Calothrixamides A and B from the Cultured Cyanobacterium Calothrix sp. UIC 10520.
Camila M CrnkovicAleksej KrunicDaniel S MayTyler A WilsonDiana KaoJoanna E BurdetteJoanna E BurdetteNicholas H OberliesJimmy E OrjalaPublished in: Journal of natural products (2018)
Cyanobacteria are a source of chemically diverse metabolites with potential medicinal and biotechnological applications. Rapid identification of compounds is central to expedite the natural product discovery process. Mass spectrometry has been shown to be an important tool for dereplication of complex natural product samples. In addition, chromatographic separation and complementary spectroscopic analysis (e.g., UV) can enhance the confidence of the dereplication process. Here, we applied a droplet-liquid microjunction-surface sampling probe (droplet probe) coupled with UPLC-PDA-HRMS-MS/MS to identify two new natural products in situ from the freshwater strain Calothrix sp. UIC 10520. This allowed us to prioritize this strain for chemical investigation based on the presence of new metabolites very early in our discovery process, saving both time and resources. Subsequently, calothrixamides A (1) and B (2) were isolated from large-scale cultures, and the structures were elucidated by 1D and 2D NMR spectroscopy and mass spectrometry. The absolute configurations were determined by a combination of chemical degradation reactions, derivatization methods (Mosher's, Marfey's, and phenylglycine methyl ester), and J-based configurational analysis. Calothrixamides showed no cytotoxic activity against the MDA-MB-435, MDA-MB-231, and OVCAR3 cancer cell lines. They represent the first functionalized long-chain fatty acid amides reported from the Calothrix genus and from a freshwater cyanobacterium.
Keyphrases
- ms ms
- mass spectrometry
- liquid chromatography
- high throughput
- high performance liquid chromatography
- simultaneous determination
- quantum dots
- small molecule
- fatty acid
- high resolution mass spectrometry
- gas chromatography
- high resolution
- breast cancer cells
- single cell
- liquid chromatography tandem mass spectrometry
- tandem mass spectrometry
- squamous cell carcinoma
- living cells
- endothelial cells
- molecular docking
- young adults
- ionic liquid
- risk assessment
- cell cycle arrest
- gas chromatography mass spectrometry
- squamous cell
- loop mediated isothermal amplification
- drug discovery