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Intragastric Gelation of Heated Soy Protein Isolate‐Alginate Mixtures and Its Effect on Sucrose Release
Author(s) -
Huang Zhaozhi,
Gruen Ingolf,
Vardhanabhuti Bongkosh
Publication year - 2018
Publication title -
journal of food science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 150
eISSN - 1750-3841
pISSN - 0022-1147
DOI - 10.1111/1750-3841.14192
Subject(s) - sucrose , chemistry , digestion (alchemy) , gastric fluid , soy protein , food science , chromatography , rheology , zeta potential , particle size , postprandial , polysaccharide , apparent viscosity , biochemistry , chemical engineering , materials science , insulin , microbiology and biotechnology , nanoparticle , engineering , composite material , biology
The goal of our study was to investigate the effect of alginate on in vitro gastric digestion and sucrose release of soy protein isolate (SPI) in model beverages. Model beverages containing 5% w/w SPI, 0% to 0.20% w/w alginate, and 10% w/w sucrose were prepared by heating the mixtures at 85 °C for 30 min at pH 6.0 or 7.0. Characterizations of beverages included determination of zeta potential, particle size and rheological properties. Digestion patterns and sucrose release profiles were determined during 2 hr in vitro gastric digestion using SDS‐PAGE and HPLC analysis, respectively. Increasing alginate concentration led to increased negative surface charge, particle size, as well as viscosity and pseudoplastic behavior; however, no phase separation was observed. SPI beverages formed intragastric gel during in vitro gastric digestion when the formulations contained alginate or at pH 6.0 without alginate. Formation of the intragastric gel led to delayed protein digestion and release of sucrose. Higher resistance to digestion and a slower sucrose release rate were exhibited at increased alginate concentration, and to a lesser extent, at pH 6.0. This suggests that electrostatic interaction between SPI and alginate that occurred when the beverages were under gastric condition could be responsible for the intragastric gelation. These results could potentially lead to the formulation of SPI beverages with functionality to lower postprandial glycemic response. Practical Application The results could be used to design beverages or semi solid food products with altered digestion properties and lowered or slower glucose release.