具有抗炎和抗菌活性的脂肽生物表面活性剂的优化生产

Q2 Pharmacology, Toxicology and Pharmaceutics
Salima Djafri-Dib, Yalaoui-Guellal Drifa, N. Amessis-Ouchemoukh, K. Madani, S. Ouchemoukh
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引用次数: 0

摘要

生物表面活性剂是一种非常重要的双亲化合物,具有低毒性、生物可降解性以及多种生物特性等令人感兴趣的优点。在本研究中,使用不同的检测方法评估了由水生藻类嗜盐菌(Alcaligenes aquatilisYGD 2906)生产的生物表面活性剂 BLA 2906 的抗菌和抗炎活性,以确定其生物特性。使用 PBD 和 SRM 对主题ium 中的组分浓度进行了筛选和优化,以提高表面活性剂的乳化活性值(E24%)。这些结果表明,BLA 2906 可用作一种新的治疗和抗炎剂。PBD 从筛选出的 14 种成分中选出了 7 种重要成分。在优化介质中,RSM 产生了 68.37% 的乳化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization of Lipopeptide Biosurfactant Production with Anti-Inflammatory and Antimicrobial Activities
Biosurfactants are very important amphiphile compounds due to their interesting advantages such as low toxicity, biodegradability and also their many biological properties. In the present study, antimicrobial and anti-imflammatory activities were evaluated to determine the biological proprieties of biosurfactant BLA 2906 produced by Alcaligenes aquatilis YGD 2906 using different assays. Screening and optimization component concentrations in the medium were investigated using PBD and SRM to increase surfactant yield in term emulsification activity value (E24%). The halos of antifungal activity presented a mean value of 12.33 mm to 17.67 mm. For antibacterial activity, the diameter varied from 10.33 to 12.67 mm with a very important antiinflammatory activity using a protein denaturation method that showed a maximum inhibition of 92.79%. These results suggest that BLA 2906 may be used as a new therapeutic and antiinflammatory agent. The PBD selected 7 significant components out of the 14 screened. The RSM resulted in the production in terms of emulsification activity of 68.37% in the optimized medium.
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来源期刊
Current Bioactive Compounds
Current Bioactive Compounds Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍: The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.
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