Mutation analysis of the different tfd genes for degradation of chloroaromatic compounds in Ralstonia eutropha JMP134.

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Serval ID
serval:BIB_13E7A2859831
Type
Article: article from journal or magazin.
Collection
Publications
Title
Mutation analysis of the different tfd genes for degradation of chloroaromatic compounds in Ralstonia eutropha JMP134.
Journal
Archives of Microbiology
Author(s)
Laemmli C., Werlen C., van der Meer J.R.
ISSN
0302-8933 (Print)
ISSN-L
0302-8933
Publication state
Published
Issued date
2004
Volume
181
Number
2
Pages
112-121
Language
english
Abstract
Ralstonia eutropha JMP134 possesses two sets of similar genes for degradation of chloroaromatic compounds, tfdCDEFB (in short: tfdI cluster) and tfdDII CII EII FII BII (tfdII cluster). The significance of two sets of tfd genes for the organism has long been elusive. Here, each of the tfd genes in the two clusters on the original plasmid pJP4 was replaced by double recombination with a gene fragment in which a kanamycin resistance gene was inserted into the respective tfd gene's reading frame. The insertion mutants were all tested for growth on 2,4-dichlorophenoxyacetic acid (2,4-D), 2-methyl-4-chlorophenoxyacetic acid (MCPA), and 3-chlorobenzoate (3-CBA). None of the tfdDII CII EII FII BII genes appeared to be essential for growth on 2,4-D or on 3-CBA. Mutations in tfdC, tfdD and tfdF also did not abolish but only retarded growth on 2,4-D, indicating that they were redundant to some extent as well. Of all tfd genes tested, only tfdE and tfdB were absolutely essential, and interruption of those two reading frames abolished growth on 2,4-D, 3-CBA ( tfdE only), and MCPA completely. Interestingly, strains with insertion mutations in the tfdI cluster and those in tfdDII, tfdCII, tfdEII and tfdBII were severely effected in their growth on MCPA, compared to the wild-type. This indicated that not only the tfdI cluster but also the tfdII cluster has an essential function for R. eutropha during growth on MCPA. In contrast, insertion mutation of tfdDII resulted in better growth of R. eutropha JMP134 on 3-CBA, which is most likely due to the prevention of toxic metabolite production in the absence of TfdDII activity.
Keywords
2,4-Dichlorophenoxyacetic Acid/metabolism, 2-Methyl-4-chlorophenoxyacetic Acid/metabolism, Anti-Bacterial Agents/pharmacology, Bacterial Proteins/genetics, Bacterial Proteins/physiology, Biodegradation, Environmental, Carboxylic Ester Hydrolases/genetics, Carboxylic Ester Hydrolases/physiology, Chlorobenzoates/metabolism, Cupriavidus necator/drug effects, Cupriavidus necator/genetics, Dioxygenases, Drug Resistance, Bacterial/genetics, Gene Order, Genes, Bacterial, Intramolecular Lyases/genetics, Intramolecular Lyases/physiology, Kanamycin/pharmacology, Kanamycin Resistance/genetics, Mutagenesis, Insertional, Mutation, Oxygenases/genetics, Oxygenases/physiology, Recombination, Genetic, Transcription, Genetic
Pubmed
Web of science
Open Access
Yes
Create date
21/01/2008 14:35
Last modification date
01/10/2019 7:16
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