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  • 标题:Isolation, characterization, anti-MRSA evaluation, and in-silico multi-target anti-microbial validations of actinomycin X 2 and actinomycin D produced by novel Streptomyces smyrnaeus UKAQ_23
  • 本地全文:下载
  • 作者:Kamal A. Qureshi ; Avinash D. Bholay ; Pankaj K. Rai
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2021
  • 卷号:11
  • DOI:10.1038/s41598-021-93285-7
  • 语种:English
  • 出版社:Springer Nature
  • 摘要:Streptomyces smyrnaeus UKAQ_23, isolated from the mangrove-sediment, collected from Jubail,Saudi Arabia, exhibited substantial antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA), including non-MRSA Gram-positive test bacteria. The novel isolate, under laboratory-scale conditions, produced the highest yield (561.3 ± 0.3 mg/kg fermented agar) of antimicrobial compounds in modified ISP-4 agar at pH 6.5, temperature 35 °C, inoculum 5% v/w, agar 1.5% w/v, and an incubation period of 7 days. The two major compounds, K 1 and K 2, were isolated from fermented medium and identified as Actinomycin X 2 and Actinomycin D, respectively, based on their structural analysis. The antimicrobial screening showed that Actinomycin X 2 had the highest antimicrobial activity compared to Actinomycin D, and the actinomycins-mixture (X 2:D, 1:1, w/w) against MRSA and non-MRSA Gram-positive test bacteria, at 5 µg/disc concentrations. The MIC of Actinomycin X 2 ranged from 1.56–12.5 µg/ml for non-MRSA and 3.125–12.5 µg/ml for MRSA test bacteria. An in-silico molecular docking demonstrated isoleucyl tRNA synthetase as the most-favored antimicrobial protein target for both actinomycins, X 2 and D, while the penicillin-binding protein-1a, was the least-favorable target-protein. In conclusion, Streptomyces smyrnaeus UKAQ_23 emerged as a promising source of Actinomycin X 2 with the potential to be scaled up for industrial production, which could benefit the pharmaceutical industry.
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