Two-step separation of nostotrebin 6 from cultivated soil cyanobacterium (Nostoc sp.) by high performance countercurrent chromatography
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24968333
PubMed Central
PMC6271089
DOI
10.3390/molecules19078773
PII: molecules19078773
Knihovny.cz E-zdroje
- MeSH
- acetáty chemie MeSH
- cholinesterasové inhibitory chemie izolace a purifikace MeSH
- cyklopentany chemie izolace a purifikace MeSH
- hexany chemie MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací MeSH
- methanol chemie MeSH
- Nostoc chemie MeSH
- protiproudá chromatografie MeSH
- půdní mikrobiologie MeSH
- rozpouštědla chemie MeSH
- voda chemie MeSH
- vysokoúčinná kapalinová chromatografie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetáty MeSH
- cholinesterasové inhibitory MeSH
- cyklopentany MeSH
- ethyl acetate MeSH Prohlížeč
- hexany MeSH
- methanol MeSH
- n-hexane MeSH Prohlížeč
- nostotrebin 6 MeSH Prohlížeč
- rozpouštědla MeSH
- voda 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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