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Genome mining of actinomycin shunt products from Kitasatospora sp. YINM00002.

Zhou-Tian-Le ZhangHui-Bing SunZhen RenTian-Peng XieYing-Fang WangYin GuoXiaoyu SuMin YinHao ZhouZhong-Tao Ding
Published in: RSC advances (2023)
Actinomycins are known for their anti-tumor, antibacterial and antiviral activities, and in particular for the ability of actinomycin D as a clinical drug to treat a variety of cancers. In our ongoing work to obtain novel natural products from endophytic actinomycetes derived from traditional Chinese herbs, we identified the potential to produce actinomycins in YINM00002, a Kitasatospora strain derived from Polygonatum kingianum . According to genome mining, we isolated actinomycins D and V (1 and 2) and small amounts of 4-methyl-3-hydroxyanthranilic acid (4-MHA) derivates (3 and 4) from strain fermentation broth. The presence of actinrhater A (3) and actinrhater B (4) reveals a mysterious shunt pathway in the early stages of actinomycin D biosynthesis. Our study provides a fresh perspective for further discovery and modification of novel actinomycins.
Keyphrases
  • pulmonary artery
  • genome wide
  • small molecule
  • high throughput
  • dna methylation
  • human health
  • saccharomyces cerevisiae
  • anti inflammatory
  • single cell
  • wound healing
  • adverse drug
  • cell wall
  • lactic acid