Descriptors :
legume cells , stomach model , duodenum model , amylase digestion , barrier properties , non-specific binding
Abstract :
Retention of intact plant cells to the end of the small intestine leads to transport of entrapped
macronutrients such as starch and protein for colonic microbial fermentation, and is a
promising mechanism to increase the content of resistant starch in diets. However, the effect
of gastro-intestinal bio-mechanical processing on the intactness of plant cells and the
subsequent resistance to enzymatic digestion of intracellular starch and protein are not well
understood. In this study, intact cells isolated from legume cotyledons are digested in a
laboratory model which mimics the mechanical and biochemical conditions of the rat
stomach and duodenum. The resulting digesta are characterised in terms of cell (wall)
integrity as well as intracellular starch and protein hydrolysis. The cells remained essentially
intact in the model with negligible (ca 2-3%) starch or protein digestion; however when the
cells were mechanically broken and digested in the model, the hydrolysis was increased to
45-50% suggesting that intact cellular structures could survive the mixing regimes in the
model stomach and duodenum sufficiently to prevent digestive enzyme access. Apart from
intact cell walls providing effective barrier properties, they also limit digestibility by
restricting starch gelatinisation during cooking, and significant non-specific binding of α-
amylase is observed to both intact and broken cell wall components, providing a third
mechanism hindering starch hydrolysis. The study suggests that the preservation of intactness
of plant cells, such as from legumes, could be a viable approach to achieve the targeted
delivery of resistant starch to the colon.
Title of Article :
Digestion of isolated legume cells in a stomach-duodenum model: three mechanisms limit starch and protein hydrolysis
Author/Authors :
Bhattarai, Rewati R. , Dhital, Sushil , Wu, Peng , Chen, Xiao Dong , Gidley, Michael J.
Author/Authors - جزئيات :