Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/112899
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorZhi, Zen_US
dc.creatorZhou, Pen_US
dc.creatorHe, Ten_US
dc.creatorChen, Sen_US
dc.creatorQian, Xen_US
dc.creatorYe, Yen_US
dc.creatorWong, WLen_US
dc.creatorLi, Sen_US
dc.creatorSun, Nen_US
dc.creatorYuan, Wen_US
dc.date.accessioned2025-05-12T08:48:02Z-
dc.date.available2025-05-12T08:48:02Z-
dc.identifier.issn0006-291Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/112899-
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.subjectAntibacterial activityen_US
dc.subjectCarvacrolen_US
dc.subjectDrug-resistant bacteriaen_US
dc.subjectFtsZ inhibitoren_US
dc.titleStudy of the antimicrobial activity of carvacrol and its mechanism of action against drug-resistant bacteriaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume757en_US
dc.identifier.doi10.1016/j.bbrc.2025.151643en_US
dcterms.abstractDrug-resistant bacterial infections have been one of the critical health issues encountered worldwide currently because most conventional antibiotics are losing their effectiveness in clinical treatments. It is thus urgently to identify new antibiotics or alternatives against drug-resistant bacteria. For this purpose, we attempted to seek active compounds from commercially available natural products, which may be one of the fast-tracks to address the drug-resistant bacterial infections. In the present study, we investigated the antibacterial activity, antibacterial mechanism and synergistic effects of carvacrol against a panel of drug-resistant bacteria, including some clinical isolates. The results show that carvacrol (cymophenol), a monoterpenoid phenol, has excellent antibacterial activity. The MIC values against the bacteria examined are found to be 4–16 μg/mL. Our results also suggested that carvacrol might not likely to induce drug-resistance. More importantly, when carvacrol combined with first-line antibiotics, it exhibited good synergistic effects against drug-resistant bacteria. Moreover, in morphological studies, carvacrol could cause B. subtilis 168 elongation and S. aureus BAA-41 enlargement, which may suggest an antibacterial mechanism possibly correlated with the inhibition of bacterial cell division. We further demonstrated that carvacrol facilitated the polymerization of FtsZ that is a critically important protein for regulating bacterial cell division. Furthermore, molecular modeling predicted that carvacrol could interact with T7-loop of FtsZ. The findings of this study suggest that carvacrol may be a potential inhibitor of FtsZ and it could be utilized to combat drug-resistant bacteria in combination with existing antibiotics.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationBiochemical and biophysical research communications, 9 Apr. 2025, v. 757, 151643en_US
dcterms.isPartOfBiochemical and biophysical research communicationsen_US
dcterms.issued2025-04-09-
dc.identifier.eissn1090-2104en_US
dc.identifier.artn151643en_US
dc.description.validate202505 bcchen_US
dc.description.oaNot applicableen_US
dc.identifier.FolderNumbera3588-
dc.identifier.SubFormID50411-
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-04-09en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2026-04-09
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