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首页> 外文期刊>Universitas Gadjah Mada >Antibacterial Compound Identification of Cayenne Pepper Leaf Extract (Capsicum frutescens L.) against Klebsiella pneumoniae and Cell Leakage Mechanism
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Antibacterial Compound Identification of Cayenne Pepper Leaf Extract (Capsicum frutescens L.) against Klebsiella pneumoniae and Cell Leakage Mechanism

机译:辣椒叶片提取物(辣椒)对肺炎克雷伯菌的抗菌化合物鉴定及细胞泄漏机制

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Pneumonia is an acute inflammation of the pulmonary parenchyma that can be caused by Klebsiella pneumoniae. This study aims to determine the active fraction of cayenne pepper leaves on the growth of K. pneumoniae . Cayenne pepper leaf which previously defatted using n-hexane was macerated with 95% ethanol, then fractionated successively with dichloromethane, ethyl acetate and methanol. Ethanol extract and each fraction with concentration of 40% were tested for their antibacterial activity against K. pneumoniae using disc diffusion method (Kirby-Bauer). 1% amoxicillin was used as positive control and Dimethyl sulfoxide (DMSO) as negative control. The Minimum Inhibitory Concentration (MIC) of the most active fraction was then determined. Determination of antibacterial compound in the most active fraction was carried out by TLC-bioautography and followed by Gass Chromatography Mass Spectrophotometry. Cell leakage analysis was performed using UV spectrophotometry to detect the release of protein and nucleic acid, as well as Atomic Absorption Spectrophotometry was used to detect ion release of K+ and Ca2+. The results showed that the most active fraction against K. pneumoniae was the ethyl acetate fraction with MIC value of 10% and inhibition zone of 7.25±0.25 mm. TLC-Bioautography of ethyl acetate fraction with eluen n-hexane: ethyl acetate (6:4) obtained an active stain at Rf 0.12. Compounds having 94% similarity with 1-propanol, 2-amino was predicted as the active compound.
机译:肺炎是由肺炎克雷伯菌引起的肺实质的急性炎症。这项研究旨在确定辣椒叶片对肺炎克雷伯菌生长的活性成分。将预先用正己烷脱脂的辣椒叶片浸入95%的乙醇中,然后依次用二氯甲烷,乙酸乙酯和甲醇分馏。使用圆盘扩散法(Kirby-Bauer),测试乙醇提取物和浓度为40%的各个级分对肺炎克雷伯菌的抗菌活性。 1%阿莫西林用作阳性对照,二甲基亚砜(DMSO)作为阴性对照。然后确定活性最高的组分的最小抑制浓度(MIC)。活性最高的部分中的抗菌化合物的测定通过TLC-生物自显影技术进行,然后通过气相色谱质谱法进行。使用紫外分光光度法进行细胞泄漏分析,以检测蛋白质和核酸的释放,并使用原子吸收分光光度法检测K +和Ca2 +的离子释放。结果表明,对肺炎克雷伯菌最具活性的组分是乙酸乙酯,其MIC值为10%,抑制区为7.25±0.25 mm。用洗脱液正己烷:乙酸乙酯(6∶4)对乙酸乙酯部分进行TLC-生物自显影,在Rf 0.12下获得活性染料。预测与1-丙醇,2-氨基具有94%相似性的化合物为活性化合物。

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