Trikoveramides A-C, cyclic depsipeptides from the marine cyanobacterium Symploca hydnoides

Phytochemistry. 2021 Oct:190:112879. doi: 10.1016/j.phytochem.2021.112879. Epub 2021 Jul 14.

Abstract

Trikoveramides A - C, members of the kulolide superfamily of cyclic depsipeptides, were isolated from the marine cyanobacterium, Symploca hydnoides, collected from Bintan Island, Indonesia. Their planar structures were elucidated by a combination of NMR spectroscopy and HRMS spectral data. The absolute configurations of the amino acid and phenyllactic acid units were confirmed by Marfey's and chiral HPLC analyses, respectively, while the relative stereochemistry of the 3-hydroxy-2-methyl-7-octynoic acid (Hmoya) unit in trikoveramide A was elucidated by the application of the J-based configuration analysis and NOE correlations. The cytotoxic activity of the trikoveramides were evaluated against MOLT-4 human leukemia cells and gave IC50 values of 9.3 μM, 35.6 μM and 48.8 μM for trikoveramide B, trikoveramide C and trikoveramide A, respectively. In addition, trikoveramides A - C showed weak to moderate inhibition in the quorum sensing inhibitory assay based on the Pseudomonas aeruginosa lasB-gfp and rhlA-gfp bioreporter strains.

Keywords: Cyclic depsipeptides; Kulolide superfamily; Microcoleaceae; Symploca hydnoides; Trikoveramides.

MeSH terms

  • Cyanobacteria*
  • Depsipeptides* / pharmacology
  • Drug Screening Assays, Antitumor
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptides, Cyclic

Substances

  • Depsipeptides
  • Peptides, Cyclic

Supplementary concepts

  • Symploca hydnoides