4.7 Article

Variation in the rate and extent of starch digestion is not determined by the starch structural features of cooked whole pulses

Journal

FOOD HYDROCOLLOIDS
Volume 83, Issue -, Pages 340-347

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2018.05.022

Keywords

Cell walls; In vitro starch digestion kinetics; Pulse; Structural features

Funding

  1. National Natural Science Foundation of China [31701546]
  2. Natural Science Foundation of Guangdong Province [2017A030313207]
  3. National Key Research and Development Program of China [2017YFD0400502]
  4. Science and Technology Planning Project of Nansha, Guangzhou [2016GJ001]
  5. Fundamental Research Funds for the Central Universities of China [2017MS100]
  6. 111 Project [B17018]

Ask authors/readers for more resources

Cooked whole pulses are widely accepted as a low glycemic food with potential health benefits of reducing the risk of obesity and type 2 diabetes. However, the structural basis for the variation in digestion rate and extent of different pulses is still unclear. In this study, intact cotyledon cells of four commercial pulses (i.e., pinto bean, garbanzo bean, green-split pea, and black-eyed pea) were isolated under controlled cooking and isolation conditions, as a model for whole foods. We investigated the macrostructure of intact cells and structural features of entrapped starch granules, such as crystallinity and thermal parameters, and diffusion of an amylase-sized FITC dextran probe into intact cells. In vitro digestion kinetic profiles of pulse cells were monitored by a reducing sugar assay with a fixed alpha-amylase activity, and were fitted into a first order model to obtain the apparent rate coefficient and digestion extent at 180 min. Pearson's correlation analysis suggested that there is no significant correlation between the kinetic parameters and structural features of entrapped starch granules nor the size of the cell particles. It is concluded that the starch digestibility of isolated pulses is controlled by the accessibility of digestive enzymes, which is limited by the rigid cell wall and/or pulse protein matrix, rather than starch structure.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available