Environmental release of a large number of synthetic chlorinated compounds in the form of herbicides/pesticides, solvents, refrigerants etc., has created major concerns with regard to their effect on human health because of the persistence of many such compounds. The persistence of these compounds is a reflection of the inability of natural microorganisms to utilize them as a sole source of carbon and energy. Many microorganisms can utilize simple chlorinated compounds such as 3-chlorobenzoate (3Cba) or 2,4-dichlorophenoxyacetate (2,4-D) as their sole carbon source but cannot utilize higher chlorinated forms such as 2,4,5-trichlorophenoxy acetic acid (2,4,5-T) and others. Under strong selection in a chemostat with 2,4,5-T as the only major source of carbon (directed evolution), it has been possible to isolate a strain of Pseudomonas cepacia AC1100 that can utilize 2,4,5-T as its sole source of carbon and energy. Molecular cloning of the genes both for 3Cba/2,4-D as well as 2,4,5,-T degradation has shown that while the chlorocatechol (clc) genes for 3Cba and 2,4-D dissimilation are highly homologous, the 2,4,5-T degradative (tft) genes show no homology with any of the genomic DNA of a large number of pseudomonads and other bacteria. The applicant proposes experiments to understand the nature of the tft genes and their products to determine exactly how 2,4,5-T is degraded by AC1100 and its mode of regulation. Sequencing and hyperexpression of a number of tft genes will be attempted to obtain information about the role of enzymes that allow efficient permeation of 2,4,5-T and its subsequent dechlorination and oxidation. Similarly, a regulatory protein involved in the positive regulation of catechol (cat) genes will be purified and its mode of binding with the promoter of the structural genes will be delineated to define the nature of this protein-DNA interaction for functional expression of the cat genes. These data would provide valuable information about the mode of evolution of structural and regulatory genes in nature as well as in chemostats in response to the release and availability of chlorinated compounds.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES004050-10
Application #
2153529
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1986-04-01
Project End
1996-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
10
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Hiraoka, Yoshinori; Granja, Ana Teresa; Fialho, Arsenio M et al. (2005) Human cytochrome c enters murine J774 cells and causes G1 and G2/M cell cycle arrest and induction of apoptosis. Biochem Biophys Res Commun 338:1284-90
Yamada, Tohru; Fialho, Arsenio M; Punj, Vasu et al. (2005) Internalization of bacterial redox protein azurin in mammalian cells: entry domain and specificity. Cell Microbiol 7:1418-31
Punj, Vasu; Bhattacharyya, Suchita; Saint-Dic, Djenann et al. (2004) Bacterial cupredoxin azurin as an inducer of apoptosis and regression in human breast cancer. Oncogene 23:2367-78
Yamada, Tohru; Hiraoka, Yoshinori; Das Gupta, Tapas K et al. (2004) Regulation of mammalian cell growth and death by bacterial redox proteins: relevance to ecology and cancer therapy. Cell Cycle 3:752-5
Yamada, Tohru; Hiraoka, Yoshinori; Das Gupta, Tapas K et al. (2004) Rusticyanin, a bacterial electron transfer protein, causes G1 arrest in J774 and apoptosis in human cancer cells. Cell Cycle 3:1182-7
Hiraoka, Yoshinori; Yamada, Tohru; Goto, Masatoshi et al. (2004) Modulation of mammalian cell growth and death by prokaryotic and eukaryotic cytochrome c. Proc Natl Acad Sci U S A 101:6427-32
Yamada, Tohru; Hiraoka, Yoshinori; Ikehata, Masateru et al. (2004) Apoptosis or growth arrest: Modulation of tumor suppressor p53's specificity by bacterial redox protein azurin. Proc Natl Acad Sci U S A 101:4770-5
Chakrabarty, A M (2003) Patenting life forms: yesterday, today, and tomorrow. Adv Genet 50:3-11; discussion 507-10
Punj, Vasu; Das Gupta, Tapas K; Chakrabarty, Ananda M (2003) Bacterial cupredoxin azurin and its interactions with the tumor suppressor protein p53. Biochem Biophys Res Commun 312:109-14
Punj, Vasu; Sharma, Rachna; Zaborina, Olga et al. (2003) Energy-generating enzymes of Burkholderia cepacia and their interactions with macrophages. J Bacteriol 185:3167-78

Showing the most recent 10 out of 51 publications