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阿扎霉素 F 抗耐甲氧西林金黄色葡萄球菌的机制。

Mechanism of Azalomycin F against Methicillin-Resistant .

机构信息

College of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang, Jiangxi 330045, China.

Affiliated Hospital of Jiangxi Agricultural University, Nanchang, Jiangxi 330045, China.

出版信息

Biomed Res Int. 2018 Jan 21;2018:6942452. doi: 10.1155/2018/6942452. eCollection 2018.

Abstract

To investigate the mechanism of azalomycin F against methicillin-resistant (MRSA), the conductivity of MRSA suspension and the adenylate kinase activity of MRSA culture were determined with the intervention of azalomycin F, which were significantly increased compared to those of blank controls. This inferred that azalomycin F could lead to the leakage of cellular substances possibly by increasing permeability to kill MRSA. As phospholipid bilayer was mainly responsible for cell-membrane permeability, the interaction between azalomycin F and cell-membrane lipids was further researched by determining the anti-MRSA activities of azalomycin F combined with cell-membrane lipids extracted from test MRSA or with 1,2-dipalmitoyl--glycero-3-phospho-glycerol (DPPG) for possible molecular targets lying in MRSA cell-membrane. The results indicated that the anti-MRSA activity of azalomycin F remarkably decreased when it combined with membrane lipids or DPPG. This indicated that cell-membrane lipids especially DPPG might be important targets of azalomycin F against MRSA.

摘要

为了研究阿扎霉素 F 对耐甲氧西林金黄色葡萄球菌(MRSA)的作用机制,用阿扎霉素 F 干预后测定了 MRSA 悬浮液的电导率和 MRSA 培养液中的腺苷酸激酶活性,与空白对照组相比,这两项均显著升高。这推断出阿扎霉素 F 可能通过增加通透性导致细胞物质泄漏,从而杀死 MRSA。由于磷脂双层主要负责细胞膜通透性,因此通过测定阿扎霉素 F 与从试验性 MRSA 中提取的细胞膜脂质或 1,2-二棕榈酰基-sn-甘油-3-磷酸甘油(DPPG)结合后的抗 MRSA 活性,进一步研究了阿扎霉素 F 与细胞膜脂质的相互作用,以确定可能位于 MRSA 细胞膜上的分子靶标。结果表明,当阿扎霉素 F 与膜脂质或 DPPG 结合时,其抗 MRSA 活性显著降低。这表明细胞膜脂质,尤其是 DPPG,可能是阿扎霉素 F 抗 MRSA 的重要靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0ec/5828411/099f80e1e15d/BMRI2018-6942452.001.jpg

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