Available lysine and fluorescence in heated milk proteins/dextrinomaltose or lactose solutions

In order to predict and compare the effects of dextrinomaltose and lactose on available lysine loss by the Maillard reaction, six model systems were prepared by mixing casein, laboratory whey protein or commercial whey protein with dextrinomaltose or lactose. The solutions were prepared at concentrations similar to those used in enteral and infant formula processing and were heated at 100, 120 or 140 °C for 0–30 min. The progress of the Maillard reaction in these model systems was followed by monitoring free fluorescence intermediary compounds. Model systems with lactose showed higher available lysine less than the model systems with dextrinomaltose; linear lysine losses were obtained between 0 and 20 min at 100 and 120 °C. At sterilization temperature and time (120 °C/10 min), lysine losses of milk proteins with dextrinomaltose as reducing sugar were 6.1% for casein, 4.1% for laboratory whey protein and 13.4% for commercial whey protein. Available lysine showed correlation with furosine in model systems prepared with lactose and casein or laboratory but not commercial whey protein at 100 and 120 °C. The initial fluorescence value obtained by mixing casein or laboratory whey protein with lactose or dextrinomaltose was low (between 3.8 and 5.7), whereas the value obtained when commercial whey proteins were used was close to 9. At 120 °C/10 min, there was only a small increase of fluorescence in casein and laboratory whey protein but a large increase in commercial whey protein (threefold the initial value). Fluorescence measurement is useful for finding the extent of the Maillard reaction in commercial whey protein (thermally damaged protein). An absolute value greater than 10 may indicate that products were prepared with thermally damaged proteins.