Mehravar Maryam, Sardari Soroush, Owlia Parviz
Drug Design and Bioinformatics Unit, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran #69 Pasteur Ave.,Tehran, 13164, Iran.
Indian J Exp Biol. 2011 Dec;49(12):946-52.
Increased resistance of pathogens toward existing antibiotics has compelled the research efforts to introduce new antimicrobial substances. Drugs with new and less resistant-prone targets to antimicrobial activity have a high priority for drug development activities. Cell membrane seems to be a potential target for new antibiotic agent development to overcome resistance. In this study, A total number of 67 actinomycetes were isolated from the soil samples collected from desert, farming and mineral parts of Iran. We used a chromatic sensor as a membrane model that was set up for the target of antimicrobial metabolites of actinomycetes isolated from the soil. The sensors particles were composed of phospholipid and polymerized polydiacetylene (PDA) lipids. These polymers exhibited color change following interaction with membrane-active metabolites. The color change was due to structural disorder in the lipids following their interaction with membrane-active metabolites. The resultant color change was recorded by fluorescent microscope and easily recognizable by naked eye as well. Sixteen strains were isolated which produced antimicrobial metabolites and were effective against test microorganisms (Escherichia coli, Candida albicans and Saccharomyces cerevisiae ). A total number of 3 out of 16 strains produced membrane-active metabolites. These 3 strains were identified using 16s rRNA as Streptomyces sp and submitted to GenBank (accession no. JN180853; JN180854; JN180855).
病原体对现有抗生素的耐药性增加,促使人们开展研究以引入新的抗菌物质。对抗菌活性具有新的且不易产生耐药性靶点的药物在药物研发活动中具有高度优先性。细胞膜似乎是开发新型抗生素以克服耐药性的潜在靶点。在本研究中,从伊朗沙漠、农田和矿区采集的土壤样本中总共分离出67株放线菌。我们使用一种彩色传感器作为膜模型,该模型用于针对从土壤中分离出的放线菌抗菌代谢物的靶点。传感器颗粒由磷脂和聚合聚二乙炔(PDA)脂质组成。这些聚合物在与膜活性代谢物相互作用后会发生颜色变化。颜色变化是由于脂质与膜活性代谢物相互作用后其结构紊乱所致。由此产生的颜色变化通过荧光显微镜记录,肉眼也很容易识别。分离出16株产生抗菌代谢物且对测试微生物(大肠杆菌、白色念珠菌和酿酒酵母)有效的菌株。16株菌株中共有3株产生膜活性代谢物。这3株菌株通过16s rRNA鉴定为链霉菌属,并提交至GenBank(登录号:JN180853;JN180854;JN180855)。