Hesse Friedemann, Ebel Maria, Konisch Nadine, Sterlinski Reinhard, Kessler Wolfgang, Wagner Roland
German Research Centre for Biotechnology (GBF), Mascheroder Weg 1, D-38124 Braunschweig, Germany.
Biotechnol Prog. 2003 May-Jun;19(3):833-43. doi: 10.1021/bp0257630.
The applicability of a protein-free medium for the production of recombinant human interleukin-2 with baby hamster kidney cells in airlift bioreactors was investigated. For this purpose, a BHK-21 cell line, adapted to grow and produce in protein-free SMIF7 medium without forming spheroids in membrane-aerated bubble-free bioreactors, was used as the producer cell line. First, cultivation of the cells was established at a 20-L scale using an internal loop airlift bioreactor system. During the culturing process the medium formulation was optimized according to the specific requirements associated with cultivation of mammalian cells under protein-free conditions in a bubble-aerated system. The effects of the addition of an antifoam agent on growth, viability, productivity, metabolic rates, and release of lactate dehydrogenase were investigated. Although it was possible to establish cultivation and production at a 20-L scale without the use of antifoaming substances, the addition of 0.002% silicon-oil-based antifoaming reagent improved the cultivation system by completely preventing foam formation. This reduced the release of lactate dehydrogenase activity to the level found in bubble-free aerated stirred tank membrane bioreactors and led to a reduction in generation doubling times by about 5 h (17%). Using the optimized medium formulation, cells were cultivated at a 1000-L scale, resulting in a culture performance comparable to the 20-L airlift bioreactor. For comparison, cultivations with protein-containing SMIF7 medium were carried out at 20- and 1000-L scales. The application of protein supplements did not lead to a significant improvement in the cultivation conditions. The results were also compared with experiments performed in a bubble-free aerated stirred tank membrane bioreactor to evaluate the influence of bubbles on the investigated culture parameters. The data implied a higher metabolic activity of the cells in airlift bioreactors with a 150% higher glucose consumption rate. The results of this study clearly demonstrate the applicability of a protein-free chemically defined medium for the production of recombinant proteins with BHK cells in airlift bioreactors.
研究了无蛋白培养基在气升式生物反应器中用幼仓鼠肾细胞生产重组人白细胞介素-2的适用性。为此,使用了一种适应在无蛋白SMIF7培养基中生长和生产、且在膜曝气无泡生物反应器中不形成球体的BHK-21细胞系作为生产细胞系。首先,使用内部循环气升式生物反应器系统在20升规模上建立细胞培养。在培养过程中,根据在鼓泡曝气系统中无蛋白条件下培养哺乳动物细胞的特定要求,对培养基配方进行了优化。研究了添加消泡剂对生长、活力、生产力、代谢率和乳酸脱氢酶释放的影响。尽管不使用消泡物质也可以在20升规模上建立培养和生产,但添加0.002%的硅油基消泡剂通过完全防止泡沫形成改善了培养系统。这将乳酸脱氢酶活性的释放降低到无泡曝气搅拌罐膜生物反应器中的水平,并使世代倍增时间减少了约5小时(17%)。使用优化后的培养基配方,细胞在1000升规模上进行培养,培养性能与20升气升式生物反应器相当。为了进行比较,在20升和1000升规模上使用含蛋白的SMIF7培养基进行培养。添加蛋白质补充剂并未导致培养条件有显著改善。还将结果与在无泡曝气搅拌罐膜生物反应器中进行的实验进行了比较,以评估气泡对所研究培养参数的影响。数据表明气升式生物反应器中细胞的代谢活性更高,葡萄糖消耗率高出150%。这项研究的结果清楚地证明了无蛋白化学限定培养基在气升式生物反应器中用BHK细胞生产重组蛋白的适用性。