The broad objective of this project is to advance the knowledge of fundamental processes involved in sequential anaerobic and aerobic PCB degradation. This interdisciplinary research should yield biotechnology that is based on sequential anaerobic-aerobic degradation and results in mineralization of a wide range of PCBs and therefore will reduce biological activities and toxicity of one of the most ubiquitous and troublesome cases of Superfund chemicals.
Specific aims of the proposed research are: (I) evaluation of the effect of FeSO4 on and enhancement of dechlorination of Aroclors and sediment associated PCBs by mixed cultures and enrichments of dechlorination of Aroclors and sediment associated PCBs by mixed cultures and enrichments; (II) evaluation of metabolic of metabolic rate and toxicity of PCB intermediates; (III) enhancement of recombinant degradative pathways for ortho-substituted PCBs; and (IV) elucidation of the composition and dynamics of mixed microbial populations involved in PCB degradation and manage combinations of populations for enhanced bioremediation. The proposed work builds on our recent discoveries that FeSO4 stimulates anaerobic dechlorination of Aroclor and that a single-step upgrading of pre-existing pathways with aromatic dechlorinases yields bacteria that now grow on some of the products of anaerobic PCB dechlorination. The stimulatory effect of FeSO4 will be further studied on (i) a wider combination of Aroclors and inocula, (ii) in situ dechlorination of field weathered PCBs in sediments, and (iii) the major individual dechlorination processes known to occur in situ. These efforts will enable production of more completely dechlorinated PCB mixtures with increased susceptibility to aerobic metabolism. To develop these aerobic phase of PCB bioremediation, recently engineered recombinant PCB pathways will be further enhanced to minimize accumulation of toxic intermediates and for better coordination of participating pathways. This should yield bacteria with improved growth on a wider array of anaerobically produced PCBs. A comprehensive study of diversity, dynamics and metabolic shifts within PCB degrading mixed communities will provide knowledge needed to advance further understanding of the molecular, population and environmental factors that control the environmental fate of PCBs in Superfund sites.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES004911-14
Application #
6579889
Study Section
Special Emphasis Panel (ZES1)
Project Start
2002-04-01
Project End
2003-03-31
Budget Start
Budget End
Support Year
14
Fiscal Year
2002
Total Cost
$204,127
Indirect Cost
Name
Michigan State University
Department
Type
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Nault, Rance; Doskey, Claire M; Fader, Kelly A et al. (2018) Comparison of Hepatic NRF2 and Aryl Hydrocarbon Receptor Binding in 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Treated Mice Demonstrates NRF2-Independent PKM2 Induction. Mol Pharmacol 94:876-884
Dornbos, Peter; LaPres, John J (2018) Incorporating population-level genetic variability within laboratory models in toxicology: From the individual to the population. Toxicology 395:1-8
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Interfacial Structure and Interaction of Kaolinite Intercalated with N-methylformamide Insight from Molecular Dynamics Modeling. Appl Clay Sci 158:204-210
Fader, Kelly A; Nault, Rance; Raehtz, Sandi et al. (2018) 2,3,7,8-Tetrachlorodibenzo-p-dioxin dose-dependently increases bone mass and decreases marrow adiposity in juvenile mice. Toxicol Appl Pharmacol 348:85-98
Zhang, Shuai; Liu, Qinfu; Cheng, Hongfei et al. (2018) Mechanism Responsible for Intercalation of Dimethyl Sulfoxide in Kaolinite: Molecular Dynamics Simulations. Appl Clay Sci 151:46-53
Zhang, Qiang; Li, Jin; Middleton, Alistair et al. (2018) Bridging the Data Gap From in vitro Toxicity Testing to Chemical Safety Assessment Through Computational Modeling. Front Public Health 6:261
Fader, K A; Nault, R; Kirby, M P et al. (2018) Corrigendum to ""Convergence of hepcidin deficiency, systemic iron overloading, heme accumulation, and REV-ERB?/? activation in aryl hydrocarbon receptor-elicited hepatotoxicity"" [Toxicol. Appl. Pharmacol. 321 (2017) 1-17]. Toxicol Appl Pharmacol 344:74
Konganti, Kranti; Ehrlich, Andre; Rusyn, Ivan et al. (2018) gQTL: A Web Application for QTL Analysis Using the Collaborative Cross Mouse Genetic Reference Population. G3 (Bethesda) 8:2559-2562
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Molecular Dynamics Simulation of Basal Spacing, Energetics, and Structure Evolution of a Kaolinite-Formamide Intercalation Complex and Their Interfacial Interaction. J Phys Chem C Nanomater Interfaces 122:3341-3349
Fader, Kelly A; Nault, Rance; Kirby, Mathew P et al. (2017) Convergence of hepcidin deficiency, systemic iron overloading, heme accumulation, and REV-ERB?/? activation in aryl hydrocarbon receptor-elicited hepatotoxicity. Toxicol Appl Pharmacol 321:1-17

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