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Applied and Environmental Microbiology, February 2000, p. 493-498, Vol. 66, No. 2
Department of Chemical Engineering, The
University of Akron, Akron, Ohio 44325-3906
Received 16 August 1999/Accepted 3 November 1999
A strategy for sequential hydrocarbon bioremediation is proposed.
The initial O2-requiring transformation is effected by
aerobic resting cells, thus avoiding a high oxygen demand. The
oxygenated metabolites can then be degraded even under anaerobic
conditions when supplemented with a highly water-soluble alternative
electron acceptor, such as nitrate. To develop the new strategy, some
phenomena were studied by examining Pseudomonas aeruginosa
fermentation. The effects of dissolved oxygen (DO) concentration on
n-hexadecane biodegradation were investigated first. Under
microaerobic conditions, the denitrification rate decreased as the DO
concentration decreased, implying that the O2-requiring
reactions were rate limiting. The effects of different nitrate and
nitrite concentrations were examined next. When cultivated aerobically
in tryptic soy broth supplemented with 0 to 0.35 g of
NO2
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Degradation of n-Hexadecane and Its
Metabolites by Pseudomonas aeruginosa under Microaerobic
and Anaerobic Denitrifying Conditions
-N per liter, cells grew in all systems,
but the lag phase was longer in the presence of higher nitrite
concentrations. However, under anaerobic denitrifying conditions, even
0.1 g of NO2
-N per liter totally
inhibited cell growth. Growth was also inhibited by high nitrate
concentrations (>1 g of NO3
-N per liter).
Cells were found to be more sensitive to nitrate or nitrite inhibition
under denitrifying conditions than under aerobic conditions. Sequential
hexadecane biodegradation by P. aeruginosa was then
investigated. The initial fermentation was aerobic for cell growth and
hydrocarbon oxidation to oxygenated metabolites, as confirmed by
increasing dissolved total organic carbon (TOC) concentrations. The
culture was then supplemented with nitrate and purged with nitrogen
(N2). Nitrate was consumed rapidly initially. The live cell
concentration, however, also decreased. The aqueous-phase TOC level
decreased by about 40% during the initial active period but remained
high after this period. Additional experiments confirmed that only
about one-half of the derived TOC was readily consumable under
anaerobic denitrifying conditions.
*
Corresponding author. Mailing address: Department of
Chemical Engineering, The University of Akron, Akron, OH 44325-3906. Phone: (330) 972-7252. Fax: (330) 972-5856. E-mail:
LukeJu{at}UAkron.edu.
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