AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
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 Kleerebezem, R.
Right arrow Articles by Lettinga, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kleerebezem, R.
Right arrow Articles by Lettinga, G.
Agricola
Right arrow Articles by Kleerebezem, R.
Right arrow Articles by Lettinga, G.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, March 1999, p. 1152-1160, Vol. 65, No. 3
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Anaerobic Degradation of Phthalate Isomers by Methanogenic Consortia

Robbert Kleerebezem,* Look W. Hulshoff Pol, and Gatze Lettinga

Subdepartment of Environmental Technology, Department of Agricultural, Environmental, and Systems Technology, Wageningen Agricultural University, 6703 HD Wageningen, The Netherlands

Received 8 June 1998/Accepted 15 December 1998

Three methanogenic enrichment cultures, grown on ortho-phthalate, iso-phthalate, or terephthalate were obtained from digested sewage sludge or methanogenic granular sludge. Cultures grown on one of the phthalate isomers were not capable of degrading the other phthalate isomers. All three cultures had the ability to degrade benzoate. Maximum specific growth rates (µSmax) and biomass yields (YXtotS) of the mixed cultures were determined by using both the phthalate isomers and benzoate as substrates. Comparable values for these parameters were found for all three cultures. Values for µSmax and YXtotS were higher for growth on benzoate compared to the phthalate isomers. Based on measured and estimated values for the microbial yield of the methanogens in the mixed culture, specific yields for the phthalate and benzoate fermenting organisms were calculated. A kinetic model, involving three microbial species, was developed to predict intermediate acetate and hydrogen accumulation and the final production of methane. Values for the ratio of the concentrations of methanogenic organisms, versus the phthalate isomer and benzoate fermenting organisms, and apparent half-saturation constants (KS) for the methanogens were calculated. By using this combination of measured and estimated parameter values, a reasonable description of intermediate accumulation and methane formation was obtained, with the initial concentration of phthalate fermenting organisms being the only variable. The energetic efficiency for growth of the fermenting organisms on the phthalate isomers was calculated to be significantly smaller than for growth on benzoate.


* Corresponding author. Mailing address: Wageningen Agricultural University, Department of Agricultural, Environmental and Systems Technology, Subdepartment of Environmental Technology, "Biotechnion" Bomenweg 2, 6703 HD Wageningen, The Netherlands. Phone: (31-317) 483798. Fax: (31-317) 482108. E-mail: robbert.kleerebezem{at}algemeen.mt.wau.nl.


Applied and Environmental Microbiology, March 1999, p. 1152-1160, Vol. 65, No. 3
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 1999 by the American Society for Microbiology. All rights reserved.