Glutamine metabolism and cycling in Neurospora crassa
Author(s) -
Jaime Mora
Publication year - 1990
Publication title -
microbiological reviews
Language(s) - English
Resource type - Journals
eISSN - 1070-6275
pISSN - 0146-0749
DOI - 10.1128/mr.54.3.293-304.1990
Subject(s) - glutamine , glutamate synthase , glutamate dehydrogenase , glutamine synthetase , biochemistry , neurospora crassa , biology , catabolism , amidase , glutamate receptor , metabolism , amino acid , enzyme , receptor , gene , mutant
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.
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