Localization and organization of phenol degradation genes ofPseudomonas putida strain H
- 1 March 1995
- journal article
- research article
- Published by Springer Nature in Molecular Genetics and Genomics
- Vol. 247 (2) , 240-246
- https://doi.org/10.1007/bf00705655
Abstract
The genetic organization of the DNA region encoding the phenol degradation pathway ofPseudomonas putida H has been investigated. This strain can utilize phenol or some of its methylated derivatives as its sole source of carbon and energy. The first step in this process is the conversion of phenol into catechol. Catechol is then further metabolized via themeta-cleavage pathway into TCA cycle intermediates. Genes encoding these enzymes are clustered on the plasmid pPGH1. A region of contiguous DNA spanning about 16 kb contains all of the genetic information necessary for inducible phenol degradation. The analysis of mutants generated by insertion of transposons and cassettes indicates that all of the catabolic genes are contained in a single operon. This codes for a multicomponent phenol hydroxylase andmeta-cleavage pathway enzymes. Catabolic genes are subject to positive control by the gene product(s) of a second locus.Keywords
This publication has 40 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Divergent evolution of chloroplast‐type ferredoxinsFEBS Letters, 1991
- Construction of a lacZ-kanamycin-resistance cassette, useful for site-directed mutagenesis and as a promoter probeGene, 1989
- Involvement of the plasmid pPGH1 in the phenol degradation ofPseudomonas putidastrain HFEMS Microbiology Letters, 1987
- Use of salicylate to estimate the “threshold” inducer level for de novo synthesis of the phenol‐degrading enzymes in Pseudomonas putida strain HJournal of Basic Microbiology, 1987
- Molecular cloning of the plasmid RP4 primase region in a multi-host-range tacP expression vectorGene, 1986
- Single-stranded DNA ‘blue’ T7 promoter plasmids: a versatile tandem promoter system for cloning and protein engineeringProtein Engineering, Design and Selection, 1986
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- Degradation of aniline and monochloroanilines byRhodococcus sp. An 117 and a pseudomonad: A comparative studyJournal of Basic Microbiology, 1983
- A complementation analysis of the restriction and modification of DNA in Escherichia coliJournal of Molecular Biology, 1969