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基因工程改造大肠杆菌中的产物形成动力学:包涵体形成

Product formation kinetics in genetically modified E. coli bacteria: inclusion body formation.

作者信息

Gnoth Stefan, Jenzsch Marco, Simutis Rimvydas, Lübbert Andreas

机构信息

Center of Bioprocess Engineering, Martin-Luther-University Halle-Wittenberg, 06120 Halle/Saale, Germany.

出版信息

Bioprocess Biosyst Eng. 2008 Jan;31(1):41-6. doi: 10.1007/s00449-007-0161-9. Epub 2007 Oct 10.

Abstract

A data-driven model is presented that can serve two important purposes. First, the specific growth rate and the specific product formation rate are determined as a function of time and thus the dependency of the specific product formation rate from the specific biomass growth rate. The results appear in form of trained artificial neural networks from which concrete values can easily be computed. The second purpose is using these results for online estimation of current values for the most important state variables of the fermentation process. One only needs online data of the total carbon dioxide production rate (tCPR) produced and an initial value x of the biomass, i.e., the size of the inoculum, for model evaluation. Hence, given the inoculum size and online values of tCPR, the model can directly be employed as a softsensor for the actual value of the biomass, the product mass as well as the specific biomass growth rate and the specific product formation rate. In this paper the method is applied to fermentation experiments on the laboratory scale with an E. coli strain producing a recombinant protein that appears in form of inclusion bodies within the cells' cytoplasm.

摘要

提出了一种数据驱动模型,该模型可服务于两个重要目的。首先,确定比生长速率和比产物形成速率作为时间的函数,从而确定比产物形成速率对比生物量生长速率的依赖性。结果以经过训练的人工神经网络的形式呈现,从中可以轻松计算出具体值。第二个目的是将这些结果用于在线估计发酵过程中最重要状态变量的当前值。对于模型评估,只需要已产生的总二氧化碳产生速率(tCPR)的在线数据和生物量的初始值x,即接种量的大小。因此,给定接种量大小和tCPR的在线值,该模型可以直接用作生物量实际值、产物质量以及比生物量生长速率和比产物形成速率的软传感器。本文将该方法应用于实验室规模的发酵实验,使用的大肠杆菌菌株产生一种重组蛋白,该蛋白以包涵体的形式出现在细胞质中。

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