AVT - Biochemical Engineering, RWTH Aachen University, Forckenbeckstraße 51, Aachen 52074, Germany.
International R&D Laundry and Homecare, Henkel AG & Co KGaA, Henkelstr. 67, Düsseldorf 40589, Germany.
J Biosci Bioeng. 2019 Nov;128(5):599-605. doi: 10.1016/j.jbiosc.2019.05.003. Epub 2019 Jun 20.
Most industrial fermentation processes are operated in fed-batch mode to overcome catabolite repression, undesired by-product formation and oxygen limitation. To maintain comparable process conditions during screening of optimal production strains, the implementation of a fed-batch mode at small scale is crucial. In this study, three different protease producing Bacillus species, Bacillus aeolius, B. licheniformis and B. pumilus, were cultivated using the previously described membrane-based fed-batch shake flasks. Under carbon-limited conditions, catabolite repression was avoided, so that proteases were produced in all strains. Protease yields of B. aeolius and B. licheniformis increased 1.5-fold relative to batch cultivations. To validate process scalability between shake flasks and stirred tank reactors, membrane-based fed-batch shake flask cultivations were transferred to laboratory-scale stirred tank reactors with equal feeding rates. Despite inevitable differences between the scales such as pH control, feed supply and feed start, comparable results were achieved. Oxygen transfer rates of B. licheniformis and B. pumilus measured with the respiration activity monitoring system (RAMOS) in shake flasks and in stirred tank reactor with an off-gas analyzer were almost identical in both cultivation systems. The protease activities referring to the total consumed glucose were also mostly comparable. A slight decrease from shake flask to stirred tank reactor could be observed, which is presumably due to differences in pH control. This study successfully demonstrates the transferability of membrane-based fed-batch shake flask cultivations to laboratory-scale stirred tank reactors.
大多数工业发酵过程采用补料分批培养方式以克服分解代谢物抑制、不期望的副产物形成和氧限制。为了在筛选最佳生产菌株期间保持可比的过程条件,小规模实施补料分批培养方式至关重要。在这项研究中,使用先前描述的基于膜的补料分批摇瓶培养了三种不同的产蛋白酶芽孢杆菌,即解淀粉芽孢杆菌、地衣芽孢杆菌和短小芽孢杆菌。在碳限制条件下,避免了分解代谢物抑制,因此所有菌株都产生了蛋白酶。与分批培养相比,解淀粉芽孢杆菌和地衣芽孢杆菌的蛋白酶产量增加了 1.5 倍。为了验证摇瓶和搅拌罐反应器之间的过程可扩展性,将基于膜的补料分批摇瓶培养转移到具有相同进料率的实验室规模搅拌罐反应器中。尽管在 pH 控制、进料供应和进料开始等方面存在不可避免的规模差异,但仍获得了可比的结果。使用呼吸活性监测系统 (RAMOS) 在摇瓶和带有废气分析仪的搅拌罐反应器中测量的地衣芽孢杆菌和短小芽孢杆菌的氧传递速率在两种培养系统中几乎相同。参考总消耗葡萄糖的蛋白酶活性也大多相当。从摇瓶到搅拌罐反应器观察到略有下降,这可能是由于 pH 控制的差异所致。这项研究成功地证明了基于膜的补料分批摇瓶培养可以转移到实验室规模的搅拌罐反应器中。