Microbial Biotechnology Division, CSIR-Indian Institute of Integrative Medicine, Jammu Tawi, India.
Academy of Scientific and Innovative Research, CSIR-Indian Institute of Integrative Medicine, Jammu Tawi, India.
J Appl Microbiol. 2020 May;128(5):1366-1377. doi: 10.1111/jam.14568. Epub 2020 Jan 16.
To evaluate the antimicrobial potential of Juglomycins isolated from Streptomyces achromogenes E91CS4, an endophyte of Crocus sativus Linn.
The extract from E91CS4 displayed significant antimicrobial activity against several pathogens. The endophyte was identified as S. achromogenes on by 16S ribosomal gene analysis. Chemical investigation of the extract led to the isolation of two naphthoquinone antibiotics, Juglomycin A and B. Juglomycin A inhibited several pathogens, with an MIC value of 13·7µg ml , whereas it was most potent against Escherichia coli, Bacillus thuringiensis and Xanthobacter flavus with MIC values of 6·8, 3·4 and 6·8 µg ml respectively. It was found to reduce the biofilm formation in E. coli through inhibition of swimming and swarming motilities and downregulation of fimH gene. The α-haemolysin-related gene (hlyA) was also downregulated indicating that the compound is also reducing the virulence in E. coli. In vitro time kill kinetics showed efficient bactericidal activity of this compound. Furthermore, Juglomycin A inhibited bacterial transcription/translation in vitro, while also inducing postantibiotic effect in E. coli.
Juglomycin A is a potential antimicrobial compound against several bacterial pathogens, particularly, E. coli.
This study showed the promising potential of Juglomycin A as an antimicrobial agent. Efforts should be made to scale up the production of this compound and conduct further studies to explore its efficacy as an antibiotic, using in vivo models.
评估从藏红花内生放线菌链霉菌 Achromogenes E91CS4 中分离得到的胡桃醌的抗菌潜力。
E91CS4 的提取物对几种病原体具有显著的抗菌活性。通过 16S 核糖体基因分析,内生菌被鉴定为 S. achromogenes。提取物的化学研究导致分离出两种萘醌抗生素,胡桃醌 A 和 B。胡桃醌 A 抑制了几种病原体,MIC 值为 13.7μg/ml,而对大肠杆菌、苏云金芽孢杆菌和黄单胞菌的抑菌活性最强,MIC 值分别为 6.8、3.4 和 6.8μg/ml。它通过抑制游泳和群集运动以及下调 fimH 基因来减少大肠杆菌中的生物膜形成。还发现 α-溶血素相关基因 (hlyA) 下调表明该化合物也降低了大肠杆菌的毒力。体外时间杀伤动力学显示该化合物具有有效的杀菌活性。此外,胡桃醌 A 抑制了大肠杆菌中的细菌转录/翻译,同时也诱导了其抗生素后效应。
胡桃醌 A 是一种对抗几种细菌病原体的潜在抗菌化合物,特别是大肠杆菌。
本研究表明胡桃醌 A 作为一种抗菌剂具有很大的潜力。应努力扩大该化合物的生产规模,并进一步研究其作为抗生素的功效,使用体内模型。