalgary.ca.

dagger Present address: Department of Biology, Lakehead University, Thunder Bay, Ontario, Canada P7B 5E1.


Applied and Environmental Microbiology, August 2001, p. 3549-3556, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3549-3556.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.