Lowe K C, Anthony P, Davey M R, Power J B, Washington C
Department of Life Science, University of Nottingham, University Park, U.K.
Artif Cells Blood Substit Immobil Biotechnol. 1995;23(3):417-22. doi: 10.3109/10731199509117957.
Protoplasts isolated from cell suspensions of albino Petunia hybrida were grown for 10 d at the interface between aqueous culture medium and oxygenated perfluorodecalin. Protoplasts synthesised new cell walls and divided normally at the fluorocarbon/culture medium interface, the mean division frequency of protoplasts being increased by 37% (P < 0.05) in this system when the perfluorodecalin was saturated with oxygen prior to use. The mean division frequency of protoplasts was further increased to a maximum of 52% above control (P < 0.01) when the medium overlaying the oxygenated perfluorodecalin was supplemented with 0.01% (w/v) of the co-polymer surfactant, Pluronic F-68. These results demonstrate a beneficial and synergistic effect of supplementing protoplast culture systems with oxygenated perfluorodecalin and Pluronic F-68.
从白花矮牵牛细胞悬浮液中分离出的原生质体,在水培培养基与充氧全氟萘烷的界面处培养10天。原生质体在氟碳/培养基界面合成新细胞壁并正常分裂,当使用前全氟萘烷用氧气饱和时,该系统中原生质体的平均分裂频率提高了37%(P < 0.05)。当覆盖充氧全氟萘烷的培养基补充0.01%(w/v)的共聚物表面活性剂普朗尼克F - 68时,原生质体的平均分裂频率进一步提高,最高比对照增加52%(P < 0.01)。这些结果表明,用充氧全氟萘烷和普朗尼克F - 68补充原生质体培养系统具有有益的协同效应。