4.7 Article

An antibacterial from Hypericum acmosepalum inhibits ATP-dependent MurE ligase from Mycobacterium tuberculosis

Journal

INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
Volume 39, Issue 2, Pages 124-129

Publisher

ELSEVIER
DOI: 10.1016/j.ijantimicag.2011.09.018

Keywords

Hypericum acmosepalum; Hyperenone A; Hypercalin B; Staphylococcus aureus; Tuberculosis; Peptidoglycan; MurE ligase

Funding

  1. UK Medical Research Council (MRC, UK) [GO801956]
  2. UNESCO-L'OREAL
  3. MRC [G0802079, G0801956] Funding Source: UKRI
  4. Medical Research Council [G0801956, G0802079] Funding Source: researchfish

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In a project to characterise new antibacterial chemotypes from plants, hyperenone A and hypercalin B were isolated from the hexane and chloroform extracts of the aerial parts of Hypericum acmosepalum. The structures of both compounds were characterised by extensive one-and two-dimensional nuclear magnetic resonance (NMR) spectroscopy and were confirmed by mass spectrometry. Hyperenone A and hypercalin B exhibited antibacterial activity against multidrug-resistant strains of Staphylococcus aureus, with minimum inhibition concentration ranges of 2-128 mg/L and 0.5-128 mg/L, respectively. Hyperenone A also showed growth-inhibitory activity against Mycobacterium tuberculosis H37Rv and Mycobacterium bovis BCG at 75 mg/L and 100 mg/L. Neither hyperenone A nor hypercalin B inhibited the growth of Escherichia coli and both were non-toxic to cultured mammalian macrophage cells. Both compounds were tested for their ability to inhibit the ATP-dependent MurE ligase of M. tuberculosis, a crucial enzyme in the cytoplasmic steps of peptidoglycan biosynthesis. Hyperenone A inhibited MurE selectively, whereas hypercalin B did not have any effect on enzyme activity. (C) 2011 Elsevier B. V. and the International Society of Chemotherapy. All rights reserved.

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