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. 1998 Apr;180(7):1973–1977. doi: 10.1128/jb.180.7.1973-1977.1998

TABLE 1.

Effect of nmrA deletions on nitrogen metabolite repression of amdS::lacZ expression

Nitrogen sourcea β-Galactosidase level (Miller units/min/mg of protein)b
nmrA % Dere- pressionc ΔnmrA::bleoR % Dere- pressionc
Ala 12.2 ± 1.3 13.7 ± 1.5
NH4 1.8 ± 0.4 15 4.6 ± 1.5 34
Gln 2.4 ± 0.2 20 6.3 ± 0.8 46
Ala + GABA 91.2 ± 7.3 147.4 ± 16.0
Ala + GABA + NH4 6.6 ± 1.5 7 48.2 ± 10.1 33
a

Mycelium was grown for 16 h at 37°C in glucose minimal medium (9) containing in each case the following nitrogen sources: 10 mM l-alanine (Ala), 10 mM ammonium tartrate (NH4), 10 mM l-glutamine (Gln), and 10 mM γ-amino-butyric acid (GABA). 

b

β-Galactosidase levels encoded by an amdS::lacZ translational fusion gene integrated by gene replacement at the amdS locus were assayed by the method of Davis et al. (11) and are expressed as means ± standard errors. 

c

The percentage of derepression is calculated as the level of enzyme activity under repressed conditions relative to that under nonrepressed conditions: NH4 and Gln relative to the limiting nitrogen source Ala, Ala plus GABA plus NH4 relative to Ala plus GABA.