Production of Fucoxanthin from <i>Phaeodactylum tricornutum</i> Using High Performance Countercurrent Chromatography Retaining Its FOXO3 Nuclear Translocation-Inducing Effect
Daniela Bárcenas-Pérez,
Antonín Střížek,
Pavel Hrouzek,
Jiří Kopecký,
Marta Barradas,
Arantzazu Sierra-Ramirez,
Pablo J. Fernandez-Marcos,
José Cheel
Affiliations
Daniela Bárcenas-Pérez
Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický Mlýn, 379 81 Třeboň, Czech Republic
Antonín Střížek
Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický Mlýn, 379 81 Třeboň, Czech Republic
Pavel Hrouzek
Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický Mlýn, 379 81 Třeboň, Czech Republic
Jiří Kopecký
Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický Mlýn, 379 81 Třeboň, Czech Republic
Marta Barradas
Metabolic Syndrome Group—BIOPROMET, Madrid Institute for Advanced Studies—IMDEA Food, CEI UAM+CSIC, 28049 Madrid, Spain
Arantzazu Sierra-Ramirez
Metabolic Syndrome Group—BIOPROMET, Madrid Institute for Advanced Studies—IMDEA Food, CEI UAM+CSIC, 28049 Madrid, Spain
Pablo J. Fernandez-Marcos
Metabolic Syndrome Group—BIOPROMET, Madrid Institute for Advanced Studies—IMDEA Food, CEI UAM+CSIC, 28049 Madrid, Spain
José Cheel
Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický Mlýn, 379 81 Třeboň, Czech Republic
Phaeodactylum tricornutum is a rich source of fucoxanthin, a carotenoid with several health benefits. In the present study, high performance countercurrent chromatography (HPCCC) was used to isolate fucoxanthin from an extract of P. tricornutum. A multiple sequential injection HPCCC method was developed combining two elution modes (reverse phase and extrusion). The lower phase of a biphasic solvent system (n-heptane, ethyl acetate, ethanol and water, ratio 5/5/6/3, v/v/v/v) was used as the mobile phase, while the upper phase was the stationary phase. Ten consecutive sample injections (240 mg of extract each) were performed leading to the separation of 38 mg fucoxanthin with purity of 97% and a recovery of 98%. The process throughput was 0.189 g/h, while the efficiency per gram of fucoxanthin was 0.003 g/h. Environmental risk and general process evaluation factors were used for assessment of the developed separation method and compared with existing fucoxanthin liquid-liquid isolation methods. The isolated fucoxanthin retained its well-described ability to induce nuclear translocation of transcription factor FOXO3. Overall, the developed isolation method may represent a useful model to produce biologically active fucoxanthin from diatom biomass.