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Bioreactor seaweed cell culture for production of bioactive oxylipins
Authors:G. L. Rorrer  J. Modrell  C. Zhi  H. -D. Yoo  D. N. Nagle  W. H. Gerwick
Affiliation:(1) Department of Chemical Engineering, Oregon State University, 97331 Corvallis, OR, USA;(2) College of Pharmacy, Oregon State University, 97331 Corvallis, OR, USA
Abstract:Liquid cell suspension cultures derived from marine plants have the potential to biosynthesize novel biomedicinal compounds in a controlled environment. Of particular interest are the eicosanoids and related oxylipins emanating from the 15-lipoxygenase manifold of the arachidonic acid cascade, which is active in the brown algaLaminaria saccharina. Filamentous cell clumps ofL. saccharina isolated from female gametophytes were cultured in an illuminated bubble-column bioreactor in GP2 artificial seawater nutrient medium at 13 °C and air flow rate of 0.35 L air min–1 L–1 culture (vvm). Growth kinetics and biomass productivity data were obtained as a function of incident light intensity (2.4 to 98mgrmol photon m–2 s–1) and initial cell density (27 to 149 mg DCW L–1). Maximum cell densities exceeded 1200 mg DCW L–1 after a 20 day cultivation time at optimal conditions of 98mgrmol photon m–2 s–1 and 118 mg DCW L–1 initial cell density. Qualitative analysis of chloroform/methanol extracts of the cell culture biomass by GC-MS confirmed the presence of the hydroxy fatty acids 13-HODTA and 13-HOTE, the likely products of 15-lipoxygenase catalyzed oxidation of linoleic or linolenic acids.
Keywords:algal cell culture  bioreactor  hydroxy fatty acids
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