Protein Purification and Characterization from Bacterial Strains
The strains and plasmids used in this study were listed in Table 2. Bacillus subtilis 168 and E. coli were grown on Luria-Bertani (LB) medium. When needed, antibiotics were added to the medium at the following concentrations: ampicillin, 100 μg/ml; kanamycin, 50 μg/ml. All media were sterilized by autoclaving at 121 °C for 20 min.
The antibodies and columns for purification of proteins used were as follows: anti-acetyl-lysine antibody (ImmuneChem Pharmaceuticals, Burnaby, CA); pan anti-propionyl-lysine antibody (PTM Biolabs); HRP conjugates (anti-PrK; ImmuneChem); glutathione transferase (GST) agarose column and nickel-nitrilotriacetic acid (Ni-NTA) superflow column (Qiangen, Valencia, CA).
Wang M.M., You D, & Ye B.C. (2017). Site-specific and kinetic characterization of enzymatic and nonenzymatic protein acetylation in bacteria. Scientific Reports, 7, 14790.
Autoclaving at 121 °C for 20 min to sterilize all media
controls
Positive control: Not explicitly mentioned
Negative control: Not explicitly mentioned
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