The overall objective of the proposed research is to elucidate the molecular mechanism of sensory processing in E. coli and S. typhimurium chemotaxis. Sensory-motor regulation in bacteria represents a useful model system for the study of receptor- mediated control of cell behavior. Receptor activity is controlled by 2 enzymes, an S-adenosylmethionine:glutamate methytransferase and a glutamyl methylesterase. Genetic studies have identified 4 additional cytoplasmic proteins required for chemotaxis, the products of the cheA, cheW, cheY, and cheZ genes. The specific goals in this grant period include determining the structure-function relationships which underlie the activities of the receptor modification enzymes. What is the role of the regulatory domain of the esterase? Is a thioester adduct between the receptors and the esterase important in chemotaxis? What is the physiological significance of the methylation reactions in chemosensing? The biochemistry of the auxiliary signalling proteins will also be investigated. Specific projects include determining the role of CheA in the regulation of the methylesterase, determining the possible role of nucleotides in CheW function, and elucidating the mechanism and significance of CheZ methylation. The coordinate functioning of these components will be investigated using a variety of genetic approaches, including the selection of second site mutations which compensate defined lesions in critical structural features of the Che proteins. Finally, attempts will be made to extend results obtained with chemotaxis to cognate regulatory systems in bacteria including the apparatus in B. subtilis which triggers the developmental switch from vegetative growth to endospore formation, and the mechanism in E. coli which regulates porin expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI020980-07
Application #
3130865
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1984-03-01
Project End
1992-11-30
Budget Start
1990-12-01
Budget End
1991-11-30
Support Year
7
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Princeton University
Department
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Levit, Mikhail N; Abramczyk, Bozena M; Stock, Jeffry B et al. (2002) Interactions between Escherichia coli nucleoside-diphosphate kinase and DNA. J Biol Chem 277:5163-7
Alon, U; Camarena, L; Surette, M G et al. (1998) Response regulator output in bacterial chemotaxis. EMBO J 17:4238-48
Liu, Y; Levit, M; Lurz, R et al. (1997) Receptor-mediated protein kinase activation and the mechanism of transmembrane signaling in bacterial chemotaxis. EMBO J 16:7231-40
de Jonge, R; Teixeira de Mattos, M J; Stock, J B et al. (1996) Pyrroloquinoline quinone, a chemotactic attractant for Escherichia coli. J Bacteriol 178:1224-6
Zahner, D; Grebe, T; Guenzi, E et al. (1996) Resistance determinants for beta-lactam antibiotics in laboratory mutants of Streptococcus pneumoniae that are involved in genetic competence. Microb Drug Resist 2:187-91
Surette, M G; Stock, J B (1996) Role of alpha-helical coiled-coil interactions in receptor dimerization, signaling, and adaptation during bacterial chemotaxis. J Biol Chem 271:17966-73
Levit, M; Liu, Y; Surette, M et al. (1996) Active site interference and asymmetric activation in the chemotaxis protein histidine kinase CheA. J Biol Chem 271:32057-63
Surette, M G; Levit, M; Liu, Y et al. (1996) Dimerization is required for the activity of the protein histidine kinase CheA that mediates signal transduction in bacterial chemotaxis. J Biol Chem 271:939-45
Hakenbeck, R; Stock, J B (1996) Analysis of two-component signal transduction systems involved in transcriptional regulation. Methods Enzymol 273:281-300
Philips, M R; Staud, R; Pillinger, M et al. (1995) Activation-dependent carboxyl methylation of neutrophil G-protein gamma subunit. Proc Natl Acad Sci U S A 92:2283-7

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