The added ammonia was assimilated immediately, and no ammonium accumulated in the medium (Figure 4C).
All the selected lines showed proliferation in WPM culture medium (Figure 1).
The growth of all strains, including P. alcaligenes DIP1, on LB complex medium (Figure 3) was very similar.
In PHB consumption medium (Figure 1C), minimal medium with no exogenous carbon, the intracellular PHB accumulated during the PHB production phase was used as a carbon source.
In Figure 6a the spiral is moving horizontally in the tissue and the dipole is fixed at 10.5 mm from the medium (Figure 1).
Cells treated with 10 100 mg/L arnica extract and 10 500 mg/L wormwood extract secreted less than 15% LDH into the culture medium (Figure 1B).
Surfactant molecules originally present in the water phase assemble into rod and wormlike micelles during the premixing of the acidic water medium (Figure 11a).
The α-amylase activity of HF-TAMY cells was highest when maltose was the C source (YPM medium, Figure 2D), indicating that gene expression was induced by maltose.
Nearly 100% of the cells had taken up Nile Red from nanoparticles compared to 37% when Nile Red was dissolved in medium (Figure 1a).
