从卡罗托双procera球茎中提取的一些生物活性化合物的分离、鉴定、抗菌及理论研究

M. Khan, Chijioke Ezekiel Elum, A. O. Ijeomah, Hilip John Ameji, I. G. Osigbemhe, Emmanuel Etim (PhD), John Veshima Anyam, Alexander S. P. Abel, CyprianTernenge Agber
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引用次数: 0

摘要

本研究对卡罗贝球茎的生物活性分子进行了表征,并对其粗提物的抑菌活性进行了研究。对粗提物中分离的两种化合物进行了理论研究。球茎被风干、粉碎,然后分别用500毫升正己烷、乙酸乙酯和甲醇浸泡提取。采用标准程序对粗提物进行微生物和植物化学筛选测试。此外,对提取液中含有的抗两种革兰氏阴性菌DNA旋切酶活性化合物进行了筛选;利用瑞士ADME在线服务器,对大肠杆菌和伤寒沙门氏菌进行分子对接模拟技术,并进一步进行ADMET分析。乙酸乙酯粗提物对大肠杆菌(MIC为2.5mg/mL, MBC/MFC为5mg/mL)、金黄色葡萄球菌(MIC为2.5mg/mL)、白色念珠菌、伤寒沙门氏菌和星状念珠菌(MIC为5mg/mL)的抑菌活性最高。纯化后的白色结晶部分中含有β -醋酸amyrin和Taraxasterol两种植物化学物质,它们通过疏水和氢键相互作用与格兰氏阴性细菌的DNA旋合酶活性位点相连,结合活性值分别为-9.6 kcal/mol和-9.5 kcal/mol。此外,ADMET研究表明,这些化合物具有良好的口服生物利用度和良好的药代动力学和毒性谱。这项研究的发现可以为发现安全有效的抗生素来对抗危害我们社会的病原微生物提供一个平台。
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Isolation, Characterization, Antimicrobial and Theoretical Investigation of Some Bioactive Compounds Obtained from the Bulbs of Calotropisprocera
This study characterizes the bioactive molecules from the bulb of Calotropisprocera and investigates the antimicrobial activities of the crude extracts. Theoretical studies on the two isolated compounds in the crude extract were also accomplished.The bulbs were air dried, pulverized, and subjected to extraction procedures by maceration using 500 mL each of normal-hexane, ethyl acetate and methanol. The crude extracts were further tested onmicroorganisms and phytochemical screening using standard procedures. In addition, the bioactive compounds in the extract were screened against DNA gyrase of two Gram negative bacterial species; Escherichia coli and Salmonella typhiusing Molecular Docking simulation techniques and further subjected to ADMET profiling,using the Swiss ADME online server. The Crude ethyl acetate extract has the highest effective activity against Escherichia coli (MIC 2.5mg / mL and MBC/MFC 5mg / mL), Staphylococcus aureus (MIC 2.5mg/mL), Candida albicans, Salmonella typhiand Candida stellafoidea (MIC 5mg/mL). beta-Amyrin acetate and Taraxasterol are the two phytochemicals in the purified white crystalline fractions and were found to fasten to the active sites of DNA gyrase of the Gram negative bacterial species via hydrophobic and hydrogen bond interactions, with binding activity value of -9.6 kcal/mol and -9.5 kcal/mol, respectively. Also, ADMET investigations of the compounds revealed their sound oral bioavailability and excellent pharmacokinetic and toxicity profiles. The findings of this study could provide a platform for discovering safe and potent antibiotics against pathogenic microbes ravaging our society.
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