Starvation is a common experience of bacteria in most natural environments, including the hosts of pathogens, and such bacteria have applied importance. We have found that the nondifferentiating bacterium Escherichia coli selectively expresses several temporal classes of unique proteins in the first 3-5 hours of carbon starvation. This phenomenon generates stress-resistant cells (starvation, heat, oxidative and osmotic stresses). Three classes of such genes so far identified are: the cst genes--induced only under carbon starvation and requiring cyclic AMP/CRP; the csi genes--also induced by carbon starvation alone but independent of cAMp; and the pex genes--cAMP/CRP-independent and also induced by starvation for nutrients other than carbon. The genes of the latter classes appear responsible for the development of stress resistance, but the induction of all classes may depend on transcriptional systems unique to the postexponential phase. To explore this transcriptional system, we will clone and sequence one each of cst and csi genes, and two pex genes. For cloning the promoter and promoter-proximal regions of the nonessential genes, chromosomal (bla)lacZ fusions and defective plasmid-encoded bla gene reconstitution will be used; hybridization probes derived therefrom will be used in cloning the structural genes. For the essential genes alternate approaches, such as microsequencing of proteins isolated from 2-D PAGE, will be used. Using the cloned genes, the starvation gene dosage effect on survival will be investigated. Appropriate fusions will also be used to identify cis and trans acting regulatory components of the carbon starvation regulon.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042159-02
Application #
3300703
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1989-04-01
Project End
1992-03-31
Budget Start
1990-04-01
Budget End
1991-03-31
Support Year
2
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Matin, A (1992) Physiology, molecular biology and applications of the bacterial starvation response. Soc Appl Bacteriol Symp Ser 21:49S-57S
Jenkins, D E; Auger, E A; Matin, A (1991) Role of RpoH, a heat shock regulator protein, in Escherichia coli carbon starvation protein synthesis and survival. J Bacteriol 173:1992-6
Matin, A (1991) The molecular basis of carbon-starvation-induced general resistance in Escherichia coli. Mol Microbiol 5:3-10
McCann, M P; Kidwell, J P; Matin, A (1991) The putative sigma factor KatF has a central role in development of starvation-mediated general resistance in Escherichia coli. J Bacteriol 173:4188-94
Blum, P H; Jovanovich, S B; McCann, M P et al. (1990) Cloning and in vivo and in vitro regulation of cyclic AMP-dependent carbon starvation genes from Escherichia coli. J Bacteriol 172:3813-20
Jenkins, D E; Chaisson, S A; Matin, A (1990) Starvation-induced cross protection against osmotic challenge in Escherichia coli. J Bacteriol 172:2779-81