Phenazine antibiotic biosynthesis in Pseudomonas aureofaciens 30-84 is regulated by PhzR in response to cell density
Open Access
- 1 July 1994
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 176 (13) , 3966-3974
- https://doi.org/10.1128/jb.176.13.3966-3974.1994
Abstract
We have identified a gene that acts in trans to activate the expression of the phenazine biosynthetic genes in the biological control organism Pseudomonas aureofaciens 30-84. This gene, phzR (phenazine regulator), is located upstream of and divergently transcribed from the phenazine biosynthetic genes. Thus, the phenazine biosynthetic locus consists of at least two divergently transcribed operons. A functional phzR gene is required for phenazine production. The nucleotide sequence of phzR revealed an open reading frame of 723 nucleotides encoding a protein of ca. 27 kDa. The predicted amino acid sequence of PhzR has homology with other bacterial positive transcriptional activators, including LasR of Pseudomonas aeruginosa, LuxR of Vibrio fischerii, and TraR of Agrobacterium tumefaciens. The addition of cell-free supernatants from late-exponential-phase cultures of strain 30-84 resulted in expression of a genomic phzB:lacZ reporter strain at a lower cell density than normal, indicating the possible presence of an autoinducer. These results indicate that PhzR is a member of a two-component sensor-regulator family with known or predicted carboxy-terminal DNA-binding domains which regulates gene expression in response to environmental and cell density signals.Keywords
This publication has 36 references indexed in Scilit:
- Conjugation factor of Agrobacterium tumefaciens regulates Ti plasmid transfer by autoinductionNature, 1993
- Cloning and Heterologous Expression of the Phenazine Biosynthetic Locus fromPseudomonas aureofaciens30-84Molecular Plant-Microbe Interactions®, 1992
- Biological Control of Soilborne Plant Pathogens in the Rhizosphere with BacteriaAnnual Review of Phytopathology, 1988
- Mechanisms of inhibition of Gaeumannomyces graminis var. tritici by fluorescent pseudomonadsPlant Pathology, 1988
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- The pIC plasmid and phage vectors with versatile cloning sites for recombinant selection by insertional inactivationGene, 1984
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- A simple method for displaying the hydropathic character of a proteinJournal of Molecular Biology, 1982
- Structural identification of autoinducer of Photobacterium fischeri luciferaseBiochemistry, 1981
- Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.Proceedings of the National Academy of Sciences, 1980