The FAST method is based on the determination of maximal fluorescence emiss
ion when exciting at 330-350 nm, which corresponds to molecular structures
formed between reducing sugars or oxidizing lipids and lysine residues bf p
roteins. This fluorescence is dependent on heat treatment and related to pr
otein nutritional loss. Applied to a soluble extract of the food and correc
ted for the protein concentration of the solution obtained, using Trp fluor
escence, the method allows to calculate the FAST index (FI), an indicator o
f the nutritional damage during heat process. The method, firstly validated
on milk samples, is demonstrated here to well correlate with lysine damage
on various food products, such as heat-treated milk and breakfast cereals,
essentially modified hy the Maillard reaction, and roasted soybean or cook
ed salmon, where interactions between oxidizing lipids and proteins better
take place.
Independently on the food product or the type of hear process, the FAST ind
ex appears always well correlated (r(2): 0.84-0.98) to the lysine loss, the
latter being estimated by determination of acid-released lysine, fluoresca
mine-reactive lysine or infrared. Shortly, roasted corn flakes appeared to
be more damaged than extrudated flour (FI 100 and lysine blockage 40% inste
ad of 55 and 30%), condensed milk more than UHT milk (FI 150 and 85% of aci
d-released lysine instead of 80 and 94%), and steam-cooked salmon much less
than pan-fried (FI 28 instead of 372). Roasted soy can reach FI of more th
an 300 corresponding to chemical lysine loss of 40% and poultry-digestive l
ysine loss of 100%. As a conclusion, the FAST method, once precisely calibr
ated with pertinent nutritional indicators, should be of great interest for
controlling or adapting a process in order to ensure a better nutritional
quality for the food product.