Mangamuri Ushakiranmayi, Muvva Vijayalakshmi, Poda Sudhakar, Naragani Krishna, Munaganti Rajesh Kumar, Chitturi Bhujangarao, Yenamandra Venkateswarlu
Department of Botany and Microbiology, Acharya Nagarjuna University, Nagarjunanagar, Guntur, 522510, Andhra Pradesh, India.
Department of Biotechnology, Acharya Nagarjuna University, Guntur, 522510, Andhra Pradesh, India.
3 Biotech. 2016 Jun;6(1):63. doi: 10.1007/s13205-016-0398-6. Epub 2016 Feb 13.
The strain VUK-A was isolated from a sediment sample of the Coringa mangrove ecosystem was identified as Streptomyces cheonanensis based on morphological, physiological, biochemical and molecular properties. Chemical investigation of the secondary metabolites of the strain Streptomyces cheonanensis VUK-A has led to the segregation of two bioactive compounds, namely 2-Methyl butyl propyl phthalate (1) and Diethyl phthalate (2) using column chromatography. The chemical structure of the active compounds was established on the basis of spectroscopic analysis, including H NMR and C NMR spectroscopies, FTIR and EIMS. The antimicrobial activity of the bioactive compounds produced by the strain was tested against a wide variety of bacteria and fungi and expressed in terms of minimum inhibitory concentration. The compounds (1&2) were active against all the bacteria tested, and the best activity of compound 1 was recorded against Proteus vulgaris (4 µg/ml). Compounds (1&2) were active against dermatophytes and fungi but compound 1 displayed high antifungal activity against Candida albicans (8 µg/ml) and Fusarium solani (16 µg/ml) compared to standard antifungal agents. The cytotoxicity of the bioactive compound 1 was tested against MDA-MB-231, OAW-42, HeLa, and MCF-7 cell lines. The highest activity of 100 µM by compound 1 was recorded against HeLa cancer cell lines. In fact, this is the first report of 2-Methyl butyl propyl phthalate from the genus Streptomyces.
菌株VUK-A是从科林加红树林生态系统的沉积物样本中分离出来的,根据形态学、生理学、生物化学和分子特性被鉴定为忠南链霉菌。对忠南链霉菌VUK-A菌株的次生代谢产物进行化学研究,通过柱色谱法分离出两种生物活性化合物,即2-甲基丁基丙基邻苯二甲酸酯(1)和邻苯二甲酸二乙酯(2)。活性化合物的化学结构是基于光谱分析确定的,包括氢核磁共振(H NMR)和碳核磁共振(C NMR)光谱、傅里叶变换红外光谱(FTIR)和电子轰击质谱(EIMS)。测试了该菌株产生的生物活性化合物对多种细菌和真菌的抗菌活性,并以最低抑菌浓度表示。化合物(1和2)对所有测试细菌均有活性,化合物1对普通变形杆菌的活性最佳(4微克/毫升)。化合物(1和2)对皮肤癣菌和真菌有活性,但与标准抗真菌剂相比,化合物1对白色念珠菌(8微克/毫升)和茄病镰刀菌(16微克/毫升)显示出高抗真菌活性。测试了生物活性化合物1对MDA-MB-231、OAW-42、HeLa和MCF-7细胞系的细胞毒性。化合物1对HeLa癌细胞系的活性最高,为100微摩尔。事实上,这是首次从链霉菌属中报道2-甲基丁基丙基邻苯二甲酸酯。