Steiner KayLee K, Parthasarathy Anutthaman, Wong Narayan H, Cavanaugh Nicole T, Chu Jonathan, Hudson André O
Thomas H. Gosnell School of Life Sciences, Rochester Institute of Technology, 85 Lomb Memorial Drive, Rochester, NY, 14623, USA.
BMC Res Notes. 2020 Aug 3;13(1):370. doi: 10.1186/s13104-020-05216-w.
There is an urgent need for the discovery and/or development of novel antibiotics. We report an exploration of "slow"-growing bacteria, which can be difficult to isolate using rich media as they are usually outcompeted by "fast"-growing bacteria, as potential sources of novel antimicrobials.
Pseudomonas sp. RIT 623 was isolated using pond water agar from a pond located on the campus of the Rochester Institute of Technology (RIT). The genome was sequenced and analyzed for potential secondary metabolite gene clusters. Bioinformatics analysis revealed 14 putative gene clusters predicted to encode pathways for the anabolism of secondary metabolites. Ethyl acetate extracts from spent growth medium of Pseudomonas sp. RIT 623 were tested against two Gram-negative (E. coli ATCC 25922 and P. aeruginosa ATCC 27853) and two Gram-positive (B. subtilis BGSC 168 and S. aureus ATCC 25923) type strains to assess antibiotic activity. The antibiotic assays demonstrated that extracts of Pseudomonas sp. RIT 623 were able to inhibit the growth of the four strains. The active compound was separated using diethyl ether in a multi-solvent extraction and reverse phase chromatography. The bioactive compound/s were subsequently eluted in two consecutive fractions corresponding to approximately 16-22% acetonitrile, indicative of polar compound/s.
迫切需要发现和/或开发新型抗生素。我们报告了对“生长缓慢”细菌的探索,这类细菌使用丰富培养基时可能难以分离,因为它们通常会被“生长快速”的细菌竞争淘汰,我们将其作为新型抗菌剂的潜在来源进行研究。
假单胞菌属RIT 623是从罗切斯特理工学院(RIT)校园内一个池塘的池塘水琼脂中分离出来的。对其基因组进行了测序,并分析了潜在的次级代谢产物基因簇。生物信息学分析揭示了14个推测的基因簇,预计这些基因簇编码次级代谢产物生物合成途径。对假单胞菌属RIT 623的废生长培养基的乙酸乙酯提取物针对两种革兰氏阴性菌(大肠杆菌ATCC 25922和铜绿假单胞菌ATCC 27853)和两种革兰氏阳性菌(枯草芽孢杆菌BGSC 168和金黄色葡萄球菌ATCC 25923)标准菌株进行测试,以评估抗生素活性。抗生素检测表明,假单胞菌属RIT 623的提取物能够抑制这四种菌株的生长。使用乙醚在多溶剂萃取和反相色谱中分离活性化合物。随后,生物活性化合物在两个连续的馏分中洗脱,对应于约16 - 22%的乙腈,表明是极性化合物。