Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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() is highly infectious and harmful, causing serious damage to human health and economic losses. Plant-derived component plumbagin (PLB) is regarded as an alternative to traditional fungicides for its natural, safe, and strong antimicrobial activity. In this study, the antibacterial activity and mechanism of PLB against were investigated by membrane damage measurement, metabolomics, and molecular docking. Results showed that PLB significantly inhibited the growth and reproduction of on NA plates and in milk with the minimum inhibitory concentration of 31.25 mg L. PLB impaired cell membrane structure and function, as indicated by disruption of bacterial morphology observed by SEM, increased red fluorescence of PI staining, and higher extracellular conductivity, k, and nucleic acid content. Moreover, PLB treatment increased ROS levels and MDA content, and decreased antioxidant enzyme activities (CAT and SOD), intracellular total lipids, total sugars and total proteins in . Metabolomics analysis indicated that PLB treatment caused 58 increased and 31 decreased metabolites in , severely affecting pathways of protein synthesis, lipid metabolism, TCA cycle, ABC transport, etc. Molecular docking showed that PLB has binding potential to key proteases involved in differential metabolite formation in the TCA cycle, glutathione metabolism, and lysine degradation, suggesting that the exertion of antibacterial activity of PLB may be associated with the disruption of these proteins. The above result indicates that PLB inhibited through membrane damage, and material and energy metabolism disruption, which provides a theoretical basis for PLB as novel preservation.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12148597 | PMC |
http://dx.doi.org/10.1016/j.crfs.2025.101083 | DOI Listing |