4.6 Article

Effect of Fermentation with Streptococcus thermophilus Strains on In Vitro Gastro-Intestinal Digestion of Whey Protein Concentrates

Journal

MICROORGANISMS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms11071742

Keywords

Streptococcus thermophilus; whey protein concentrate; bioactive peptides; peptidomics; gastro-intestinal digestion; angiotensin-converting enzyme inhibition; valine-proline-proline; isoleucine-proline-proline

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This study investigated the impact of simulated gastrointestinal digestion on whey protein concentrate (WPC) hydrolysates fermented with S. thermophilus strains. Fermentation enhanced protein hydrolysis and release of bioactive peptides, but some of the peptides could be broken down during digestion. WPC hydrolysates fermented with different strains showed varying biological activities, which were linked to the amount of bioactive peptides present.
Three Streptococcus thermophilus strains, namely RBC6, RBC20, and RBN16, were proven to release bioactive peptides during whey protein concentrate (WPC) fermentation, resulting in WPC hydrolysates with biological activities. However, these bioactive peptides can break down during gastro-intestinal digestion (GID), hindering the health-promoting effect of fermented WPC hydrolysates in vivo. In this work, the effect of simulated GID on three WPC hydrolysates fermented with S. thermophilus strains, as well as on unfermented WPC was studied in terms of protein hydrolysis, biological activities, and peptidomics profiles, respectively. In general, WPC fermentation enhanced protein hydrolysis compared to unfermented WPC. After in vitro GID, WPC fermented with S. thermophilus RBC20 showed the highest antioxidant activity, whereas WPC fermented with strain RBC06 displayed the highest angiotensin-converting enzyme (ACE)- and dipeptidyl peptidase IV (DPP-IV)-inhibitory activities. Peptidomics analysis revealed that all digested WPC samples were highly similar to each other in peptide profiles, and 85% of the 46 identified bioactive peptides were shared among fermented and unfermented samples. However, semi-quantitative analysis linked the observed differences in biological activities among the samples to differences in the amount of bioactive peptides. The anti-hypertensive peptides VPP and IPP, as well as the DPP-IV-inhibitory peptide APFPE, were quantified. In conclusion, WPC fermentation with S. thermophilus positively impacted protein hydrolysis and bioactive peptide release during GID.

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