海参分离菌培养基中抗菌原理的提取与纯化

S. Sudhan
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摘要

前言:从泰米尔纳德邦Kanyakumari地区采集的海参肠道和体腔液中分离鉴定出3种广谱产抗生素微生物,分别命名为IF32、IF52和CF42。对分离的微生物进行了生化表征,并对培养特性进行了优化(以获得最大的抗生素产量)。本研究的重点是从所选菌株的培养基中提取和纯化抗生素原理。方法:对分离菌种分别在优化的发酵培养基和最佳条件下进行抗生素发酵。过滤分离细胞后,用1-丁醇、氯仿、乙酸乙酯和己烷萃取发酵培养基。所得残留物采用圆盘平板法对金黄色葡萄球菌(MTCC 1430)进行抗生素筛选。筛选出具有抗菌活性的菌渣,以硅胶为填料,采用柱层析法对其进行纯化。收集的三种抗生素残留物的组分进行生物自写,以确保抗生素的纯化。结果:氯仿、1-丁醇和乙酸乙酯分别是IF32、IF52和CF42发酵培养物中适宜提取抗生素的溶剂。利用柱层析分离得到的馏分进行生物自拍照,确保了抗生素原理的纯化。
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Extraction and purification of antibiotic principles from the culture medium of selected microbial isolates from sea cucumber
Introduction: Three broad-spectrum antibiotic-producing microbes (named IF32, IF52, and CF42) were identified and isolated from intestinal region and coelomic fluids of sea cucumber species collected from Kanyakumari district, Tamil Nadu. Biochemical characterization of the isolated microbes and optimization of culture characteristic (for maximum antibiotic productivity) were performed. The present study focuses on extraction and purification of antibiotic principles from the culture medium of the selected isolates. Methodology: The antibiotic fermentation was carried out in the optimized fermentation medium under optimum conditions separately for the isolated species. After separation of the cells by filtration, the fermented culture media were subjected to solvent extraction using 1-butanol, chloroform, ethyl acetate, and hexane. Obtained residues were subjected to antibiotic screening against Staphylococcus aureus (MTCC 1430) by disc plate method. Purification of the selected residues which showed antibiotic activity was done by column chromatography using silica gel as packing material. Collected fractions of the three antibiotic residues were subjected to bioautography to ensure the purification of the antibiotics. Results: The results show that chloroform, 1-butanol, and ethyl acetate are found to be suitable solvents for the extraction of antibiotics from the fermented cultures of IF32, IF52, and CF42, respectively. Bioautography performed using fractions obtained from column chromatographic separation ensured the purification of the antibiotic principles.
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