Arumugam T, Senthil Kumar P, Kameshwar R, Prapanchana K
Department of Chemical Engineering, SSN College of Engineering, Kalavakkam, Chennai, 603 110, India.
Department of Chemical Engineering, SSN College of Engineering, Kalavakkam, Chennai, 603 110, India.
Microb Pathog. 2017 Jun;107:225-233. doi: 10.1016/j.micpath.2017.03.035. Epub 2017 Mar 30.
The importance of the current research is to investigate the different types of samples from the various mangrove sediments; as source of actinobacteria from the mangrove wet soil. Potential isolate screening by antimicrobial activity and identified actinobacteria was characterized based on cultural morphology, physiological and biochemical characteristics. Three different types of media were used to isolate actinobacteria from various geographical region of mangrove soil sediment and the genotype locus was recognized by 16S rDNA. Totally 144 actinobacteria isolates were recovered from 10 samples using three media. The most active culture media in the isolation of actinobacteria were ISP2 and Glycerol Yeast Extract Agar. Among 144 isolates, 38 isolates (26.38%) exhibited antimicrobial activity. Out of 38 isolates, potentially active 2 cultures were further supported for morphological and biochemical characterization analysis. Most of the isolates were produced pharmaceutically important enzymes such as protease, amylase, lipase, cellulose and also revealed antimicrobial activity against tested microorganism. The enriched salt, pH and temperature tolerance of the actinobacteria isolates to discharge commercially valuable primary and secondary bioactive metabolites. The present results functionally characterize novel mangrove actinobacteria and their metabolites for commercial interest in pharmaceutical industry.
当前研究的重要性在于调查来自各种红树林沉积物的不同类型样本;作为红树林湿地土壤中放线菌的来源。通过抗菌活性进行潜在分离株筛选,并基于培养形态、生理和生化特征对鉴定出的放线菌进行表征。使用三种不同类型的培养基从红树林土壤沉积物的不同地理区域分离放线菌,并通过16S rDNA识别基因型位点。使用三种培养基从10个样本中共回收了144株放线菌分离株。在放线菌分离中最活跃的培养基是ISP2和甘油酵母提取物琼脂。在144株分离株中,38株(26.38%)表现出抗菌活性。在38株分离株中,对2株潜在活性培养物进一步进行形态和生化表征分析。大多数分离株产生了具有药学重要性的酶,如蛋白酶、淀粉酶、脂肪酶、纤维素酶,并且还对测试微生物显示出抗菌活性。放线菌分离株对盐、pH和温度的耐受性增强,可释放具有商业价值的初级和次级生物活性代谢产物。目前的结果从功能上表征了新型红树林放线菌及其代谢产物,以满足制药行业的商业利益。