TY - JOUR
T1 - Broad-spectrum bioactivities of a sulfated heteropolysaccharide from Bacillus tequilensis MYG163
T2 - antioxidant, anti-Inflammatory, anticancer, antimicrobial, and antibiofilm properties
AU - Alwaili, Maha Abdullah
AU - Alshehri, Mohammed A.
AU - Abdulrahman, Thanaa R.
AU - Albaqami, Faisal Miqad K.
AU - Alghamdi, Abdullah
AU - Albureikan, Mona Othman I.
AU - Shamrani, Taghreed
AU - Albelasi, Abdullah
AU - El-Nablaway, Mohammad
AU - Selim, Samy
AU - Ghareeb, Ahmed
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2025
Y1 - 2025
N2 - A novel exopolysaccharide (EPS-R1) from the Red Sea bacterium Bacillus tequilensis MYG163 was isolated and characterized. The strain produced 6.33 g/l of EPS-R1, which was identified as a sulfated heteropolysaccharide containing uronic acid, N-acetyl glucose amine, and various monosaccharides. EPS-R1 showed strong antioxidant properties (>80% in DPPH and ABTS assays) and anti-inflammatory effects on COX-1 (IC50 = 25.74 µg/mL) and COX-2 (IC50 = 48.57 µg/mL). While safe for normal cells, it demonstrated cytotoxicity against colon (IC50 = 203.25 µg/mL) and pancreatic cancer cells (IC50 = 122.99 µg/mL). The compound effectively inhibited Candida albicans (MIC = 15.62 µg/mL) and showed superior antibacterial activity compared to gentamicin against Enterococcus faecalis (33 mm vs. 30 mm) and Klebsiella pneumoniae (42 mm vs. 17 mm). It significantly reduced bacterial biofilm formation (86-88% inhibition at 75% MBC) and Candida biofilms (60-90% reduction). These diverse bioactivities suggest EPS-R1's potential as a therapeutic agent.
AB - A novel exopolysaccharide (EPS-R1) from the Red Sea bacterium Bacillus tequilensis MYG163 was isolated and characterized. The strain produced 6.33 g/l of EPS-R1, which was identified as a sulfated heteropolysaccharide containing uronic acid, N-acetyl glucose amine, and various monosaccharides. EPS-R1 showed strong antioxidant properties (>80% in DPPH and ABTS assays) and anti-inflammatory effects on COX-1 (IC50 = 25.74 µg/mL) and COX-2 (IC50 = 48.57 µg/mL). While safe for normal cells, it demonstrated cytotoxicity against colon (IC50 = 203.25 µg/mL) and pancreatic cancer cells (IC50 = 122.99 µg/mL). The compound effectively inhibited Candida albicans (MIC = 15.62 µg/mL) and showed superior antibacterial activity compared to gentamicin against Enterococcus faecalis (33 mm vs. 30 mm) and Klebsiella pneumoniae (42 mm vs. 17 mm). It significantly reduced bacterial biofilm formation (86-88% inhibition at 75% MBC) and Candida biofilms (60-90% reduction). These diverse bioactivities suggest EPS-R1's potential as a therapeutic agent.
KW - Microbial metabolites
KW - anti-candidiasis
KW - antifungal
KW - antimicrobial resistance
KW - drug discovery
KW - natural products
UR - http://www.scopus.com/inward/record.url?scp=85213967202&partnerID=8YFLogxK
U2 - 10.1080/16583655.2024.2447151
DO - 10.1080/16583655.2024.2447151
M3 - Article
AN - SCOPUS:85213967202
SN - 1658-3655
VL - 19
JO - Journal of Taibah University for Science
JF - Journal of Taibah University for Science
IS - 1
M1 - 2447151
ER -