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 |
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).
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.
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.