抗菌剂
布鲁氏菌
生物信息学
传统医学
生物
植物化学
微生物学
布鲁氏菌
化学
生物化学
医学
病毒学
布鲁氏菌病
基因
作者
Ijaz Muhammad,Sadaf Niaz,Gul E Nayab,Anwar Hussain,Saghir Ahmad,Noor Rahman,Haroon Khan,Abid Ali
出处
期刊:Current Computer - Aided Drug Design
[Bentham Science Publishers]
日期:2020-06-13
卷期号:17 (7): 946-956
被引量:3
标识
DOI:10.2174/1573409916666200612145712
摘要
Brucellosis is an economically important zoonotic disease caused by the Gram-negative bacteria belonging to the genus Brucella. Medicinal plants are well known for a wide variety of potential antimicrobial agents that can be used as antimicrobial drugs.In the present study, crude ethanolic and methanolic extracts of local plants (Berberis lyceum and Fagonia cretica) were tested in vitro against Brucella melitensis via a well diffusion method for their antibacterial activity. In the in silico study, phytochemicals previously identified in the selected plants were docked with a homology model of the cytotoxic factor malate synthase G (MSG) highly conserved among Brucella spp., in Molecular Operating Environment (MOE) to predict a potential drug against B. melitensis. A molecular dynamic simulation was performed to predict the stability of MSG through MOE.Ethanolic crude extracts of B. lyceum showed maximum zone of inhibition (32.5 mm) followed by methanolic extracts (30 mm), while ethanolic extracts of F. cretica showed zone of inhibition (29 mm) followed by methanolic extracts (27.5 mm). In silico screening predicted phytic acid as the most potent inhibitor followed by jehlumine, barbamine, oxyberberine and sindamine.The synergistic utilization of phytochemicals derived from B. lyceum may potentially provide protection against B. melitensis.
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