| Literature DB >> 29458855 |
Aehtesham Hussain1, Muzafar Ahmad Rather2, Mohd Saleem Dar3, N A Dangroo4, Mushtaq A Aga4, Arem Qayum3, Aabid Manzoor Shah5, Zahoor Ahmad2, Mohd Jamal Dar3, Qazi Parvaiz Hassan6.
Abstract
A highly active actinobacterial strain isolated from untapped areas of Northwestern Himalayas and characterised as Streptomyces puniceus strain AS13 by 16S rRNA gene sequencing was selected for production of bioactive metabolites. The bioassay-guided fractionation of microbial cultured ethyl acetate extract of the strain, led to isolation of macrotetrolide compound 1 (Dinactin) and compound 2 (1-(2,4-dihydroxy-6-methylphenyl)-ethanone). Structures of the isolated compounds were elucidated by [corrected] interpretation of NMR and other spectroscopic data including HR-ESI-MS, FT-IR. These compounds are reported for first time from Streptomyces Puniceus. Compound 1 exhibited strong anti-microbial activity against all tested bacterial pathogens including Mycobacterium tuberculosis. The MIC values of compound 1 against Gram negative and Gram positive bacterial pathogens ranged between 0.019 - 0.156μgml-1 and 1μgml-1 against Mycobacterium tuberculosis H37Rv. Dinactin exhibited marked anti-tumor potential with IC50 of 1.1- 9.7μM in various human cancerous cell lines and showed least cytotoxicity (IC50∼80μM) in normal cells (HEK-293). Dinactin inhabited cellular proliferation in cancer cells, reduced their clonogenic survival as validated by clonogenic assay and also inhabited cell migration and invasion characteristics in colon cancer (HCT-116) cells. Our results expressed the antimicrobial potential of dinactin and also spotted its prospective as an antitumor antibiotic.Entities:
Keywords: Actinomycetes; Antitumor antibiotic; Bioactive metabolites; Fermentation; Streptomyces puniceus
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Year: 2017 PMID: 29458855 DOI: 10.1016/j.micres.2017.12.004
Source DB: PubMed Journal: Microbiol Res ISSN: 0944-5013 Impact factor: 5.415