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In vitro assessment of selenium bioavailability from selenized lactic acid bacteria using a static INFOGEST digestion model and intestinal permeability model

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F25%3A43931434" target="_blank" >RIV/60461373:22340/25:43931434 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/60460709:41210/25:102118 RIV/26722861:_____/25:N0000002

  • Výsledek na webu

    <a href="https://doi.org/10.1016/j.jtemb.2025.127632" target="_blank" >https://doi.org/10.1016/j.jtemb.2025.127632</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jtemb.2025.127632" target="_blank" >10.1016/j.jtemb.2025.127632</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    In vitro assessment of selenium bioavailability from selenized lactic acid bacteria using a static INFOGEST digestion model and intestinal permeability model

  • Popis výsledku v původním jazyce

    Background and objective: Microbial selenium (Se) supplementation is an essential area of biotechnologicalresearch due to differences in the bioavailability and toxicity of different forms of selenium. To date, research hasfocused mainly on the use of selenized yeast. However, in recent years, scientific interest has also increased inother microorganisms, such as lactic acid bacteria (LAB), which have several unique properties that can affect thequality and bioavailability of selenium. LAB, unlike yeast, can also act as probiotics, which may bring additionalhealth benefits related to improving the intestinal microbiota and supporting the health of the gastrointestinaltract.Methods: This study investigates the in vitro bioaccessibility and bioavailability of Se from two lactic acid bacterialstrains, Streptococcus thermophilus CCDM 144 and Enterococcus faecium CCDM 922 A. We evaluated Seaccumulation, speciation, and stability during simulated gastrointestinal digestion and Se permeation through aCaco-2 cell monolayer model.Results: Both strains accumulated Se, metabolizing it predominantly into selenium nanoparticles (SeNPs,64–77 % of total Se), with only a minor fraction (&lt;5 % of total Se) of organic Se species. Experiments revealedthat while organic Se species had high bioavailability (up to 90 %), their bioaccessibility during digestion wasvery low (&lt;0.1 % of total Se). In contrast, SeNPs showed high bioaccessibility (~90 %) and moderate transportefficiency through the intestinal model (16–19 % after 4 hours).Conclusion: These results highlight the potential of SeNPs produced by lactic acid bacteria as a bioaccessible formof Se for dietary supplementation. Further research is required to explore the behavior of SeNPs within thehuman body to fully understand how they can be used safely and effectively in nutrition or other applications.

  • Název v anglickém jazyce

    In vitro assessment of selenium bioavailability from selenized lactic acid bacteria using a static INFOGEST digestion model and intestinal permeability model

  • Popis výsledku anglicky

    Background and objective: Microbial selenium (Se) supplementation is an essential area of biotechnologicalresearch due to differences in the bioavailability and toxicity of different forms of selenium. To date, research hasfocused mainly on the use of selenized yeast. However, in recent years, scientific interest has also increased inother microorganisms, such as lactic acid bacteria (LAB), which have several unique properties that can affect thequality and bioavailability of selenium. LAB, unlike yeast, can also act as probiotics, which may bring additionalhealth benefits related to improving the intestinal microbiota and supporting the health of the gastrointestinaltract.Methods: This study investigates the in vitro bioaccessibility and bioavailability of Se from two lactic acid bacterialstrains, Streptococcus thermophilus CCDM 144 and Enterococcus faecium CCDM 922 A. We evaluated Seaccumulation, speciation, and stability during simulated gastrointestinal digestion and Se permeation through aCaco-2 cell monolayer model.Results: Both strains accumulated Se, metabolizing it predominantly into selenium nanoparticles (SeNPs,64–77 % of total Se), with only a minor fraction (&lt;5 % of total Se) of organic Se species. Experiments revealedthat while organic Se species had high bioavailability (up to 90 %), their bioaccessibility during digestion wasvery low (&lt;0.1 % of total Se). In contrast, SeNPs showed high bioaccessibility (~90 %) and moderate transportefficiency through the intestinal model (16–19 % after 4 hours).Conclusion: These results highlight the potential of SeNPs produced by lactic acid bacteria as a bioaccessible formof Se for dietary supplementation. Further research is required to explore the behavior of SeNPs within thehuman body to fully understand how they can be used safely and effectively in nutrition or other applications.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10608 - Biochemistry and molecular biology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/QK22010186" target="_blank" >QK22010186: Postbiotika, bakteriální exopolysacharidy a nové oligosacharidy pro funkční synbiotické fermentované výrobky</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY

  • ISSN

    0946-672X

  • e-ISSN

    1878-3252

  • Svazek periodika

    88

  • Číslo periodika v rámci svazku

    April 2025

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    9

  • Strana od-do

    nestránkováno

  • Kód UT WoS článku

    001445514400001

  • EID výsledku v databázi Scopus

    2-s2.0-86000367372