Rajan Benita Mercy, Kannabiran Krishnan
Division of Biomolecules and Genetics, School of Biosciences and Technology, VIT University, India.
Int J Mol Cell Med. 2014 Summer;3(3):130-7.
Actinomycetes were isolated from marine sediment samples collected from the east coast of Chennai, Tamil Nadu, India. Well diffusion and agar plug methods were used for the evaluation of antibiotic production by these isolates against drug resistant Methicillin- resistant Staphylococcus aureus (MRSA) and vancomycin resistant Enterococci (VRE). The potential isolate VITBRK2 was mass cultured for morphological and physiological characterization. The culturing conditions of the isolate were optimized and the recommendations of International Streptomyces Project were followed for the assimilation of carbon and nitrogen sources. The isolate was identified by comparing the properties with representative species in the key of Nonomura and Bergey's Manual of Determinative Bacteriology. Ethyl acetate extract prepared from the cell free culture broth of the isolate was analyzed using HPLC- diode array technique to characterize the metabolites and identify the antibiotics. VITBRK2 was found to be Gram-positive rod grey color aerial mycelium production. It was also non motile in nature with spiral spore chain morphology. VITBRK2 was identified as Streptomyces and designated as Streptomyces sp. VITBRK2. HPLC-DAD analysis showed the presence of indolo compounds (3- methyl-indole and 2-methyl- indole) along with amicoumacin antibiotic. The observed activity of Streptomyces sp. VITBRK2 against MRSA and VRE strains may be due to the presence of indolo compounds in the isolate. The results of this study suggested that secondary metabolites produced by Streptomyces sp. VITBRK2 could be used as a lead to control drug resistant bacterial pathogens.
放线菌是从印度泰米尔纳德邦金奈东海岸采集的海洋沉积物样本中分离出来的。采用平板扩散法和琼脂块法评估这些分离株对耐甲氧西林金黄色葡萄球菌(MRSA)和耐万古霉素肠球菌(VRE)的抗生素产生情况。对潜在分离株VITBRK2进行大规模培养以进行形态学和生理学特征分析。优化了该分离株的培养条件,并遵循国际链霉菌项目的建议进行碳源和氮源的同化。通过将该分离株的特性与野村氏和《伯杰氏鉴定细菌学手册》中的代表性物种进行比较来鉴定该分离株。使用高效液相色谱 - 二极管阵列技术分析从该分离株的无细胞培养液中制备的乙酸乙酯提取物,以表征代谢产物并鉴定抗生素。发现VITBRK2为革兰氏阳性杆菌,产生灰色气生菌丝体。其在自然界中也不运动,具有螺旋状孢子链形态。VITBRK2被鉴定为链霉菌,并命名为链霉菌属VITBRK2。高效液相色谱 - 二极管阵列分析表明存在吲哚化合物(3 - 甲基吲哚和2 - 甲基吲哚)以及氨甲环素抗生素。观察到链霉菌属VITBRK2对MRSA和VRE菌株的活性可能归因于该分离株中存在吲哚化合物。本研究结果表明,链霉菌属VITBRK2产生的次生代谢产物可作为控制耐药细菌病原体的先导物。