Bauer S, White M D
Biotechnol Bioeng. 1976 Jun;18(6):839-46. doi: 10.1002/bit.260180606.
An efficient method to grow Escherichia coli W to high cell concentrations on the pilot scale is described and discussed. The method involves growth linked introduction of glucose and ammonia to the culture, sparging with oxygen, and maintenance of aerobic conditions by gradually decreasing the temperature in the culture in order to keep the oxygen demand within the limits of the capacity of supply. Under these conditions the linear rate of cell mass production is actually the result of exponential growth with a gradually decreasing growth-rate constant. About 10 kg packed cells were produced in a 50 liter working-volume fermentor in one run of 13 hr. The concentration of the cells at the end of the growth was about 47 g dry cells/liter. The expenditure for nutrients was minimal and the controls were of simple automatic nature. From the determined yield constants for glucose, nitrogen, phosphorus, and oxygen it may be inferred that the cells grown by this method are similar to those grown exponentially at constant temperature.
本文描述并讨论了一种在中试规模下将大肠杆菌W培养至高细胞浓度的有效方法。该方法包括将葡萄糖和氨与培养过程相联系地引入、用氧气鼓泡以及通过逐渐降低培养温度来维持有氧条件,以便将氧气需求保持在供应能力范围内。在这些条件下,细胞质量的线性生产速率实际上是生长速率常数逐渐降低的指数生长的结果。在一个13小时的运行过程中,一个50升工作体积的发酵罐中生产了约10千克的堆积细胞。生长结束时细胞浓度约为47克干细胞/升。营养物质的消耗极少,且控制是简单的自动性质。从所测定的葡萄糖、氮、磷和氧气的产率常数可以推断,用这种方法培养的细胞与在恒温下指数生长的细胞相似。