Investigating casein gel structure during gastric digestion using ultra-small and small-angle neutron scattering

[Display omitted] •The first study to monitor gastric devolution of casein gels using USANS and SANS.•Gels prepared in D2O exhibit earlier onset of gelation, are firmer yet more brittle compared to H2O.•Rennet-induced gel structure is sensitive to the acidic environment of the stomach.•Pepsin induce...

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Veröffentlicht in:Journal of colloid and interface science 2021-07, Vol.594, p.561-574
Hauptverfasser: Bayrak, Meltem, Mata, Jitendra, Raynes, Jared K., Greaves, Mark, White, Jacinta, Conn, Charlotte E., Floury, Juliane, Logan, Amy
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Sprache:eng
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Zusammenfassung:[Display omitted] •The first study to monitor gastric devolution of casein gels using USANS and SANS.•Gels prepared in D2O exhibit earlier onset of gelation, are firmer yet more brittle compared to H2O.•Rennet-induced gel structure is sensitive to the acidic environment of the stomach.•Pepsin induces micelle swelling and promotes higher levels of protein digestion in the stomach.•Acidification and shear govern early gastric digestion kinetics. This study aimed to understand the structural devolution of 10% w/w rennet-induced (RG) and transglutaminase-induced acid (TG) gels in H2O and D2O under in vitro gastric conditions with and without pepsin. The real-time devolution of structure at a nano- (e.g. colloidal calcium phosphate (CCP) and micelle) and micro- (gel network) level was determined using ultra-small (USANS) and small-angle neutron scattering (SANS) with electron microscopy. Results demonstrate that gel firmness or elasticity determines disintegration behaviour during simulated mastication and consequently the particle size entering the stomach. Shear of mixing in the stomach, pH, and enzyme activity will also affect the digestion process. Our results suggest that shear of mixing primarily results in erosion at the particle surface and governs gel disintegration behaviour during the early stages of digestion. Pepsin diffusivity, and hence action, occur more readily in the latter stages of gastric digestion via access to the particle interior. This occurs via the progressively larger pores of the looser gel network and channels created within the larger, less dense casein micelles of the RG gels. Gel firmness and brittleness were greater in the D2O samples compared to H2O, facilitating gel disintegration. Despite the higher strength and elasticity of RG compared to TG, the protein network strands of the RG gels become more compact when exposed to the acidic gastric environment with comparatively larger pores observed through SEM imaging. This led to a higher degree of digestibility in RG gels compared to TG gels. This is the first study to examine casein gel structure during simulated gastric digestion using scattering and highlights the benefits of neutron scattering to monitor structural changes during digestion at multiple length scales.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2021.03.087