Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1990 Sep;54(3):293-304.
doi: 10.1128/mr.54.3.293-304.1990.

Glutamine metabolism and cycling in Neurospora crassa

Affiliations
Review

Glutamine metabolism and cycling in Neurospora crassa

J Mora. Microbiol Rev. 1990 Sep.

Abstract

Evidence for the existence of a glutamine cycle in Neurospora crassa is reviewed. Through this cycle glutamine is converted into glutamate by glutamate synthase and catabolized by the glutamine transaminase-omega-amidase pathway, the products of which (2-oxoglutarate and ammonium) are the substrates for glutamate dehydrogenase-NADPH, which synthesizes glutamate. In the final step ammonium is assimilated into glutamine by the action of a glutamine synthetase (GS), which is formed by two distinct polypeptides, one catalytically very active (GS beta), and the other (GS alpha) less active but endowed with the capacity to modulate the activity of GS alpha. Glutamate synthase uses the amide nitrogen of glutamine to synthesize glutamate; glutamate dehydrogenase uses ammonium, and both are required to maintain the level of glutamate. The energy expended in the synthesis of glutamine drives the cycle. The glutamine cycle is not futile, because it is necessary to drive an effective carbon flow to support growth; in addition, it facilitates the allocation of nitrogen or carbon according to cellular demands. The glutamine cycle which dissipates energy links catabolism and anabolism and, in doing so, buffers variations in the nutrient supply and drives energy generation and carbon flow for optimal cell function.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Bacteriol. 1988 Sep;170(9):3961-6 - PubMed
    1. J Bacteriol. 1982 Apr;150(1):105-12 - PubMed
    1. Biochem Biophys Res Commun. 1980 Jan 15;92(1):127-33 - PubMed
    1. J Biol Chem. 1976 Aug 10;251(15):4787-91 - PubMed
    1. J Biol Chem. 1984 Jul 25;259(14):8875-9 - PubMed

Publication types

MeSH terms

LinkOut - more resources