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« Previous AbstractBright mutants of Vibrio fischeri ES114 reveal conditions and regulators that control bioluminescence and expression of the lux operon    Next AbstractDrivers of Preference and Perception of Freshness in Roasted Peanuts (Arachis spp.) for European Consumers »

J Bacteriol


Title:Cyclic AMP receptor protein regulates pheromone-mediated bioluminescence at multiple levels in Vibrio fischeri ES114
Author(s):Lyell NL; Colton DM; Bose JL; Tumen-Velasquez MP; Kimbrough JH; Stabb EV;
Address:"Department of Microbiology, University of Georgia, Athens, Georgia, USA"
Journal Title:J Bacteriol
Year:2013
Volume:20130830
Issue:22
Page Number:5051 - 5063
DOI: 10.1128/JB.00751-13
ISSN/ISBN:1098-5530 (Electronic) 0021-9193 (Print) 0021-9193 (Linking)
Abstract:"Bioluminescence in Vibrio fischeri ES114 is activated by autoinducer pheromones, and this regulation serves as a model for bacterial cell-cell signaling. As in other bacteria, pheromone concentration increases with cell density; however, pheromone synthesis and perception are also modulated in response to environmental stimuli. Previous studies suggested that expression of the pheromone-dependent bioluminescence activator LuxR is regulated in response to glucose by cyclic AMP (cAMP) receptor protein (CRP) (P. V. Dunlap and E. P. Greenberg, J. Bacteriol. 164:45-50, 1985; P. V. Dunlap and E. P. Greenberg, J. Bacteriol. 170:4040-4046, 1988; P. V. Dunlap, J. Bacteriol. 171:1199-1202, 1989; and W. F. Friedrich and E. P. Greenberg, Arch. Microbiol. 134:87-91, 1983). Consistent with this model, we found that bioluminescence in V. fischeri ES114 is modulated by glucose and stimulated by cAMP. In addition, a Deltacrp mutant was approximately 100-fold dimmer than ES114 and did not increase luminescence in response to added cAMP, even though cells lacking crp were still metabolically capable of producing luminescence. We further discovered that CRP regulates not only luxR but also the alternative pheromone synthase gene ainS. We found that His-tagged V. fischeri CRP could bind sequences upstream of both luxR and ainS, supporting bioinformatic predictions of direct regulation at both promoters. Luminescence increased in response to cAMP if either the ainS or luxR system was under native regulation, suggesting cAMP-CRP significantly increases luminescence through both systems. Finally, using transcriptional reporters in transgenic Escherichia coli, we elucidated two additional regulatory connections. First, LuxR-independent basal transcription of the luxI promoter was enhanced by CRP. Second, the effect of CRP on the ainS promoter depended on whether the V. fischeri regulatory gene litR was also introduced. These results suggest an integral role for CRP in pheromone signaling that goes beyond sensing cell density"
Keywords:"Aliivibrio fischeri/*genetics/*metabolism Animals Bacterial Proteins/metabolism Cyclic AMP/metabolism DNA, Bacterial/metabolism Gene Deletion *Gene Expression Regulation, Bacterial Glucose/metabolism *Luminescence Pheromones/*metabolism Promoter Regions, ;"
Notes:"MedlineLyell, Noreen L Colton, Deanna M Bose, Jeffrey L Tumen-Velasquez, Melissa P Kimbrough, John H Stabb, Eric V eng Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. 2013/09/03 J Bacteriol. 2013 Nov; 195(22):5051-63. doi: 10.1128/JB.00751-13. Epub 2013 Aug 30"

 
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