Abstract
The promoter region of the Pseudomonas aeruginosa pilin gene has a high degree of similarity to the nitrogen-regulated promoters of enteric bacteria. These promoters are recognized by the alternative sigma factor of RNA polymerase, termed RpoN (NtrA or GlnF). This observation suggested that the P. aeruginosa pilin gene may be transcribed by the RpoN-containing RNA polymerase. We, therefore, cloned the RpoN gene from P. aeruginosa into Escherichia coli (where it formed a functional product) and used that cloned gene to construct a mutant of P. aeruginosa that was insertionally inactivated in its RpoN gene. This mutant failed to synthesize pilin, indicating that the RpoN sigma factor is required for transcription of the pilin gene.
MeSH Terms
Bacterial Outer Membrane Proteins/biosynthesis,genetics
Cloning, Molecular
DNA-Directed RNA Polymerases/genetics
Escherichia coli/genetics
Fimbriae Proteins
Fimbriae, Bacterial
Gene Expression Regulation
Mutation
Nucleic Acid Hybridization
Plasmids
Promoter Regions, Genetic
Pseudomonas aeruginosa/genetics
Sigma Factor/genetics
Transcription Factors/genetics
Transcription, Genetic
Transformation, Bacterial
beta-Galactosidase/genetics,metabolism
Chemicals
Bacterial Outer Membrane Proteins
Sigma Factor
Transcription Factors
Fimbriae Proteins
DNA-Directed RNA Polymerases
beta-Galactosidase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ishimoto K S
Department of Microbiology, School of Medicine, University of Washington, Seattle 98195.
Lory S
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