New Metabolites and Bioactive Actinomycins from Marine-Derived Streptomyces sp. ZZ338

Mar Drugs. 2016 Oct 11;14(10):181. doi: 10.3390/md14100181.

Abstract

An extract prepared from the culture of a marine-derived actinomycete Streptomyces sp. ZZ338 was found to have significant antimicrobial and antiproliferative activities. A chemical investigation of this active extract resulted in the isolation of three known bioactive actinomycins (1-3) and two new metabolites (4 and 5). The structures of the isolated compounds were identified as actinomycins D (1), V (2), X (3), 2-acetylamino-3-hydroxyl-4-methyl-benzoic acid methyl ester (4), and N-1S-(4-methylaminophenylmethyl)-2-oxo-propyl acetamide (5) based on their nuclear magnetic resonance (NMR) and high resolution electrospray ionization mass spectroscopy (HRESIMS) data as well as their optical rotation. This class of new compound 5 had never before been found from a natural resource. Three known actinomycins showed activities in inhibiting the proliferation of glioma cells and the growth of methicillin-resistant Staphylococcus aureus, Escherichia coli, and Candida albicans and are responsible for the activity of the crude extract. Actinomycin D (1) was also found to downregulate several glioma metabolic enzymes of glycolysis, glutaminolysis, and lipogenesis, suggesting that targeting multiple tumor metabolic regulators might be a new anti-glioma mechanism of actinomycin D. This is the first report of such a possible mechanism for the class of actinomycins.

Keywords: actinomycins; antimicrobial activity; antiproliferative activity; glioma cells; glioma metabolic enzymes; marine Streptomyces sp. ZZ338; new metabolites.

MeSH terms

  • Animals
  • Anti-Infective Agents / chemistry*
  • Anti-Infective Agents / pharmacology
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Candida albicans / drug effects
  • Dactinomycin / metabolism*
  • Dactinomycin / pharmacology
  • Drug Screening Assays, Antitumor
  • Escherichia coli / drug effects
  • Humans
  • Inhibitory Concentration 50
  • Oceans and Seas
  • Rats
  • Staphylococcus aureus / drug effects
  • Streptomyces / metabolism*
  • Structure-Activity Relationship
  • Tumor Cells, Cultured / drug effects

Substances

  • Anti-Infective Agents
  • Antineoplastic Agents
  • Dactinomycin