Probing the Impact of Ligand Binding on the Acyl-Homoserine Lactone-Hindered Transcription Factor EsaR of Pantoea stewartii subsp. stewartii

• Published in: Journal of Bacteriology 2011-11, Vol.193 (22), p.6315-6322
• Main Authors: Schu, Daniel J, Ramachandran, Revathy, Geissinger, Jared S, Stevens, Ann M
• Format: Article
• Language: English
• Subjects: Acyl-Butyrolactones - metabolism; Bacterial plant pathogens; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacteriology; Binding sites; Biological and medical sciences; Cells; corn; crosslinking; exopolysaccharides; Flowers & plants; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Bacterial; in vitro studies; Ligands; Microbiology; Miscellaneous; Molecular Sequence Data; Molecules; Pantoea - genetics; Pantoea - metabolism; Pantoea stewartii subsp. stewartii; Pathogens; Phytopathology. Animal pests. Plant and forest protection; promoter regions; Protein Binding; Proteins; proteolysis; quorum sensing; Signal Transduction; size exclusion chromatography; transcription factors; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 0021-9193; 1098-5530; 1067-8832
• DOI: 10.1128/JB.05956-11

The quorum-sensing regulator EsaR from Pantoea stewartii subsp. stewartii is a LuxR homologue that is inactivated by acyl-homoserine lactone (AHL). In the corn pathogen P. stewartii, production of exopolysaccharide (EPS) is repressed by EsaR at low cell densities. However, at high cell densities when high concentrations of its cognate AHL signal are present, EsaR is inactivated and derepression of EPS production occurs. Thus, EsaR responds to AHL in a manner opposite to that of most LuxR family members. Depending on the position of its binding site within target promoters, EsaR serves as either a repressor or activator in the absence rather than in the presence of its AHL ligand. The effect of AHL on LuxR homologues has been difficult to study in vitro because AHL is required for purification and stability. EsaR, however, can be purified without AHL enabling an in vitro analysis of the response of the protein to ligand. Western immunoblots and pulse-chase experiments demonstrated that EsaR is stable in vivo in the absence or presence of AHL. Limited in vitro proteolytic digestions of a biologically active His-MBP tagged version of EsaR highlighted intradomain and interdomain conformational changes that occur in the protein in response to AHL. Gel filtration chromatography of the full-length fusion protein and cross-linking of the N-terminal domain both suggest that this conformational change does not impact the multimeric state of the protein. These findings provide greater insight into the diverse mechanisms for AHL responsiveness found within the LuxR family.