4.6 Article

Heterologous Expression in Anabaena of the Columbamide Pathway from the Cyanobacterium Moorena bouillonii and Production of New Analogs

Journal

ACS CHEMICAL BIOLOGY
Volume 17, Issue 7, Pages 1910-1923

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acschembio.2c00347

Keywords

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Funding

  1. National Institute of General Medical Sciences of the U.S. National Institutes of Health [R01GM118815, GBMF7622]
  2. Midwestern University One Health Initiative Funds
  3. Gordon and Betty Moore Foundation [GBMF7622]
  4. U.S. National Institutes of Health for the Center [P41GM103484]
  5. U.S. Department of Energy [DE-SC0021340, 1070261-436503]
  6. U.S. Department of Energy (DOE) [DE-SC0021340] Funding Source: U.S. Department of Energy (DOE)

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This study reports the heterologous expression of the columbamide biosynthetic gene cluster (BGC) in Anabaena, which encodes for the synthesis of columbamides. Several new columbamide analogs were identified using LC-MS/MS and NMR. The production of columbamides in Anabaena was found to be influenced by culture conditions, particularly the concentration of NaCl.
Columbamides are chlorinated acyl amide natural products, several of which exhibit cannabinomimetic activity. These compounds were originally discovered from a culture of the filamentous marine cyanobacterium Moorena bouillonii PNG5-198 collected from the coastal waters of Papua New Guinea. The columbamide biosynthetic gene cluster (BGC) had been identified using bioinformatics, but not confirmed by experimental evidence. Here, we report the heterologous expression in Anabaena (Nostoc) PCC 7120 of the 28.5 kb BGC that encodes for columbamide biosynthesis. The production of columbamides in Anabaena is investigated under several different culture conditions, and several new columbamide analogs are identified by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and nuclear magnetic resonance (NMR). In addition to previously characterized columbamides A, B, and C, new columbamides I-M are produced in these experiments, and the structure of the most abundant monochlorinated analog, columbamide K (11), is fully characterized. The other new columbamide analogs are produced in only small quantities, and structures are proposed based on high-resolution-MS, MS/MS, and 1H NMR data. Overexpression of the pathway's predicted halogenases resulted in increased productions of di-and trichlorinated compounds. The most significant change in production of columbamides in Anabaena is correlated with the concentration of NaCl in the medium.

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