An automated workflow for enhancing microbial bioprocess optimization on a novel microbioreactor platform
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- 作者：Peter Rohe (1)
Deepak Venkanna (1)
Britta Kleine (2)
Roland Freudl (2)
Marco Oldiges (1) - 关键词：Microbioreactor ; Biolector ; Bioprocess development ; Strain screening ; Heterologous protein expression ; Automation ; Liquid ; handling
- 刊名：Microbial Cell Factories
- 出版年：2012
- 出版时间：December 2012
- 年：2012
- 卷：11
- 期：1
- 全文大小：514KB
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Deepak Venkanna (1)
Britta Kleine (2)
Roland Freudl (2)
Marco Oldiges (1)
1. Institute of Bio- and Geosciences, IBG-1: Biotechnology, Systems Biotechnology, Forschungszentrum J眉lich GmbH, 52425, J眉lich, Germany
2. Institute of Bio- and Geosciences, IBG-1: Biotechnology, Systemic Microbiology, Forschungszentrum J眉lich GmbH, 52425, J眉lich, Germany - ISSN：1475-2859
文摘
Background High-throughput methods are widely-used for strain screening effectively resulting in binary information regarding high or low productivity. Nevertheless achieving quantitative and scalable parameters for fast bioprocess development is much more challenging, especially for heterologous protein production. Here, the nature of the foreign protein makes it impossible to predict the, e.g. best expression construct, secretion signal peptide, inductor concentration, induction time, temperature and substrate feed rate in fed-batch operation to name only a few. Therefore, a high number of systematic experiments are necessary to elucidate the best conditions for heterologous expression of each new protein of interest. Results To increase the throughput in bioprocess development, we used a microtiter plate based cultivation system (Biolector) which was fully integrated into a liquid-handling platform enclosed in laminar airflow housing. This automated cultivation platform was used for optimization of the secretory production of a cutinase from Fusarium solani pisi with Corynebacterium glutamicum. The online monitoring of biomass, dissolved oxygen and pH in each of the microtiter plate wells enables to trigger sampling or dosing events with the pipetting robot used for a reliable selection of best performing cutinase producers. In addition to this, further automated methods like media optimization and induction profiling were developed and validated. All biological and bioprocess parameters were exclusively optimized at microtiter plate scale and showed perfect scalable results to 1 L and 20 L stirred tank bioreactor scale. Conclusions The optimization of heterologous protein expression in microbial systems currently requires extensive testing of biological and bioprocess engineering parameters. This can be efficiently boosted by using a microtiter plate cultivation setup embedded into a liquid-handling system, providing more throughput by parallelization and automation. Due to improved statistics by replicate cultivations, automated downstream analysis, and scalable process information, this setup has superior performance compared to standard microtiter plate cultivation.