Fig. 1
source and then inoculated into fresh MM supplemented with 10 mM Mn2+, 1% DMF, 0.02 mΜ Forskolin, or 5 mM dbcAMP with 1% Avicel as the carbon source. Cultures with no added compounds were used as controls. Intracellular cAMP concentration was detected as described in the Materials and Methods. Values are the mean ± SD of the results from three independent experiments. Asterisks indicate significant differences from the control (*p < 0.05, Student’s t-test)
Intracellular cAMP concentration in T. reesei QM6a, Δacy1 and Δplc-e strains under different conditions. The QM6a, Δacy1, and Δplc-e strains were cultured in MM with 2% glucose as a carbon