Pseudomonas aeruginosa LasA: a second elastase under the transcriptional control of lasR
- 1 August 1991
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 5 (8) , 2003-2010
- https://doi.org/10.1111/j.1365-2958.1991.tb00822.x
Abstract
The full elastolytic phenotype of Pseudomonas aeruginosa requires lasB, the structural gene for elastase, its transcriptional activator lasR, and lasA. The lasB gene was insertionally inactivated with the omega fragment and this mutated gene introduced into the P. aeruginosa chromosome. Replacement of the wild-type gene with the inactivated gene was verified by Southern analysis and confirmed by lack of elastase antigen on Western blots and lack of activity in liquid assays. The mutant did, however, retain elastolytic activity on elastin plates. This residual activity was abolished by inactivation of lasB in PAO-E64, a lasA-deficient mutant, demonstrating that it was due to the lasA gene product. Northern analysis demonstrated that, like lasB, lasA is transcriptionally controlled by the lasR gene product.Keywords
This publication has 32 references indexed in Scilit:
- Ways of Assembling Complex Natural Products on Modular Nonribosomal Peptide Synthetases A list of abbreviations can be found at the end of the text.ChemBioChem, 2002
- Secretion, processing and activation of bacterial extracellular proteasesMolecular Microbiology, 1989
- Construction of broad-host-range vectors for general cloning and promoter selection in Pseudomonas and Escherichia coliGene, 1989
- Transformation ofPseudomonas aeruginosaby electroporationNucleic Acids Research, 1989
- A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxRJournal of Bacteriology, 1988
- POSITIVE CONTROL OF TRANSCRIPTION INITIATION IN BACTERIAAnnual Review of Genetics, 1984
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- A putative signal peptidase recognition site and sequence in eukaryotic and prokaryotic signal peptidesJournal of Molecular Biology, 1983
- A rapid alkaline extraction procedure for screening recombinant plasmid DNANucleic Acids Research, 1979
- Construction of plasmids carrying the cI gene of bacteriophage lambda.Proceedings of the National Academy of Sciences, 1976