金菖蒲茎皮对金黄色葡萄球菌和大肠杆菌的抗菌化合物研究

Q3 Pharmacology, Toxicology and Pharmaceutics Biomedical and Pharmacology Journal Pub Date : 2023-09-30 DOI:10.13005/bpj/2743
Sri Rahayu Santi, I Made Sukadana, I Gusti Agung Gede Bawa, Novi Tamauli Herawati Simalango
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引用次数: 0

摘要

本研究旨在筛选金葡萄茎皮中金黄色葡萄球菌和大肠杆菌的抑菌化合物。浸渍分块法提取活性抗菌成分,扩散法抑菌试验,柱层析法分离活性成分,液相色谱/质谱法鉴定活性组分。结果表明,350 g银果茎皮浸出22.97 g甲醇黏稠提取物,对金黄色葡萄球菌(14.75mm)有较强的抑制作用,对大肠杆菌(8.50 mm)有中等抑制作用。甲醇浓缩提取物与正己烷、氯仿、正丁醇、水的分馏结果分别为0.01;0.01;2.75 g和0.07 g提取物。根据萃取物的重量,只有正丁醇萃取物可以进一步分离。对金黄色葡萄球菌和大肠杆菌有较强的抑制带(16.50 mm),最小抑制浓度(MIC)为5%。梯度柱层析法分离正丁醇提取物(硅胶60;甲醇:氯仿(5:5;4;7:3;八4;9:1;和10:0))得到4个组分(FA、FB、FC和FD),其中FC对金黄色葡萄球菌和大肠杆菌的抑菌活性最强,在5%的浓度下抑菌带分别为7.25 mm和6.25 mm。LCMS/MS结果显示,鉴定出的5个化合物分别为麦芽醇、烟酰胺、生物芸香蛋白A、l -脯氨酸和2,3-二氨基丙酸,以及1个分子量为95.8066 g/mol的未鉴定化合物。麦芽糖醇、烟酰胺、生物链蛋白A和l -脯氨酸是抑制金黄色葡萄球菌和大肠杆菌生长的化合物。
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Antibacterial Compounds Towards Staphylococcus aureus and Escherichia coli of the Stem Bark of Inocarpus Fagigerus FoSB
This study aimed to screen the antibacterial compounds of S. aureus and E. coli on the stem bark of Inocarpus fagiferus Fosb. Extraction of active antibacterial compounds by maceration and partitioning, antibacterial tests were carried out by diffusion method, separation of compounds by column chromatography method, and identification of active fractions using LSMS/MS. The results of maceration of 350 g of Inocarpus fagiferus Fosb stem bark produced 22.97 g of methanol viscous extract which was able to strongly inhibit the growth of S. aureus bacteria (14.75mm) and medium inhibit (8.50 mm) towards E. coli. The partition results of the methanol concentrated extract respectively with n-hexane, chloroform, n-butanol, and water yielded 0.01; 0.01; 2.75, and 0.07 g extracts. Based on extract weight only n-butanol extract allows further separation. The result of antibacterial activity has shown a strong inhibition zone toward S. aureus and E. coli (16.50 mm) and with a minimum inhibitory concentration (MIC) of 5%. The result of separation n-butanol extract by gradient column chromatography (silica gel 60; methanol: chloroform (5:5; 6:4; 7:3; 8:4; 9:1; and 10:0)) yielded 4 fractions (FA, FB, FC, and FD) with FC the most active antibacterial toward S. aureus and E. coli with an inhibition zone 7.25 mm and 6.25 mm respectively at 5%. The results of LCMS/MS show 5 identified compounds known are maltol, nicotinamide, bioachanin A, L-proline, and 2,3-diamino propionic acid, as well as one unidentified compound with a molecular weight of 95.8066 g/mol. Maltol, nicotinamide, bioachanin A, and L-proline are compounds potents to inhibit the growth of S. aureus and E. coli bacteria.
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来源期刊
Biomedical and Pharmacology Journal
Biomedical and Pharmacology Journal Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
1.20
自引率
0.00%
发文量
189
期刊介绍: Biomedical and Pharmacology Journal (BPJ) is an International Peer Reviewed Research Journal in English language whose frequency is quarterly. The journal seeks to promote research, exchange of scientific information, consideration of regulatory mechanisms that affect drug development and utilization, and medical education. BPJ take much care in making your article published without much delay with your kind cooperation and support. Research papers, review articles, short communications, news are welcomed provided they demonstrate new findings of relevance to the field as a whole. All articles will be peer-reviewed and will find a place in Biomedical and Pharmacology Journal based on the merit and innovativeness of the research work. BPJ hopes that Researchers, Research scholars, Academician, Industrialists etc. would make use of this journal for the development of science and technology. Topics of interest include, but are not limited to: Biochemistry Genetics Microbiology and virology Molecular, cellular and cancer biology Neurosciences Pharmacology Drug Discovery Cardiovascular Pharmacology Neuropharmacology Molecular & Cellular Mechanisms Immunology & Inflammation Pharmacy.
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