Abstract
Eight luxI-family gene promoters (luxI, cviI, ahlI, rhlI, cepI, phzI, traI and ppuI) were cloned in tandem, upstream a promoterless lacZ gene in a promoter probe vector yielding pMULTIAHLPROM. This unique construct is useful in determining whether a bacterial strain not producing N-acyl homoserine lactone signal molecules (AHLs) possesses orphan LuxR type proteins able to respond to AHLs and activate transcription from quorum sensing target genes. Using pMULTIAHLPROM, it was demonstrated that Enterobacter aerogenes possibly contains a LuxR-family orphan able to activate luxI-family promoters independently from AHLs.
Original language | English |
---|---|
Pages (from-to) | 273-275 |
Number of pages | 3 |
Journal | Journal of Microbiological Methods |
Volume | 73 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2008 |
Externally published | Yes |
Bibliographical note
Funding Information:L.S. and S.S. are supported by an ICGEB fellowship. V.V.'s laboratory in the ICGEB Biosafety Outstation in Ca'Tron is also supported by the Fondazione Cassamarca, Treviso, Italy.
Keywords
- Biosensor
- LuxR
- N-acyl homoserine lactone
- Plasmid
- Quorum sensing
ASJC Scopus subject areas
- Microbiology
- Molecular Biology
- Microbiology (medical)