The overall goal of the proposed project is to investigate the microbial role in the biogeochemical cycling of a) chromium and b) arsenic in the environment. a) We intend to examine the detoxification of Cr(VI) to Cr(III) coupled to the concomitant degradation of co-contaminant chemicals, such as toluene, phenol or p-cresol, likely to be found in mixed wastes in hazardous waste sites. We hypothesize that the microbial degradation of the aromatic organics can be coupled to Cr reduction, that this process is potentiated by biotic and abiotic found in the environment, and that microbial activity can affect the availability and transport of these organic and inorganic contaminants in and through the environment. B) In addition, we intend to examine the diversity of microbial communities involved in and the extent of microbial arsenic transformations. We hypothesize that microbial activity enhances the rate of arsenic reduction, oxidation and methylation under environmental condition. We will select, characterize, and develop molecular biomarkers for environmental strains of microorganisms (both aerobic and anaerobic) which can metabolize toluene, phenol and p-cresol coupled to chromate (Cr(VI)) reduction; in addition, we will screen our large strain collection which degrade these aromatic contaminants for Cr(VI) reduction. We will compare the rate, extent and stoichiometry of Cr reduction in microcosms and by the pure cultures, and determine the environmental factors affecting its reduction. We will determine if microbial oxidation of Cr(III) is relevant to the transport and cycling of Cr in the environment. We will examine community structure and changes, and flux of reactants and products in laboratory column microcosms with Cr(VI) reducing microbial communities which metabolize organize co-contaminants. In addition, we will seek a wide microbial diversity of arsenic reduction in environmental samples and to compare the rate and extent of arsenic reduction in microcosms and by novel isolated pure cultures. We will also determine if microbial oxidation of As(III) is relevant to the transport and cycling of As in the environment and we will determine the role of sulfate reducers in arsenic methylation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
1P42ES010344-01
Application #
6335591
Study Section
Special Emphasis Panel (ZES1-MAO-A (G2))
Project Start
2000-06-01
Project End
2005-03-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2000
Total Cost
$164,076
Indirect Cost
Name
New York University
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
Brocato, Jason; Costa, Max (2015) SATB1 and 2 in colorectal cancer. Carcinogenesis 36:186-91
Brocato, Jason; Wu, Fen; Chen, Yu et al. (2015) Association between sleeping hours and cardiometabolic risk factors for metabolic syndrome in a Saudi Arabian population. BMJ Open 5:e008590
Niu, Yingmei; DesMarais, Thomas L; Tong, Zhaohui et al. (2015) Oxidative stress alters global histone modification and DNA methylation. Free Radic Biol Med 82:22-8
Brocato, Jason; Hernandez, Michelle; Laulicht, Freda et al. (2015) In Vivo Exposures to Particulate Matter Collected from Saudi Arabia or Nickel Chloride Display Similar Dysregulation of Metabolic Syndrome Genes. J Toxicol Environ Health A 78:1421-36
Brocato, Jason; Chen, Danqi; Liu, Jianli et al. (2015) A Potential New Mechanism of Arsenic Carcinogenesis: Depletion of Stem-Loop Binding Protein and Increase in Polyadenylated Canonical Histone H3.1 mRNA. Biol Trace Elem Res 166:72-81
Brocato, Jason; Chervona, Yana; Costa, Max (2014) Molecular responses to hypoxia-inducible factor 1? and beyond. Mol Pharmacol 85:651-7
Brocato, Jason; Fang, Lei; Chervona, Yana et al. (2014) Arsenic induces polyadenylation of canonical histone mRNA by down-regulating stem-loop-binding protein gene expression. J Biol Chem 289:31751-64
Brocato, Jason; Costa, Max (2013) Basic mechanics of DNA methylation and the unique landscape of the DNA methylome in metal-induced carcinogenesis. Crit Rev Toxicol 43:493-514
Arita, Adriana; Muñoz, Alexandra; Chervona, Yana et al. (2013) Gene expression profiles in peripheral blood mononuclear cells of Chinese nickel refinery workers with high exposures to nickel and control subjects. Cancer Epidemiol Biomarkers Prev 22:261-9
Passantino, Lisa; Muñoz, Alexandra B; Costa, Max (2013) Sodium metavanadate exhibits carcinogenic tendencies in vitro in immortalized human bronchial epithelial cells. Metallomics 5:1357-67

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