Sporulation is a mechanism that microorganisms have developed for survival under adverse conditions. The process follows an energy-intensive pathway with the activation or repression of numerous specific genes in a temporal and spatial sequence resulting in the production of a highly differentiated structure. The phosphorelay is a complex signal transduction system that governs the onset of sporulation initiation in Bacillus subtilis by responding to a myriad of positive and negative signals and integrating them into the most appropriate response. Negative inputs on the response regulators SpoOF and Spo0A of the phosphorelay are interpreted by the Rap and Spo0E families of phosphatases, respectively. The phosphatase genes are induced by physiological conditions antithetical to sporulation. Additionally, each Rap activity is inhibited by a specific pentapeptide which is generated from the processing of corresponding phr gene products.
The aim of this proposal is the detailed molecular, biochemical andI structural characterization of phosphatase activities and Phr peptide processing and inhibition. Additionally, we propose experiments that will provide a global view of the complex regulatory network that governs the cell's physiology through the action of the phosphatases. The widespread presence of Rap and Spo0E phosphatases among Gram-positive bacilli will allow our findings to be extrapolated to poorly understood pathogenic species, for which a better knowledge of basic physiological mechanisms seems to be an urgent need. Genetic and biochemical approaches are proposed with the aim of identifying the enzyme(s) involved in Phr peptide processing. The kinetic parameters of RapA interaction with its inhibitor PhrA and its substrate Spo0F-P will be investigated by biochemical means that will allow us to define the mechanism of pentapeptide inhibition. The proteins of the Spo0E family of phosphatases will be biochemically characterized and the genetic and physiological factors controlling their genes' transcription investigated. The role of the Rap phosphatases not involved in sporulation will be investigated by microbiological and genetic approaches

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM055594-09
Application #
7001263
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Ikeda, Richard A
Project Start
1998-01-01
Project End
2007-12-31
Budget Start
2006-01-01
Budget End
2007-12-31
Support Year
9
Fiscal Year
2006
Total Cost
$412,401
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Diaz, Alejandra R; Core, Leighton J; Jiang, Min et al. (2012) Bacillus subtilis RapA phosphatase domain interaction with its substrate, phosphorylated Spo0F, and its inhibitor, the PhrA peptide. J Bacteriol 194:1378-88
Hobbs, Carey A; Bobay, Benjamin G; Thompson, Richele J et al. (2010) NMR solution structure and DNA-binding model of the DNA-binding domain of competence protein A. J Mol Biol 398:248-63
Lehmann, Mandy; Noack, Deborah; Wood, Malcolm et al. (2009) Lung epithelial injury by B. anthracis lethal toxin is caused by MKK-dependent loss of cytoskeletal integrity. PLoS One 4:e4755
Perego, Marta; Hoch, James A (2008) Commingling regulatory systems following acquisition of virulence plasmids by Bacillus anthracis. Trends Microbiol 16:215-21
Diaz, Alejandra R; Stephenson, Sophie; Green, J Michael et al. (2008) Functional role for a conserved aspartate in the Spo0E signature motif involved in the dephosphorylation of the Bacillus subtilis sporulation regulator Spo0A. J Biol Chem 283:2962-72
Wilson, Adam C; Soyer, Magali; Hoch, James A et al. (2008) The bicarbonate transporter is essential for Bacillus anthracis lethality. PLoS Pathog 4:e1000210
Fukushima, Tatsuya; Szurmant, Hendrik; Kim, Eun-Ja et al. (2008) A sensor histidine kinase co-ordinates cell wall architecture with cell division in Bacillus subtilis. Mol Microbiol 69:621-32
Bongiorni, Cristina; Fukushima, Tatsuya; Wilson, Adam C et al. (2008) Dual promoters control expression of the Bacillus anthracis virulence factor AtxA. J Bacteriol 190:6483-92
Wilson, Adam C; Perego, Marta; Hoch, James A (2007) New transposon delivery plasmids for insertional mutagenesis in Bacillus anthracis. J Microbiol Methods 71:332-5
Kao, Mou-Chieh; Di Bernardo, Salvatore; Perego, Marta et al. (2004) Functional roles of four conserved charged residues in the membrane domain subunit NuoA of the proton-translocating NADH-quinone oxidoreductase from Escherichia coli. J Biol Chem 279:32360-6