北苏拉威西万鸦老湾花柱海绵提取物的抑菌活性研究

Irpan Palungan, R. Bara, R. E. Mangindaan, Kurnia Kemer, S. Wullur, U. Rembet
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引用次数: 0

摘要

海绵中含有的次生代谢物具有独特的化学结构和非常有趣的药理活性,如抗菌、抗癌、抗病毒等有待开发的候选药物。生物活性代谢物在海绵等无固定物中的存在,也反映了该生物在长期进化过程中形成的生态适应性,作为该生物与环境的一种防御机制,其形式为抵抗捕食、竞争和感染因素,以对抗致病菌。因此,本研究旨在检测柱花海绵馏分提取物和馏分的抑菌活性,并测定其最低抑菌浓度(MIC)和最低杀菌浓度(MBC)值。测定抗菌活性的方法为琼脂扩散法(圆盘扩散Kirby - Bauer法)。在培养24小时后,纸圆盘周围形成一个清晰的区域,表明存在抗菌活性。结果表明:海绵提取液对巨型芽孢杆菌DSM32T的抑菌活性在21 mm处表现为最强抑制区;进一步测试表明,半极性部分对巨芽孢杆菌有较强的抑制作用,极性部分对巨芽孢杆菌有中等抑制作用,非极性部分对巨芽孢杆菌无抑制作用。分别在500ppm和1000ppm下测定了MIC和MBC值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibacterial Activity of Stylissa carteri Sponge Extract from Manado Bay, North Sulawesi
Marine sponges contain secondary metabolites with unique chemical structures and very interesting pharmacological activities, such as antibacterial, anticancer, antiviral and others to be developed as candidate drugs. The presence of bioactive metabolites in sessile nature such as sponges also reflects the ecological adaptation formed during a long evolutionary process as a defense mechanism of this organism with its environment in the form of resistance to predation, competition and infection factors against pathogenic bacteria, so this study aims to examine the antibacterial activity of extracts and fractions of Stylissa carteri sponge fractions as well as testing the Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) values. The method used in testing the antibacterial activity is the agar diffusion method (Disc Diffusion Kirby Bauer Method). The presence of antibacterial activity was indicated by the formation of a clear zone around the paper disc after incubation for 24 hours. The results showed that antibacterial activity of S. carteri sponge extract tested on Bacillus megaterium DSM32T bacteria revealed to be the strongest inhibition zone of 21 mm. Further testing on the extract fraction of S. carteri showed that the semipolar fractions showed strong activity against the B. megaterium while the polar fraction was categorized as moderate action, the non-polar fraction showed no activity against the bacteria. The determination of the MIC and MBC values was obtained at 500 ppm and 1000 ppm respectively.
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