Bacteriocins: Curial guardians of gastrointestinal tract.

The human gastrointestinal (GI) tract microbiome secretes various metabolites that play pivotal roles in maintaining host physiological balance and influencing disease progression. Among these metabolites, bacteriocins-small, heat-stable peptides synthesized by ribosomes-are notably prevalent in the GI region. Their multifaceted benefits have garnered significant interest in the scientific community. This review comprehensively explores the methods for mining bacteriocins (traditional separation and purification, bioinformatics, and artificial intelligence), their effects on the stomach and intestines, and their complex bioactive mechanisms. These mechanisms include flora regulation, biological barrier restoration, and intervention in epithelial cell pathways. By detailing each well-documented bacteriocin, we reveal the diverse ways in which bacteriocins interact with the GI environment. Moreover, the future research direction is prospected. By further studying the function and interaction of intestinal bacteriocins, we can discover new pharmacological targets and develop drugs targeting intestinal bacteriocins to regulate and improve human health. It provides innovative ideas and infinite possibilities for further exploration, development, and utilization of bacteriocins. The inevitable fact is that the continuously exploration of bacteriocins is sure to bring the promising future for demic GI health understanding and interference strategy.

Optimization of the polysaccharide hydrolysate from Auricularia auricula with antioxidant activity by response surface methodology.

An efficient acid-hydrolysis method was developed and optimized for the hydrolyses of polysaccharide from Auricularia auricula with the ABTS· scavenging ability as the detective marker. Based on the single factor experimental results, Box-Behnken design (BBD) were applied for the optimization of acid-hydrolysis conditions. The possible antioxidant mechanism of the hydrolyses (AAPs-F) in vivo was performed using the C. elegans model. The acid-hydrolysis conditions were found to be the optimal hydrolyzing time 2.78h (166.8min), hydrolyzing temperature 95.04°C and the acid concentration 14.03mol/L, respectively. Under the optimal acid-hydrolysis conditions, the ABTS· scavenging ability of AAPs-H was 97.94±0.87%, which was well matched with the predicted value (99.77%) of the BBD model. AAPs-F was the main fraction of AAPs-H separated through Sephadex G-10 as the stationary phase. AAPs-F was a kind of heteropolysaccharide and comprised of glucose, galactose and fucose with the molar ratio of 50:1:2. The molecular weight of AAPs-F was 143.15kDa. AAPs-F showed a remarkable protective effect to the injury induced by hydrogen peroxide or paraquat (p<0.01), and it could up-regulate stress-resistance related enzymes including superoxide dismutase (SOD) by 109.74% and CAT by 106.84% at concentration of 0.2mg/mL in C. elegans.