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Novel amylomacins from seaweed-associated Bacillus amyloliquefaciens as prospective antimicrobial leads attenuating resistant bacteria
The rise in antibiotic-resistant bacterial strains prompting nosocomial infections drives the search for new bioactive substances of promising antibacterial properties. The surfaces of seaweeds are rich in heterotrophic bacteria with prospective antimicrobial substances. This study aimed to isolate...
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Published in: | World journal of microbiology & biotechnology 2021-12, Vol.37 (12), p.200-200, Article 200 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The rise in antibiotic-resistant bacterial strains prompting nosocomial infections drives the search for new bioactive substances of promising antibacterial properties. The surfaces of seaweeds are rich in heterotrophic bacteria with prospective antimicrobial substances. This study aimed to isolate antibacterial leads from a seaweed-associated bacterium. Heterotrophic
Bacillus amyloliquefaciens
MTCC 12716 associated with the seaweed
Hypnea valentiae
, was isolated and screened for antimicrobial properties against drug-resistant pathogens. The bacterial crude extract was purified and three novel amicoumacin-class of isocoumarin analogues, 11′-butyl acetate amicoumacin C (amylomacin A), 4′-hydroxy-11′-methoxyethyl carboxylate amicoumacin C (amylomacin B) and 11′-butyl amicoumacin C (amylomacin C) were isolated to homogeneity. The studied amylomacins possessed potential activities against
Pseudomonas aeruginosa
, vancomycin-resistant
Enterococcus faecalis
,
Klebsiella pneumoniae
, methicillin-resistant
Staphylococcus aureus
, and
Shigella flexneri
with a range of minimum inhibitory concentration values from 0.78 to 3.12 µg/mL, although standard antibiotics ampicillin and chloramphenicol were active at 6.25–25 µg/mL. Noticeably, the amylomacin compound encompassing 4′-hydroxy-11′-methoxyethyl carboxylate amicoumacin C functionality (amylomacin B), displayed considerably greater antagonistic activities against methicillin-resistant
S. aureus
, vancomycin-resistant
E. faecalis
,
Vibrio parahaemolyticus
,
Escherichia coli
, and
K. pneumoniae
(minimum inhibitory concentration 0.78 μg/mL) compared to the positive controls and other amylomacin analogues. Antimicrobial properties of the amylomacins, coupled with the presence of polyketide synthase-I/non-ribosomal peptide synthetase hybrid gene attributed the bacterium as a promising source of antimicrobial compounds with pharmaceutical and biotechnological applications.
Graphic abstract |
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ISSN: | 0959-3993 1573-0972 |
DOI: | 10.1007/s11274-021-03161-9 |