Kidney and other tissues of animals and humans have a high
concentration of citrate which is an important intermediate substance
in the citrate cycle. Citrate may play an important physiological role
in metabolism. In this paper, we studied the interaction of the sodium
salt of citrate with aminoacylase which is an important enzyme in
metabolism and found sodium citrate can enhance the activity of
aminoacylase. The maximum enzyme activity induced by sodium citrate
increased approximately 3 folds over the enzyme activity without sodium
citrate. The initial reaction rates for different concentrations of
sodium citrate were obtained, showing that sodium citrate is a
non-competitive activator. The result of the ANS binding fluorescence
measurements for aminoacylase indicated that increasing sodium citrate
concentrations markedly increased the ANS binding fluorescence with a
blue shift of the emission spectra peak. This suggests the formation of
more hydrophobic regions. Aggregates formed quickly when aminoacylase
was incubated with sodium citrate (0.3 mol/L) and guanidinium chloride
(0-3.5 mol/L). Aminoacylase lost enzyme activity in the guanidinium
chloride more quickly in the presence of sodium citrate than in the
absence of sodium citrate. The intrinsic fluorescence emission
intensity decreased more quickly and the red shift of the emission
spectra peak was larger than that without sodium citrat