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Separation of cordycepin from Cordyceps militaris fermentation supernatant using preparative HPLC and evaluation of its antibacterial activity as an NAD(+)-dependent DNA ligase inhibitor

机译:使用制备型HPLC从y虫草发酵上清液中分离虫草素并评估其作为NAD(+)依赖性DNA连接酶抑制剂的抗菌活性

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摘要

Cordycepin exhibits various bio-activities, including anticancer, antibacterial, antiviral and immune regulation activities, and is a significant focus of research. However, the preparation of high-purity cordycepin remains challenging. Also, the molecular target with which cordycepin interacts to cause an antibacterial effect remains unknown. In the present study, cordycepin was prepared by preparative high-performance liquid chromatography (prep-HPLC) and the purity obtained was 99.6%, indicating that this technique may be useful for the large-scale isolation of cordycepin in the future. The results of computational molecular docking analysis indicated that the interaction energy between cordycepin and NAD+-dependent DNA ligase (LigA) was lower than that between cordycepin and other common antibacterial targets. The highly pure cordycepin obtained by prep-HPLC demonstrated inhibitory activity against LigA from various bacteria in vitro. In conclusion, cordycepin may be useful as a broad-spectrum antibiotic targeting LigA in various bacteria.
机译:虫草素具有多种生物活性,包括抗癌,抗菌,抗病毒和免疫调节活性,是研究的重点。然而,高纯度虫草素的制备仍然具有挑战性。而且,与虫草素相互作用以引起抗菌作用的分子靶仍然是未知的。在本研究中,虫草素是通过制备型高效液相色谱法制备的,所获得的纯度为99.6%,表明该技术可能在将来大规模分离虫草素中有用。计算分子对接分析的结果表明,虫草素和NAD +依赖性DNA连接酶(LigA)之间的相互作用能比虫草素和其他常见抗菌靶标之间的相互作用能低。通过制备型HPLC获得的高纯度虫草素在体外显示出对各种细菌对LigA的抑制活性。总之,虫草素可能作为靶向多种细菌中LigA的广谱抗生素。

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