孢子链霉菌生物活性物质的结构鉴定及其生物活性(病原微生物和细胞毒性)

Dina Elghwas, Hind Elghwas, Fatimah Alshehrei, Amr El-Waseif
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摘要

属于链霉菌属的丝状细菌因其生成多种生物可用的次级代谢产物的卓越能力而闻名。在这项工作中,使用从沙特阿拉伯延布市分离的 Streptomyces sp.根据 16S 核糖体 RNA 序列同源性研究,它与 sporaveus 链霉菌 AD 4 有 99% 的相同之处。使用乙酸乙酯提取发酵液后,使用高效液相色谱法(HPLC)检测粗提取物的纯度。经过纯化阶段,分离出三种纯生物活性馏分,分别命名为 A、B 和 C,保留时间分别为 2.251 ± 0.3 分钟、4.342 ± 0.3 分钟和 5.988 ± 0.3 分钟。此外,还对这三种化合物进行了光谱检测,包括其 GC-MS 数据,通过与已发表的参考数据进行比较,确定了它们的化学结构。此外,这三种馏分对伤寒沙门氏菌(ATCC 14028)、白色念珠菌、黑曲霉、肺炎克雷伯氏菌、铜绿假单胞菌(ATCC 9027)、表皮葡萄球菌、黄体小球菌、大肠杆菌(ATCC 8739)和枯草杆菌(ATCC 6633)具有很强的抗菌活性。此外,还使用 Hct-116 株系评估了生物活性馏分的细胞毒性。在三种馏分中,馏分 C 的细胞毒性最低,IC50 值为 224.57 ± 5.82,其次是馏分 B(238.82 ± 2.57)和馏分 A(341.28 ± 1.69)。
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STRUCTURE ELUCIDATION OF BIOACTIVE MATERIAL FROM STREPTOMYCES SPORORAVEUS AND ITS BIOLOGICAL ACTIVITY (PATHOGENIC MICROORGANISMS AND CYTOTOXICITY)
Filamentous bacteria belonging to the Streptomyces genus are well known for their exceptional capacity to generate a diverse range of bioavailable secondary metabolites. In this work, an inoculum for fermentation was created using Streptomyces sp., which was isolated from Yanbu City, Saudi Arabia. It was 99% identical to Streptomyces spororaveus AD 4, according to 16S ribosomal RNA sequence homology studies. After using ethyl acetate to extract the fermented broth, the crude extract's purity was checked using high-performance liquid chromatography (HPLC). Following the purification stages, three pure bioactive fractions were isolated and given the names A, B, and C, with retention times of 2.251 ± 0.3 min, 4.342 ± 0.3 min, and 5.988 ± 0.3 min, respectively. Additionally, the spectroscopic examinations of these three compounds, including their GC-MS data, were used to determine their chemical structures by comparing them to published reference data. Additionally, the three fractions exhibit potent antimicrobial activity against Salmonella typhi ATCC 14028, Candida albicanc, Aspergillus niger, Klebsiella pneumoniae, Pseudomonas aeruginosa ATCC 9027, Staphylococcus epidermidis, Micrococcus luteus, E. coli ATCC 8739, and B. subtilis ATCC 6633. Also, the cytotoxicity of the bioactive fractions was assessed using the Hct-116 line. Of the three fractions, fraction C had the lowest cytotoxicity, with an IC50 value of 224.57 ± 5.82, followed by fraction B at 238.82 ± 2.57 and fraction A at 341.28 ± 1.69.
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