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Heterologous Production of the C33-C45 Polyketide Fragment of Anticancer Apratoxins in a Cyanobacterial Host.

Dipesh DhakalDimitris KallifidasManyun ChenSofia KokkaliariQi-Yin ChenValerie J PaulYousong DingHendrik Luesch
Published in: Organic letters (2023)
A polyketide synthase subcluster of cytotoxic apratoxin A was isolated from a Moorena bouillonii environmental DNA library and engineered with a thioesterase II domain for heterologous expression in the filamentous cyanobacterium Anabaena sp. PCC7120. Further engineering with a rhamnose-inducible promoter led to the production of (2 R ,3 R ,5 R ,7 R )-3,7-dihydroxy-2,5,8,8-tetramethylnonanoic acid, a stereogenically rich chiral building block that is important to the efficient synthesis of apratoxin analogues, representing the first synthetic biology attempt for this type of polyketide fragment.
Keyphrases
  • poor prognosis
  • dna methylation
  • saccharomyces cerevisiae
  • transcription factor
  • gene expression
  • circulating tumor
  • cell free
  • single molecule
  • human health
  • capillary electrophoresis
  • nucleic acid