海洋沉积物新放线菌色链霉菌SU5细胞毒性化合物的研究

S. Sudha, M. Masilamani Selvam
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摘要

在寻找新的抗癌化合物的过程中,我们主动从泰米尔纳德邦海岸分离出嗜盐放线菌。从Pulicat、enore、Muttukadu和Veerampattinam沿海土壤样品中分离出52种放线菌。对52株分离株中仅有10株进行了盐水对虾致死试验,并对其中一株最具细胞毒性的维仑帕丁菌进行了进一步研究。活性分离物粗提物对Hep-2细胞株的LC50值为62.5µg,为60;VERO细胞系中250µg。粗提物经薄层色谱纯化,GC-MS表征。化合物邻苯二甲酸二异丁酯(16.82%)和1,2-苯二甲酸,双(2-乙基己基)酯(65.26%)富集,保留时间分别为15.645和21.620。形态学、培养、生理生化及16s rRNA测序结果鉴定该活性菌株为链霉菌(Streptomyces colelicolor),并已提交GENBANK。由此推测,深蓝链霉菌SU5菌株可产生抗癌化合物,这些化合物可进一步加工用于商业应用。该研究清楚地证明了具有生物活性代谢物的海洋沉积物衍生放线菌有望为高通量生化和抗癌筛选项目提供高质量的生物材料。
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Characterization of cytotoxic compound from marine sediment derived new actinomycete Streptomyces coelicolor strain SU5
In the search of novel anticancer compounds we have taken an initiative to isolate halophilic actinomycetes from Tamilnadu coast. Fifty-two actinomycetes were isolated from the coastal soil samples of Pulicat, Ennore, Muttukadu, and Veerampattinam. Out of 52 isolates only 10 were subjected to brine shrimp lethality assay and one of the most potent cytotoxic isolate, which is the inhabitant of Veerampattinam was studied further. Crude extract of the active isolate exhibited LC50 in 62.5 µg against Hep-2 cell line, < 250µg in VERO cell line. The crude extract was purified by TLC and then characterized by using GC-MS. The following compounds diisobutyl phthalate (16.82%) and 1,2-Benzenedicaarboxylic acid, Bis(2-ehtylehexyl) ester (65.26%) were found abundantly with retention time 15.645, 21.620 respectively. Morphological, cultural, physiological, biochemical assay and 16s rRNA sequencing results the active strain was identified as Streptomyces and closely related to the species Streptomyces coelicolor also submitted to GENBANK. It is inferred that Streptomyces coelicolor strain SU5 producing anticancer compounds and these may be processed further for its commercial application. This study clearly proves that the marine sediment derived actinomycetes with bioactive metabolites can be expected to provide high quality biological material for high throughout biochemical and anticancer screening programs.
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