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The bacterial pellet was then resuspended in 800 L of GMML liquid medium (M9 salts, 1% glycerol, 1 mM MgSO 4 and 0.1 mM CaCl 2 and 0.3 mM Leucine) containing Amp, Spe, IPTG (0.5 mM) and a specific ncAA (1 mM), This suspension was then transferred to 96-deep-well plates (2.2 mL) and incubated at 37 C, 220 rpm for 11 h, with monitoring of fluorescence intensity (excitation 485 nm and emission 515 nm) as well as OD 600 by Microplate Readers

Caspase-Glo reagent was added to the wells according to the manufacturers instructions and luminescent signal was measured on a SpectraMax M3 microplate reader (Molecular Devices)