Shetty Prakasham Reddy, Buddana Sudheer Kumar, Tatipamula Vinay Bharadwaj, Naga Yaswanth Varanasi Venkata, Ahmad Jamal
Bioengineering and Environmental Centre Indian Institute of Chemical Technology Hyderabad India.
Braz J Microbiol. 2014 Apr 8;45(1):303-12. doi: 10.1590/S1517-83822014005000022. eCollection 2014.
A highly potent secondary metabolite producing actinomycetes strain is isolated from marine soil sediments of Visakhapatnam sea coast, Bay of Bengal. Over all ten strains are isolated from the collected soil sediments. Among the ten actinomycetes strains the broad spectrum strain RSPSN2 was selected for molecular characterization, antibiotic production and its purification. The nucleotide sequence of the 1 rRNA gene (1261 base pairs) of the most potent strain evidenced a 96% similarity with Streptomyces parvulus 1044 strain, Streptomyces parvulus NBRC 13193 and Streptomyces parvulus BY-F. From the taxonomic features, the actinomycetes isolate RSPSN2 matches with Streptomyces parvulus in the morphological, physiological and biochemical characters. Thus, it was given the suggested name Streptomyces parvulus RSPSN2. The active metabolite was extracted using ethyl acetate (1:3, v/v) at pH 7.0. The separation of active ingredient and its purification was performed by using both thin layer chromatography (TLC) and column chromatography (CC) techniques. Spectrometric studies such as UV-visible, FTIR, and NMR and mass were performed. The antibacterial activity of pure compound was performed by cup plate method against some pathogenic bacteria including of streptomycin resistant bacteria like (Pseudomonas mirabilis, Pseudomonas putida and Bacillus cereus). In conclusion, the collected data emphasized the fact that a polypeptide antibiotic (Actinomycin D) was produced by Streptomyces parvulus RSPSN2.
从孟加拉湾维沙卡帕特南海岸的海洋土壤沉积物中分离出一株高产次级代谢产物的放线菌菌株。从采集的土壤沉积物中总共分离出了十株菌株。在这十株放线菌菌株中,选择了广谱菌株RSPSN2进行分子特征分析、抗生素生产及其纯化。最具活性的菌株的16S rRNA基因(1261个碱基对)的核苷酸序列显示与微小链霉菌1044菌株、微小链霉菌NBRC 13193和微小链霉菌BY-F有96%的相似性。从分类学特征来看,放线菌分离株RSPSN2在形态、生理和生化特征上与微小链霉菌匹配。因此,它被赋予了建议名称微小链霉菌RSPSN2。在pH 7.0条件下,使用乙酸乙酯(1:3,v/v)提取活性代谢产物。通过薄层色谱(TLC)和柱色谱(CC)技术进行活性成分的分离和纯化。进行了紫外可见光谱、傅里叶变换红外光谱、核磁共振和质谱等光谱研究。通过杯碟法对纯化合物对一些病原菌进行抗菌活性测试,包括对链霉素耐药菌(奇异变形杆菌、恶臭假单胞菌和蜡样芽孢杆菌)。总之,收集到的数据强调了微小链霉菌RSPSN2产生了一种多肽抗生素(放线菌素D)这一事实。