Peer-Reviewed Journal Details
Mandatory Fields
Corkery, DM;Dobson, ADW
1998
September
Fems Microbiology Letters
Reverse transcription-PCR analysis of the regulation of ethylbenzene dioxygenase gene expression in Pseudomonas fluorescens CA-4
Validated
WOS: 6 ()
Optional Fields
ISOPROPYLBENZENE DEGRADATION GENES NUCLEOTIDE-SEQUENCE ESCHERICHIA-COLI PUTIDA STYRENE OXIDATION METABOLISM CLONING PLASMID CUMENE
166
171
176
Pseudomonas fluorescens strain CA-4 is a bioreactor isolate previously characterised by the presence of a side chain oxidation pathway for ethylbenzene breakdown. In this report a second pathway involving ethylbenzene ring dioxygenation has been identified in this strain. We examine here second substrate inhibition of the genes encoding the initial enzymes of this pathway, using reverse transcription (RT)-PCR. The genes of the ring-dioxygenation have been cloned and sequenced. They exhibit near identity to the gene clusters encoding the aromatic ring dioxygenase enzymes of two previously described isopropyl degrading strains, Pseudomonas sp. strain JR1 and P. fluorescens IP01. This dioxygenase pathway appears to be the major pathway for ethylbenzene degradation in this strain. The expression of these genes appears to be affected by the presence of second carbon substrates. Using RT-PCR we demonstrate that the negative effect of glutamate present in the growth medium together with ethylbenzene on the rate of ethylbenzene metabolism is mediated at the transcriptional level on the ethylbenzene dioxygenase genes. (C) 1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
AMSTERDAM
0378-1097
Grant Details