Synthesis of a number of bacterial proteins including glutamine synthetase, amino acid transport components and degradative enzymes, and nitrogenase is increased under nitrogen limiting conditions. In enteric bacteria increased synthesis appears to be mediated by products of nitrogen regulatory genes ntrA, ntrB, and ntrC, which activate transcription. Our major goals are to determine functions of the individual ntr products in regulating transcription and to identify sites to which they bind within the promoter-operator for glnA, the structural gene encoding glutamine synthetase. We will attempt to demonstrate regulatory effects of ntr products on glnA expression in vitro.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM021307-12
Application #
3270386
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1977-06-01
Project End
1988-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
12
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Wong, P K; Popham, D; Keener, J et al. (1987) In vitro transcription of the nitrogen fixation regulatory operon nifLA of Klebsiella pneumoniae. J Bacteriol 169:2876-80
Kustu, S; Hirschman, J; Meeks, J C (1985) Adenylylation of bacterial glutamine synthetase: physiological significance. Curr Top Cell Regul 27:201-13
Hirschman, J; Wong, P K; Sei, K et al. (1985) Products of nitrogen regulatory genes ntrA and ntrC of enteric bacteria activate glnA transcription in vitro: evidence that the ntrA product is a sigma factor. Proc Natl Acad Sci U S A 82:7525-9