Raising temperature from 25°C to 35°C significantly enhances starch digestion kinetics:
α-Amylase (salivary, pancreatic) Q₁₀ ≈ 1.5–2.0. 10°C rise → 1.5–2× rate increase. Optimum ~37°C; 35°C approaches peak.
Granule swelling/rupture accelerates with temperature. At 35°C, granules hydrate faster → more accessible to amylase. Full gelatinization typically >60°C, but pre-gelatinization softening occurs at 35°C.
Increased molecular motion → faster enzyme-substrate collision frequency (Arrhenius).
Colonic microbiota (if considering in vitro fermentation models) show enhanced amylolytic activity at 35°C vs 25°C.
Intestinal glucose transporters (SGLT1, GLUT2) function optimally at body temperature; 35°C improves uptake vs. 25°C.
>40°C denatures amylase; fever >39°C may transiently impair digestion.
Physiologic temperature (37°C) is evolutionary optimum for human digestive enzymes.