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Biological Activity of : A Source of Potential Antimicrobial Compounds against . | LitMetric

Biological Activity of : A Source of Potential Antimicrobial Compounds against .

Int J Mol Sci

Department of Chemical Engineering, Faculty of Chemistry and Chemical Engineering, Babeş-Bolyai University, 11 Arany Janos Street, RO-400028 Cluj-Napoca, Romania.

Published: November 2022

AI Article Synopsis

  • Yersiniosis, a significant zoonotic disease in Europe, is caused by a pathogen that is notably antibiotic-resistant, prompting the exploration of herbal extracts for antimicrobial properties.
  • An ethanolic extract from a specific herb demonstrated considerable antimicrobial effectiveness, highlighted by a 29.8 mm inhibition zone and was able to reduce the pathogen's live cell count and toxin production.
  • The bioactive compound picroside-1 was identified as a strong antimicrobial agent, exhibiting higher potency than standard antibiotics, and shows promise as a potential drug candidate due to its interactions with the dihydrofolate reductase protein.

Article Abstract

Yersiniosis, caused by , is the third most rampant zoonotic disease in Europe; the pathogen shows high antibiotic resistance. Herbs have multiple anti-microbial components that reduce microorganism resistance. Therefore, an extract of () was evaluated for potential antimicrobial activity. We report that the ethanolic extract of showed effective antimicrobial activity (zone of inhibition: 29.8 mm, Minimum inhibitory concentration (MIC): 2.45 mg/mL, minimum bactericidal concentration (MBC): 2.4 mg/mL) against . Potential bioactive compounds from were identified using LC-MS, namely, cerberidol, annonidine A, benzyl formate, picroside-1, and furcatoside A. showed effective antimicrobial potential in skim milk at different pH, acidity, and water activity levels. affected the physiology of and reduced the number of live cells. , when incubated with extract, showed lower toxin production. Picroside-1 was isolated and showed higher antimicrobial potential in comparison to the standard antibiotic. Picroside-1 lysed the cells, as observed under scanning electron microscopy. Docking revealed that picroside-1 (ligand) showed both hydrophilic and hydrophobic interactions with the dihydrofolate reductase (DHFR) protein of and that DHFR is a possible drug target. The high activity and natural origin of Picroside-1 justify its potential as a possible drug candidate for .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694339PMC
http://dx.doi.org/10.3390/ijms232214090DOI Listing

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