Cell division in the bacterium Caulobacter crescentus produces two different cell types: a motile swarmer cell and a sessile stalked cell. Only the stalked cell is capable of DNA replication and cell division. The long term goal of this project is to understand how cell division and cell differentiation are regulated and coordinated in Caulobacter. Caulobacter is particularly well suited for these studies because it undergoes a relatively simple developmental program with distnct morphologies, and because cell populations can be synchronized easily. The first objective is to define the cell cycle and developmental controls of cell division initiation through an understanding of the factors that control FtsZ. As part of this objective, Dr. Brun plans to explore the mechanism of cell type-specific proteolysis of FtsZ, determine the developmental and temporal control of FtsZ localization, and identify proteins that interact with FtsZ. The second objective is to characterize the regulatory sequences and trans-acting factors responsible for regulation of ftsQA and determine how the transcription of ftsQA is coupled to DNA replication. The final objective is to identify the sigma-54-dependent genes that are required to link pole development to cell division and to define the function of stpA, which appears to be required for proper localization of the stalk and holdfast.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM051986-07
Application #
6342902
Study Section
Special Emphasis Panel (ZRG1-MBC-2 (02))
Program Officer
Greenberg, Judith H
Project Start
1995-01-01
Project End
2003-12-31
Budget Start
2001-01-01
Budget End
2001-12-31
Support Year
7
Fiscal Year
2001
Total Cost
$249,101
Indirect Cost
Name
Indiana University Bloomington
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Bharat, Tanmay A M; Kureisaite-Ciziene, Danguole; Hardy, Gail G et al. (2017) Structure of the hexagonal surface layer on Caulobacter crescentus cells. Nat Microbiol 2:17059
Ellison, Courtney K; Kan, Jingbo; Dillard, Rebecca S et al. (2017) Obstruction of pilus retraction stimulates bacterial surface sensing. Science 358:535-538
Kuru, Erkin; Lambert, Carey; Rittichier, Jonathan et al. (2017) Fluorescent D-amino-acids reveal bi-cellular cell wall modifications important for Bdellovibrio bacteriovorus predation. Nat Microbiol 2:1648-1657
Bisson-Filho, Alexandre W; Hsu, Yen-Pang; Squyres, Georgia R et al. (2017) Treadmilling by FtsZ filaments drives peptidoglycan synthesis and bacterial cell division. Science 355:739-743
Baker, Joshua D; Kysela, David T; Zhou, Jinsheng et al. (2016) Programmable, Pneumatically Actuated Microfluidic Device with an Integrated Nanochannel Array To Track Development of Individual Bacteria. Anal Chem 88:8476-83
Kysela, David T; Randich, Amelia M; Caccamo, Paul D et al. (2016) Diversity Takes Shape: Understanding the Mechanistic and Adaptive Basis of Bacterial Morphology. PLoS Biol 14:e1002565
Pereira, Ana R; Hsin, Jen; Król, Ewa et al. (2016) FtsZ-Dependent Elongation of a Coccoid Bacterium. MBio 7:
Ducret, Adrien; Quardokus, Ellen M; Brun, Yves V (2016) MicrobeJ, a tool for high throughput bacterial cell detection and quantitative analysis. Nat Microbiol 1:16077
Liechti, George; Kuru, Erkin; Packiam, Mathanraj et al. (2016) Pathogenic Chlamydia Lack a Classical Sacculus but Synthesize a Narrow, Mid-cell Peptidoglycan Ring, Regulated by MreB, for Cell Division. PLoS Pathog 12:e1005590
Curtis, Patrick D (2016) Essential Genes Predicted in the Genome of Rubrivivax gelatinosus. J Bacteriol 198:2244-50

Showing the most recent 10 out of 88 publications