Two-step separation of nostotrebin 6 from cultivated soil cyanobacterium (Nostoc sp.) by high performance countercurrent chromatography
Language English Country Switzerland Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24968333
PubMed Central
PMC6271089
DOI
10.3390/molecules19078773
PII: molecules19078773
Knihovny.cz E-resources
- MeSH
- Acetates chemistry MeSH
- Cholinesterase Inhibitors chemistry isolation & purification MeSH
- Cyclopentanes chemistry isolation & purification MeSH
- Hexanes chemistry MeSH
- Spectrometry, Mass, Electrospray Ionization MeSH
- Methanol chemistry MeSH
- Nostoc chemistry MeSH
- Countercurrent Distribution MeSH
- Soil Microbiology MeSH
- Solvents chemistry MeSH
- Water chemistry MeSH
- Chromatography, High Pressure Liquid MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acetates MeSH
- Cholinesterase Inhibitors MeSH
- Cyclopentanes MeSH
- ethyl acetate MeSH Browser
- Hexanes MeSH
- Methanol MeSH
- n-hexane MeSH Browser
- nostotrebin 6 MeSH Browser
- Solvents MeSH
- Water MeSH
High performance countercurrent chromatography (HPCCC) was successfully applied for the separation of nostotrebin 6 from cultivated soil cyanobacteria in a two-step operation. A two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (4:5:4:5, v/v/v/v) was employed for the HPCCC separation. In the first-step operation, its neutral upper phase was used as stationary phase and its basic lower phase (1% NH3 in lower phase) was employed as mobile phase at a flow rate of 1 mL/min. In the second operation step, its neutral upper phase was used as stationary phase, whereas both its neutral lower phase and basic lower phase were employed as mobile phase with a linear gradient elution at a flow rate of 0.8 mL/min. The revolution speed and temperature of the separation column were 1,000 rpm and 30 °C, respectively. Using HPCCC followed by clean-up on Sephadex LH-20 gel, 4 mg of nostotrebin 6 with a purity of 99% as determined by HPLC/DAD-ESI-HRMS was obtained from 100 mg of crude extract. The chemical identity of the isolated compound was confirmed by comparing its spectroscopic data (UV, ESI-HRMS, ESI-HRMS2) with those of an authentic standard and data available in the literature.
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