A rare diketopiperazine glycoside from marine-sourced Streptomyces sp. ZZ446

Nat Prod Res. 2020 Apr;34(7):1046-1050. doi: 10.1080/14786419.2018.1544978. Epub 2018 Dec 22.

Abstract

Two diketopiperazines were isolated from a culture of the marine-derived actinomycete Streptomyces sp. ZZ446. Their structures were elucidated as maculosin (1) and maculosin-O-α-L-rhamnopyranoside (2) based on their NMR and HRESIMS data, specific rotation, and chemical degradation. Maculosin-O-α-L-rhamnopyranoside (2) is a new diketopiperazine glycoside, a structural class not reported previously from the natural sources. Both compounds showed antimicrobial activity against methicillin-resistant Staphylococcus aureus, Escherichia coli, and Candida albicans with MIC values in a range from 26.0 to 37.0 μg/mL.[Formula: see text].

Keywords: Streptomyces sp. ZZ446; antimicrobial activity; diketopiperazine glycoside.

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / isolation & purification
  • Candida albicans / drug effects
  • Diketopiperazines / chemistry
  • Diketopiperazines / isolation & purification*
  • Escherichia coli / drug effects
  • Glycosides / chemistry
  • Glycosides / isolation & purification*
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Peptides, Cyclic
  • Piperazines
  • Streptomyces / chemistry*

Substances

  • Anti-Bacterial Agents
  • Diketopiperazines
  • Glycosides
  • Peptides, Cyclic
  • Piperazines
  • maculosin