Previous Article | Next Article ![]()
Journal of Bacteriology, January 1999, p. 341-346, Vol. 181, No. 1
Division of Microbiology, GBF-National
Research Centre for Biotechnology, Braunschweig, Germany
Received 1 July 1998/Accepted 14 October 1998
The TecA broad-spectrum chlorobenzene dioxygenase of
Burkholderia sp. strain PS12 catalyzes the first step in
the mineralization of 1,2,4,5-tetrachlorobenzene. The catabolic genes
were localized on a small plasmid that belongs to the IncP
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Genetic and Biochemical Analyses of the
tec Operon Suggest a Route for Evolution of
Chlorobenzene Degradation Genes
incompatibility group. PCR analysis of the genetic environment of the
tec genes indicated high similarity to the
transposon-organized catabolic tcb chlorobenzene degradation genes of Pseudomonas sp. strain P51. Sequence
analysis of the regions flanking the tecA genes revealed an
upstream open reading frame (ORF) with high similarity to the
todF 2-hydroxy-6-oxo-2,4-heptadienoate hydrolase gene of
Pseudomonas putida F1 and a discontinuous downstream ORF
showing high similarity to the todE catechol
2,3-dioxygenase gene of strain F1. Both homologues in strain P51 exist
only as deletion remnants. We suggest that different genetic events
thus led to inactivation of the perturbing meta-cleavage
enzymes in strains P51 and PS12 during the evolution of efficient
chlorobenzene degradation pathways. Biochemical characterization of
TodF-like protein TlpF and a genetically refunctionalized TodE-like
protein, TlpE, produced in Escherichia coli provided data
consistent with the proposed relationships.
*
Corresponding author. Mailing address: Bereich
Mikrobiologie, AG Biodegradation, Gesellschaft für
Biotechnologische Forschung mbH, Mascheroder Weg 1, D-38124
Braunschweig, Germany. Phone: 49/(0)5 31/61 81-4 67. Fax: 49/(0)5 31/61
81-4 11. E-mail: dpi{at}gbf.de.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»