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Zelkovamycins B-E, Cyclic Octapeptides Containing Rare Amino Acid Residues from an Endophytic Kitasatospora sp.

Xiaomeng HaoJiaqing YuYujia WangJack A ConnollyYufeng LiuYuqin ZhangLi-Yan YuShan CenRebecca J M GossMaoluo Gan
Published in: Organic letters (2020)
Four unusual cyclopeptides, zelkovamycins B-E (1-4), were isolated from an endophytic Kitasatospora sp. Zelkovamycin B was featured by an unprecedented 3-methyl-5-hydroxypyrrolidine-2,4-dione ring system linked to the cyclopeptide skeleton. Their structures and full configurations were established by spectroscopic analysis, Marfey's method, and NMR calculations. A plausible biosynthetic pathway for zelkovamycins was proposed based on gene cluster analysis. Zelkovamycin E displayed potent inhibitory activity against H1N1 influenza A virus.
Keyphrases
  • amino acid
  • high resolution
  • magnetic resonance
  • gene expression
  • molecular dynamics
  • molecular docking
  • dna methylation
  • genome wide
  • genome wide identification