Degradation of pectin with probiotic candidate Bacillus subtilis HA1 to oligosaccharides with enhanced anticancer and antioxidant properties
2025 (Engelska)Ingår i: International Journal of Biological Macromolecules, ISSN 0141-8130, E-ISSN 1879-0003, Vol. 331, artikel-id 148501Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Upcycling fruit waste into health-promoting ingredients is an urgent sustainability challenge. In this work, a microbial degradation is described that converts apple pectin into bioactive pectic oligosaccharides (POS) using Bacillus subtilis HA1, a strain isolated from traditional yogurt. HA1 is γ-hemolytic, lecithinase-negative, and free of nhe/hbl enterotoxin genes, yet endures acid/bile and adheres to intestinal cells, confirming its safety and probiotic aptitude. The bacterium cleaves pectin within 6 h of incubation, and under optimum conditions (50 °C, pH 6), the extracellular pectinase showed a maximum activity of ≈18 IU/mL. TLC, LC–ESI–MS, and FTIR verify the formation of low-methylated mono- to tri-galacturonic acids. Crude POS scavenge up to 90 % of DPPH radicals at 10 mg/mL, which is five-fold higher than untreated pectin. POS also act selectively against tumor cells: MCF-7 breast cancer viability drops to 17 %, while healthy L-929 and HUVEC cells remain ≥95 % viable. Flow cytometry and qRT-PCR confirm apoptosis via Bax up-regulation and galectin-3 suppression. Altogether, probiotic candidate strains belonging to the B. subtilis afford a safe, eco-friendly route to high-value POS with potent antioxidant and anticancer activities, opening avenues for functional foods, nutraceuticals, and sustainable pectin valorization.
Ort, förlag, år, upplaga, sidor
Elsevier, 2025. Vol. 331, artikel-id 148501
Nyckelord [en]
Pectin degradation, Pectic oligosaccharides (POS), probiotic candidate, Bacillus subtilis HA1
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Identifikatorer
URN: urn:nbn:se:hb:diva-34492DOI: 10.1016/j.ijbiomac.2025.148501ISI: 001607874300020Scopus ID: 2-s2.0-105019375264OAI: oai:DiVA.org:hb-34492DiVA, id: diva2:2010025
Forskningsfinansiär
Forskningsrådet Formas, 2023-020182025-10-292025-10-292026-01-30Bibliografiskt granskad