The arylesterase activity of recombinant PON1 was measured either in the absence or presence of currant extract at various concentrations (1–10 μg GAE/mL). As the enzyme source, we used 50 µL of cell medium of HEK293 cells transfected, in a 12-well plate, with the pcDNA3.1+/C-(K)-DYK/PON1 vector and cultured in the absence of currant extract, as described above. The arylesterase activity of recombinant PON1 was determined by monitoring the increase in absorbance, following phenyl acetate hydrolysis, at 270 nm for 10 min.
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