The detoxification of ammonia in humans occurs primarily in the liver through the combined action of five enzymes. These enzymes catalyze the transformation of ammonia into urea for eventual disposition via the urine. The primary objective of this proposal is to elucidate the detailed mechanisms of action for argininosuccinate lyase and argininosuccinate synthetase. These enzymes catalyze the reactions that are currently thought to control the rate limiting steps in the metabolism of ammonia into urea. This research should have a significant impact in revealing the factors that control arginine and urea biosynthesis. This information is vital for the effective treatment of urea cycle diseases such as citrullinemia and argininosuccinate aciduria. Steadystate and rapid reaction kinetic studies along with magnetic resonance techniques will be the principle methods used in accomplishing these objectives. The primary aims of the proposed research are as follows. 1. Determine the identity of any intermediates involved in the reactions catalyzed by argininosuccinate synthetase and argininosuccinate lyase. 2. Quantitate all of the rate constants leading to the formation and breakdown of enzyme complexes occuring along the reaction pathways. 3. Identify the structural and functional roles of the divalent cations required in the argininosuccinate synthetase reaction. 4. Elucidate the amino acid at the active sites of these enzymes and determine the function of these groups in catalysis and/or binding of substrates and products.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Modified Research Career Development Award (K04)
Project #
5K04DK001366-02
Application #
3072375
Study Section
Biochemistry Study Section (BIO)
Project Start
1985-01-01
Project End
1989-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Type
Schools of Arts and Sciences
DUNS #
City
College Station
State
TX
Country
United States
Zip Code
77845
Miran, S G; Chang, S H; Raushel, F M (1991) Role of the four conserved histidine residues in the amidotransferase domain of carbamoyl phosphate synthetase. Biochemistry 30:7901-7
Caldwell, S R; Raushel, F M (1991) Detoxification of organophosphate pesticides using a nylon based immobilized phosphotriesterase from Pseudomonas diminuta. Appl Biochem Biotechnol 31:59-73
Dumas, D P; Wild, J R; Raushel, F M (1990) Expression of Pseudomonas phosphotriesterase activity in the fall armyworm confers resistance to insecticides. Experientia 46:729-31
Dumas, D P; Raushel, F M (1990) Chemical and kinetic evidence for an essential histidine in the phosphotriesterase from Pseudomonas diminuta. J Biol Chem 265:21498-503
Dumas, D P; Durst, H D; Landis, W G et al. (1990) Inactivation of organophosphorus nerve agents by the phosphotriesterase from Pseudomonas diminuta. Arch Biochem Biophys 277:155-9
Mullins, L S; Zawadzke, L E; Walsh, C T et al. (1990) Kinetic evidence for the formation of D-alanyl phosphate in the mechanism of D-alanyl-D-alanine ligase. J Biol Chem 265:8993-8
Post, L E; Post, D J; Raushel, F M (1990) Dissection of the functional domains of Escherichia coli carbamoyl phosphate synthetase by site-directed mutagenesis. J Biol Chem 265:7742-7
Donarski, W J; Dumas, D P; Heitmeyer, D P et al. (1989) Structure-activity relationships in the hydrolysis of substrates by the phosphotriesterase from Pseudomonas diminuta. Biochemistry 28:4650-5
Dumas, D P; Caldwell, S R; Wild, J R et al. (1989) Purification and properties of the phosphotriesterase from Pseudomonas diminuta. J Biol Chem 264:19659-65
Kim, S C; Raushel, F M (1988) Mechanism-based inactivation of rabbit muscle phosphoglucomutase by nojirimycin 6-phosphate. Biochemistry 27:7328-32

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