The long-term objective of this program is to understand the mechanisms responsible for formation of the bacterial division site, and for the correlation of division site localization and septum formation with the equipartition of progeny chromosomes into the two daughter cells. To approach these objectives, we have the following specific aims for the proposed grant period. 1. To describe the developmental history of the E.coli cell division site by characterizing cell division mutants that are blocked at intermediate stages of the developmental pathway, prior to the onset of septal invagination. 2. To identify proteins that are associated with periseptal annuli and other zones of adhesion by using chemical crosslinking and immunolocalization methods. 3. To identify the membrane components that are responsible for the specific binding of oriC to the cell envelope, and to define the relation of chromosome replication and segregation to the genesis and localization of new division sites. 4. To determine whether the residual division sites that are present at the cell poles play a role in the generation of future division sites within the cell.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053276-18
Application #
6519683
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Deatherage, James F
Project Start
1985-03-01
Project End
2004-03-31
Budget Start
2002-04-01
Budget End
2004-03-31
Support Year
18
Fiscal Year
2002
Total Cost
$256,872
Indirect Cost
Name
University of Connecticut
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
Shih, Yu-Ling; Le, Trung; Rothfield, Lawrence (2003) Division site selection in Escherichia coli involves dynamic redistribution of Min proteins within coiled structures that extend between the two cell poles. Proc Natl Acad Sci U S A 100:7865-70
Fu, X; Shih, Y L; Zhang, Y et al. (2001) The MinE ring required for proper placement of the division site is a mobile structure that changes its cellular location during the Escherichia coli division cycle. Proc Natl Acad Sci U S A 98:980-5
Justice, S S; Garcia-Lara, J; Rothfield, L I (2000) Cell division inhibitors SulA and MinC/MinD block septum formation at different steps in the assembly of the Escherichia coli division machinery. Mol Microbiol 37:410-23
Rowland, S L; Fu, X; Sayed, M A et al. (2000) Membrane redistribution of the Escherichia coli MinD protein induced by MinE. J Bacteriol 182:613-9
Hale, C A; de Boer, P A (1999) Recruitment of ZipA to the septal ring of Escherichia coli is dependent on FtsZ and independent of FtsA. J Bacteriol 181:167-76
Cook, W R; Rothfield, L I (1999) Nucleoid-independent identification of cell division sites in Escherichia coli. J Bacteriol 181:1900-5
King, G F; Pan, B; Maciejewski, M W et al. (1999) Backbone and side-chain 1H, 15N, and 13C assignments for the topological specificity domain of the MinE cell division protein. J Biomol NMR 13:395-6
Shakibai, N; Ishidate, K; Reshetnyak, E et al. (1998) High-affinity binding of hemimethylated oriC by Escherichia coli membranes is mediated by a multiprotein system that includes SeqA and a newly identified factor, SeqB. Proc Natl Acad Sci U S A 95:11117-21
Ishidate, K; Ursinus, A; Holtje, J V et al. (1998) Analysis of the length distribution of murein glycan strands in ftsZ and ftsI mutants of E. coli. FEMS Microbiol Lett 168:71-5
Garcia-Lara, J; Shang, L H; Rothfield, L I (1996) An extracellular factor regulates expression of sdiA, a transcriptional activator of cell division genes in Escherichia coli. J Bacteriol 178:2742-8