||Recruitment of tft and clc Biodegradative Pathway Genes: Modes of Evolution.
Coco, W. M. ;
Sangodkar, U. M. X. ;
Rothmel, R. K. ;
Chakrabarty, A. M. ;
||Illinois Univ. at the Medical Center, Chicago. Dept. of Microbiology and Immunology.;Environmental Protection Agency, Cincinnati, OH. Risk Reduction Engineering Lab.
Bacterial genes ;
2-4-5-trichlorophenoxyacetic acid ;
Pseudomonas cepacia ;
Pseudomonas putida ;
Deoxyribonucleic acids ;
Genetic transcription ;
||Some EPA libraries have a fiche copy filed under the call number shown.
||Pseudomonas putida can utilize a simple chlorinated compound 3-chlorocatechol (3-clc) through elaboration of a plasmid pAC27 encoded pathway. The clc genes are clustered as an operon termed clcABD. The positive regulatory gene clcR maps close to but is transcribed divergently from the clcABD operon. A similar genetic organization for catechol (Cat) degradation has been shown, where the catB gene of the catBC operon and its divergently transcribed catR regulatory gene show appreciable homology to clcB and clcR. This suggests that clc genes evolved by diverging from an extant, regulated catechol pathway. In contrast, a strain of P. cepacia (AC1100) was isolated from a chemostat under strong selection in the presence of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). This strain is characterized by: (1) marked genetic instability specific to the tft genes of the 2,4,5-T pathway, (2) several copies of the insertion sequence, RS1100, and (3) lack of detectable hybridization of either RS1100 or of the chq locus in the tft pathway with DNA from several species of pseudomonads.
||Pub. in Advances in Applied Biotechnology Series, 'Biotechnology and Biodegradation' Chapter 4, v4 p43-59. Sponsored by Environmental Protection Agency, Cincinnati, OH. Risk Reduction Engineering Lab.
|NTIS Title Notes
||Reprint: Recruitment of tft and clc Biodegradative Pathway Genes: Modes of Evolution.
||57F; 57K; 57B
||PC A03/MF A01