The destruction and transformation of almost all toxic and non-toxic organic compounds in the environment is highly dependent on microbial activity. Anaerobic habitats are widely distributed in soils, sediments, subsurface environments and groundwater and receive significant levels of contaminants. Transformations under anaerobic conditions, particularly of the refractory aromatic hydrocarbons such as the benzenes is a poorly understood process. It is proposed the anaerobic microbial degradation of benzene, toluene and xylenes may be an important process of detoxification or transformation of these toxic organic contaminants. Because microbial degradation is so widespread, the projects and metabolites of degradation, and not the parent compound, may in fact be major components by which human health is affected. Using protocols previously developed in our laboratory, three different anaerobic conditions, denitrifying, sulfate reducing and methanogenic, will be studied, which nitrate, sulfate and carbonate serve as electron acceptors and are reduced to nitrogen, sulfide and methane, respectively. The rate, extent and metabolites produced from benzene, toluene and xylenes under each reducing condition will be examined. Furthermore, the effect of additional inorganic toxicants such as chromate, mercury and methylmercury on the degradation process will be examined. The pathway for catabolism will be delineated for on or more of the compounds with regard to metabolites formed and the relationship between stoichiometry of substrate oxidation and reduction of inorganic electron acceptor. Pure cultures of anaerobic species mediating this transformation will be isolated for separate physiological genetic and biochemical studies. Enhancement of the degradative capabilities of selected anaerobic strains will be carried out by the transfer of catabolic genes whose gene products do not require oxygen. Strains will be further improve by transferring metal resistant genes into the degradative species. Results anticipated will contribute important new knowledge concerning the anaerobic metabolism and detoxification processes of hazardous chemicals which occur in the environment and will generate bacterial strains which may be useful for decontamination purposes.

Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
Sutherland, J E; Zhitkovich, A; Kluz, T et al. (2000) Rats retain chromium in tissues following chronic ingestion of drinking water containing hexavalent chromium. Biol Trace Elem Res 74:41-53
Corti, M; Snyder, C A (1998) Gender- and age-specific cytotoxic susceptibility to benzene metabolites in vitro. Toxicol Sci 41:42-8
Salnikow, K; Wang, S; Costa, M (1997) Induction of activating transcription factor 1 by nickel and its role as a negative regulator of thrombospondin I gene expression. Cancer Res 57:5060-6
Klein, C B; Costa, M (1997) DNA methylation, heterochromatin and epigenetic carcinogens. Mutat Res 386:163-80
Gong, Z; Evans, H L (1997) Effect of chelation with meso-dimercaptosuccinic acid (DMSA) before and after the appearance of lead-induced neurotoxicity in the rat. Toxicol Appl Pharmacol 144:205-14
Snyder, C A; Udasin, I; Waterman, S J et al. (1996) Reduced IL-6 levels among individuals in Hudson County, New Jersey, an area contaminated with chromium. Arch Environ Health 51:26-8
Corti, M; Snyder, C A (1996) Influences of gender, development, pregnancy and ethanol consumption on the hematotoxicity of inhaled 10 ppm benzene. Arch Toxicol 70:209-17
Garte, S J; Trachman, J; Crofts, F et al. (1996) Distribution of composite CYP1A1 genotypes in Africans, African-Americans and Caucasians. Hum Hered 46:121-7
Dowjat, W K; Huang, X; Cosentino, S et al. (1996) Peroxidase deficiency of nickel-transformed hamster cells correlates with their increased resistance to cytotoxicity of peroxides. Biometals 9:151-6
Kitahara, J; Yamanaka, K; Kato, K et al. (1996) Mutagenicity of cobalt and reactive oxygen producers. Mutat Res 370:133-40

Showing the most recent 10 out of 106 publications