Ozoroa insignis reticulata (Baker f.) R. Fern. & A.Fern.根提取物可抑制金黄色葡萄球菌产生胞外蛋白酶。

IF 3.4 Q2 BIOCHEMICAL RESEARCH METHODS
Biochemistry Research International Pub Date : 2021-10-29 eCollection Date: 2021-01-01 DOI:10.1155/2021/5599129
Jonathan Katsukunya, Rumbidzai Makurira, Stanley Mukanganyama
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引用次数: 0

摘要

由于耐药菌株的紧急出现,治疗由金黄色葡萄球菌引起的感染已成为一项挑战。在津巴布韦,Ozoroa reticulata 根提取物一直被用于治疗喉咙和胸痛的传统医学中。本研究的目的是确定 O. reticulata 根皮提取物对金黄色葡萄球菌产生胞外蛋白酶的影响。采集根皮,将其干燥并碾成粉末。为了获得不同的植物成分,进行了植物萃取。萃取使用两种混合溶剂:乙醇:水(50:50 v/v)和二氯甲烷:甲醇(50:50 v/v)。此外,还使用甲醇、乙醇、二氯甲烷、丙酮、乙酸乙酯、正己烷和水进行了连续穷举提取。肉汤微量稀释法用于评估 Ozoroa 网纹根树皮提取物对金黄色葡萄球菌的抗菌效果。环丙沙星用作阳性对照。在卡介苗-金黄色葡萄球菌琼脂平板上,使用最有效的提取物对金黄色葡萄球菌产生的胞外蛋白酶进行定性筛选。对蛋白水解区进行了测量,并以菌落直径与菌落直径加水解区总直径之比(P z 值)表示。研究发现,乙酸乙酯提取物是金黄色葡萄球菌生长的最有效抑制剂,抑制率达 99%,最低抑制浓度 (MIC) 为 100 µg/mL。对细胞外蛋白酶生成的抑制作用与提取物的浓度成正比。当浓度为 100 µg/mL 时,乙酸乙酯提取物的 P z 值为 0.84,表明其具有轻微的蛋白水解活性。浓度为 200 µg/mL 时,P z 值为 0.94,表明蛋白水解活性较弱。总之,该提取物抑制了金黄色葡萄球菌胞外蛋白酶的产生。进一步分离和纯化能抑制细胞外蛋白酶产生的生物活性化合物,对于发现对金黄色葡萄球菌具有抗病毒作用的制剂具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>Ozoroa insignis reticulata</i> (Baker f.) R. Fern. & A. Fern. Root Extract Inhibits the Production of Extracellular Proteases by <i>Staphylococcus aureus</i>.

<i>Ozoroa insignis reticulata</i> (Baker f.) R. Fern. & A. Fern. Root Extract Inhibits the Production of Extracellular Proteases by <i>Staphylococcus aureus</i>.

<i>Ozoroa insignis reticulata</i> (Baker f.) R. Fern. & A. Fern. Root Extract Inhibits the Production of Extracellular Proteases by <i>Staphylococcus aureus</i>.

Ozoroa insignis reticulata (Baker f.) R. Fern. & A. Fern. Root Extract Inhibits the Production of Extracellular Proteases by Staphylococcus aureus.

Treatment of infections caused by S. aureus has become a challenge due to the emergency of resistant strains. Ozoroa reticulata root extracts have been used in traditional medicine to treat throat and chest pains in Zimbabwe. The objective of the study was to determine the effects of O. reticulata root bark extracts on the production of extracellular proteases by S. aureus. The root barks were collected, dried, and crushed into powder. To obtain different phytoconstituents, plant extractions were performed. Extractions were carried out using two solvent mixtures: ethanol : water (50 : 50 v/v) and dichloromethane : methanol (50 : 50 v/v). Serial exhaustive extractions were also performed using methanol, ethanol, dichloromethane, acetone, ethyl acetate, hexane, and water. The broth microdilution assays were used to assess the antibacterial effects of the Ozoroa reticulata root bark extracts against S. aureus. Ciprofloxacin was used as a positive control. Qualitative screening for extracellular protease production by S. aureus on BCG-skim milk agar plates using the most potent extract was carried out. The proteolytic zones were measured and expressed as the ratio of the diameter of the colony to the total diameter of the colony plus the zone of hydrolysis (P z values). The ethyl acetate extract was found to be the most potent inhibitor of the growth of S. aureus with 99% inhibition and a minimum inhibitory concentration (MIC) of 100 µg/mL. Inhibition of extracellular protease production was directly proportional to the concentration of the extract. At 100 µg/mL, the ethyl acetate extract had a P z value of 0.84, indicative of mild proteolytic activity. A P z value of 0.94 was observed at a concentration of 200 µg/mL and signified weak proteolytic activity. In conclusion, the extract inhibited the production of extracellular proteases in S. aureus. Further work on the isolation and purification of bioactive compounds responsible for inhibiting the production of extracellular proteases is of importance in the discovery of agents with antivirulent effects on S. aureus.

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Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
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