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Applied and Environmental Microbiology, September 1998, p. 3300-3304, Vol. 64, No. 9
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Aerobic Growth on Nitroglycerin as the Sole Carbon, Nitrogen, and Energy Source by a Mixed Bacterial Culture

John V. Accashian,1,dagger Robert T. Vinopal,2 Byung-Joon Kim,3 and Barth F. Smets1,2,*

Environmental Engineering Program, Department of Civil and Environmental Engineering, University of Connecticut, Storrs, Connecticut 06269-20371; Microbiology Program, Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269-30442; and U.S. Army Construction Engineering Research Lab, Champaign, Illinois 61820-13053

Received 4 March 1998/Accepted 17 June 1998

Nitroglycerin (glycerol trinitrate [GTN]), an explosive and vasodilatory compound, was metabolized by mixed microbial cultures from aeration tank sludge previously exposed to GTN. Aerobic enrichment cultures removed GTN rapidly in the absence of a supplemental carbon source. Complete denitration of GTN, provided as the sole C and N source, was observed in aerobic batch cultures and proceeded stepwise via the dinitrate and mononitrate isomers, with successive steps occurring at lower rates. The denitration of all glycerol nitrate esters was found to be concomitant, and 1,2-glycerol dinitrate (1,2-GDN) and 2-glycerol mononitrate (2-GMN) were the primary GDN and GMN isomers observed. Denitration of GTN resulted in release of primarily nitrite-N, indicating a reductive denitration mechanism. Biomass growth at the expense of GTN was verified by optical density and plate count measurements. The kinetics of GTN biotransformation were 10-fold faster than reported for complete GTN denitration under anaerobic conditions. A maximum specific growth rate of 0.048 ± 0.005 h-1 (mean ± standard deviation) was estimated for the mixed culture at 25°C. Evidence of GTN toxicity was observed at GTN concentrations above 0.3 mM. To our knowledge, this is the first report of complete denitration of GTN used as a primary growth substrate by a bacterial culture under aerobic conditions.


* Corresponding author. Mailing address: Environmental Engineering Program, Department of Civil and Environmental Engineering, University of Connecticut, Storrs, CT 06269-2037. Phone: (860) 486-2270. Fax: (860) 486-2298. E-mail: bsmets{at}engr.uconn.edu.

dagger Present address: Camp Dresser & McKee, Denver, CO 80202.


Applied and Environmental Microbiology, September 1998, p. 3300-3304, Vol. 64, No. 9
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Marshall, S. J., Krause, D., Blencowe, D. K., White, G. F. (2004). Characterization of Glycerol Trinitrate Reductase (NerA) and the Catalytic Role of Active-Site Residues. J. Bacteriol. 186: 1802-1810 [Abstract] [Full Text]  
  • Marshall, S. J., White, G. F. (2001). Complete Denitration of Nitroglycerin by Bacteria Isolated from a Washwater Soakaway. Appl. Environ. Microbiol. 67: 2622-2626 [Abstract] [Full Text]