microbiology, Vol 141, 1101-1108, Copyright © 1995 by Society for General Microbiology

ARTICLES

Nitrogen-regulated transcription and enzyme activities in continuous cultures of Saccharomyces cerevisiae [published erratum appears in Microbiology 1995 Aug;141(Pt 8):2019]

EG ter Schure, HH Sillje, LJ Raeven, J Boonstra, AJ Verkleij and CT Verrips
Department of Molecular Cell Biology, Utrecht University, The Netherlands.

Variations in the transcription of nitrogen-regulated genes and in the activities of nitrogen-regulated enzymes of the yeast Saccharomyces cerevisiae were studied by changing the carbon and nitrogen fluxes. S. cerevisiae was grown in continuous culture at various dilution rates (D) under nitrogen limitation with NH4Cl as sole nitrogen source. With an increase in D from 0.05 to 0.29 h-1, both the glucose and the ammonia flux increased sixfold. The activities of the two ammonia- incorporating enzymes, NADPH-dependent glutamate dehydrogenase (NADPH- GDH) and glutamine synthetase (GS), encoded by GDH1 and GLN1, respectively, increased with increasing D, while the activity of the glutamate-degrading enzyme, NAD-dependent glutamate dehydrogenase (NAD- GDH), decreased. Surprisingly, no changes were observed in the transcription of GDH1 and GLN1; however increased D was accompanied by an increase in GAP1 transcription. At the metabolite level, the increase in the glucose and nitrogen flux did not result in changes in the intracellular 2-oxoglutarate, glutamate or glutamine concentrations. It is shown that growth on ammonia alone is not sufficient to cause repression of GAP1 and GLN1 transcription and that the regulation of GAP1 transcription and both NADPH-GDH and GS activity is not an on/off switch, but is gradually modulated in correlation with the ammonia concentration.

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