Stimulatory effect of arginine on acetylglutamate synthesis in isolated mitochondria of mouse and rat liver
- 1 December 1985
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 232 (2) , 329-334
- https://doi.org/10.1042/bj2320329
Abstract
N-Acetyl-L-glutamate synthetase (EC 2.3.1.1) catalyses the synthesis of N-acetyl-L-glutamate, an allosteric activator of carbamoyl-phosphate synthetase I in the liver of ureotelic animals, and the first enzyme is activated specifically by arginine. We have proposed that arginine can stimulate acetylglutamine synthetase in vivo and thereby release the mitochondrial content of acetylglutamate. The effects of arginine on acetylglutamate synthesis in isolated mitochondria were investigated in detail in the present work. (1) When rat liver mitochondria were isolated and incubated with [14C]glutamate and unlabeled acetate as substrates, acetyl[14C]glutamate synthesis in the mitochondria was more extensive in the presence than in the absence of L-arginine. There was no significant difference between the specific radioactivities of intramitochondrial [14C]glutamate in the presence and absence of arginine. (2) When rat liver mitochondria were incubated with [14C]acetate and unlabeled glutamate as substrates, arginine also stimulated acetyl[14C]glutamate synthesis in the isolated mitochondria. (3) L-Lysine orL-homoarginine, which does not acivate acetylglutamate synthetase, had no effect on acetylglutamate synthesis, in the isolated mitochondria. (4) The arginine concentration giving half-maximal synthesis of acetylglutamate in isolated mitochondria was about 50 .mu.M, which is in the range of physiological concentrations of arginine in the liver. (5) As we previously reported [Kawamoto, Ishida, Mori and Tatibana (1982) Eur. J. Biochem. 123. 637-641], the sensitivity of acetylglutamate synthetase to arginine activation undergoes marked changes after food ingestion. The extent of arginine activation of acetylglutamate synthesis in isolated mitochondria correlated well with the sensitivity of acetylglutamate synthetase extracted from the mitochondria to arginine activation. (6) These data lend further support to the idea that arginine itself activates the mitochondrial synthesis of acetylglutamate.This publication has 30 references indexed in Scilit:
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