Jiang, Yuan; Liu, Xiao-Chen; Ahrne, Lilia M.; Skibsted, Leif H. published the artcile< Enthalpy-entropy compensation in calcium binding to acid-base forms of glycine tyrosine dipeptides from hydrolysis of α-lactalbumin>, Synthetic Route of 112-63-0, the main research area is alpha lactalbumin hydrolysis calcium binding glycine tyrosine dipeptide; Calcium binding; Calcium bioavailability; Density Functional Theory; Dipeptide; Enthalpy–entropy compensation.
Calcium binding to peptides formed by hydrolysis of whey proteins during digestion is important for calcium uptake in the intestines and affects the antioxidant function of the peptides. For the two dipeptides, Gly-Tyr and Tyr-Gly, potential hydrolysis products of α-lactalbumin, calcium binding to the three forms of each dipeptide in acid-base equilibrium at intestinal pH was determined electrochem. and compared to binding to tyrosine for aqueous 0.16 M NaCl for 5 < pH < 9 at 15°C, 25°C, and 37°C. At milk pH at 25°C, binding of calcium to the zwitterion of GlyTyr dominates, with an association constant Kass2 = 22 M-1 with ΔH0 = -46 kJ·mol-1, while binding to the mononeg. TyrGly dominates for TyrGly with Kass3 = 32 M-1 and ΔH0 = -38 kJ·mol-1. At intestinal conditions, pH = 7 and 37°C, binding of calcium has similar affinity for GlyTyr and TyrGly, while at higher pH and lower temperature, GlyTyr binds stronger. D. Functional Theory calculations confirmed a stronger binding to the zwitterion of GlyTyr than of TyrGly and an increasing affinity with increasing pH for both. Calcium binding to the acid/base forms of the dipeptides is at neutral pH strongly exothermic with ΔH0 becoming less neg. at higher pH, and a linear enthalpy-entropy compensation (r2 = 0.99) results in comparable binding important for calcium bioavailability along the changing distribution among acid-base forms. Calcium binding decreases radical scavenging rate and antioxidative activity of both dipeptides. Food Research International published new progress about Amino acids Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Synthetic Route of 112-63-0.
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