Inhibitors of autoinducer transporters
The present invention relates to the discovery of the lsr operon, the genes therein, and the polypeptides encoded by these genes. The present invention also includes strains with altered expression levels of the polypeptides encoded by the genes and the lsr operon relative to wild type cells. In some embodiments, the strains express a transporter that transports an autoinducer into the cell at a level higher than that of wild type cells. The present invention also includes methods for identifying compounds that modulate the transport of the autoinducer into cells.
1. An isolated bacterial strain having an increased expression level of a transporter relative to a wildtype strain wherein the transporter transports a pentanedione autoinducer into the strain and wherein the transporter comprises at least one polypeptide having at least 80% amino acid identity using a BLAST search or FASTA version 3.0t78 algorithm with the default parameters, or equivalent search to a peptide selected from the group consisting of SEQ ID NO. 37, SEQ ID NO. 38, SEQ ID NO. 39, and SEQ ID NO. 40, and wherein the autoinducer can interact with the Vibrio harveyi LuxP-LuxQ protein complex, thereby inducing Vibric harveyi bioluminescence.
2. The strain of claim 1 , wherein the strain comprises at least one synthetic vector from which one or more of the transporter polypeptides are expressed.
3. The strain of claim 1 , wherein the transporter comprises polypeptides having at least 80% amino acid identity using a BLASTP, BLASTX, or TBLASTN with the default parameters to SEQ ID NO. 37, SEQ ID NO. 38, SEQ ID NO. 39, and SEQ ID NO. 40.
4. The strain of claim 1 , wherein the strain comprises a mutation in a LsrR repressor gene that increases the expression level of the transporter.
5. The strain of claim 1 , wherein the autoinducer is 4,5-dihydroxy-2,3-pentanedione.
6. The strain of claim 1 , wherein the strain is within a species selected from the group consisting of S. typhimurium and E. coli.