Open-loop control of the biomass concentration within the growth phase of recombinant protein production processes

被引:61
作者
Jenzsch, Marco
Gnoth, Stefan
Beck, Matthias
Kleinschmidt, Martin
Simutis, Rimvydas
Luebbert, Andreas
机构
[1] Univ Halle Wittenberg, Ctr Bioproc Engn, D-06120 Halle, Germany
[2] Probiodrug AG, D-06120 Halle, Germany
[3] Kaunas Univ Technol, Inst Automat & Control Technol, LT-3028 Kaunas, Lithuania
关键词
open-loop control; PAT; reproducible recombinant protein production; statistical process analysis;
D O I
10.1016/j.jbiotec.2006.06.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recombinant protein production processes are typically divided into two phases. In the first one, pure cell propagation takes place, while in the second one product formation is switched on within the cells by adding an inducer. In the initial biomass formation phase, the cell density is rather low and, hence, the measurement quantities that could be used to determine the process' state depict small values and are rather severely distorted by measurement noise. Because of these measurement problems, the fermentation cannot be reliably controlled by feedback control during this first production phase; instead, the process must be controlled in an open-loop fashion. The consequence, worked out in this paper, is to design substrate feed rate profiles for the growth phase in such a way that they are robust with respect to the main disturbances observed in practice. The robustness of the biomass formation is shown to be primarily dependent on the specific growth rate adjusted in the first hours. High batch-to-batch reproducibility can be obtained with exponential feeding profiles F(t) corresponding to specific growth rates mu(set) well below the maximal specific growth rate mu(max) of the organism. The reduction in the growth rate needed to obtain a robust process behavior depends on the inaccuracies in the initial biomass concentrations. Quantitative feed rate profiles were obtained by numerical simulation and these results were validated experimentally by means of a series of cultivation runs, where a recombinant pharmaceutical protein was produced. All experimental data confirmed the assumptions made in the robust process design study. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 94
页数:11
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