Tapping the biosynthetic potential of marine Bacillus licheniformis LHG166, a prolific sulphated exopolysaccharide producer: structural insights, bio-prospecting its antioxidant, antifungal, antibacterial and anti-biofilm potency as a novel anti-infective lead
The escalating global threat of antimicrobial resistance necessitates prospecting uncharted microbial biodiversity for novel therapeutic leads. This study mines the promising chemical richness of LHG166, a prolific exopolysaccharide (EPSR2-7.22 g/L). It comprised 5 different monosaccharides with 48....
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Veröffentlicht in: | Frontiers in microbiology 2024-04, Vol.15, p.1385493-1385493 |
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Sprache: | eng |
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Zusammenfassung: | The escalating global threat of antimicrobial resistance necessitates prospecting uncharted microbial biodiversity for novel therapeutic leads. This study mines the promising chemical richness of
LHG166, a prolific exopolysaccharide (EPSR2-7.22 g/L). It comprised 5 different monosaccharides with 48.11% uronic acid, 17.40% sulfate groups, and 6.09% N-acetyl glucosamine residues. EPSR2 displayed potent antioxidant activity in DPPH and ABTS
, TAC and FRAP assays. Of all the fungi tested, the yeast
displayed the highest susceptibility and antibiofilm inhibition. The fungi
and
showed moderate EPSR2 susceptibility. In contrast, the fungi
and
were resistant. Among G+ve tested bacteria,
was the most susceptible, while
was the most sensitive to G-ve pathogens. Encouragingly, EPSR2 predominantly demonstrated bactericidal effects against both bacterial classes based on MBC/MIC of either 1 or 2 superior Gentamicin. At 75% of MBC, EPSR2 displayed the highest anti-biofilm activity of 88.30% against
, while for G-ve antibiofilm inhibition, At 75% of MBC, EPSR2 displayed the highest anti-biofilm activity of 96.63% against
, Even at the lowest dose of 25% MBC, EPSR2 reduced biofilm formation by 84.13% in
, 61.46% in
. The microbial metabolite EPSR2 from
LHG166 shows promise as an eco-friendly natural antibiotic alternative for treating infections and oxidative stress. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2024.1385493 |