Isolation and identification of Garciyunnanensisin A-O from Garcinia yunnanensis: a study on its antibacterial activity and mechanism against Staphylococcus aureus.
Peng-Xue Ji, Zhi-Yuan Li, Sheng-Nan Yang, Si-Han Wang, Yun Gao, Zi-Feng Guo, Jing-Ming Jia, Shao-Hui Huang, Zhen-Zhong Wang, An-Hua Wang
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引用次数: 0
Abstract
Staphylococcus aureus has a strong biofilm-forming ability that protects it from the external environment, making it difficult to remove during food processing and storage, thereby increasing the incidence of foodborne illness. In order to improve food safety and protect human health, it is important to find safe and effective antimicrobial agents. In this study, a total of 20 compounds (1-20), including 15 new compounds (1-15), were isolated from Garcinia yunnanensis and elucidated by Nuclear Magnetic Resonance (NMR) data analysis, calculation of optical rotation values, and Electronic Circular Dichroism (ECD) spectra. Compound 1, a rare caged polycyclic polyprenylated acylphloroglucinol, demonstrated significant antibacterial activity against S. aureus with a minimum inhibitory concentration (MIC) of 6.25 μg/mL and showed rapid bactericidal effects at high concentrations. In addition, 1 inhibited S. aureus biofilm formation by reducing bacterial metabolism, decreasing bacterial viability, inhibiting bacterial surface hydrophobicity and adhesion, and modulating the synthesis and secretion of extracellular polysaccharides, DNA, and proteins. Scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) also further confirmed that 1 significantly inhibited biofilm formation. In conclusion, 1 not only has excellent antibacterial and biofilm inhibitory properties, but also exhibits low toxicity, making it a promising candidate for development as a food-grade bacterial biofilm inhibitor.
期刊介绍:
Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry.
For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature.
The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.