Degradation of pectin with probiotic candidate Bacillus subtilis HA1 to oligosaccharides with enhanced anticancer and antioxidant properties
2025 (English)In: International Journal of Biological Macromolecules, ISSN 0141-8130, E-ISSN 1879-0003, Vol. 331, article id 148501Article in journal (Refereed) 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.
Place, publisher, year, edition, pages
Elsevier, 2025. Vol. 331, article id 148501
Keywords [en]
Pectin degradation, Pectic oligosaccharides (POS), probiotic candidate, Bacillus subtilis HA1
National Category
Food Science
Research subject
Resource Recovery
Identifiers
URN: urn:nbn:se:hb:diva-34492DOI: 10.1016/j.ijbiomac.2025.148501Scopus ID: 2-s2.0-105019375264OAI: oai:DiVA.org:hb-34492DiVA, id: diva2:2010025
Funder
Swedish Research Council Formas, 2023-020182025-10-292025-10-292025-11-03Bibliographically approved