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Article

Modelling of Escherichia coli Batch and Fed-Batch Processes in Semi-Defined Yeast Extract Media

by
Fabian Schröder-Kleeberg
1,
Markus Zoellkau
2,
Markus Glaser
2,
Christian Bosch
3,
Markus Brunner
3,
Mariano Nicolas Cruz Bournazou
1 and
Peter Neubauer
1,*
1
Department of Bioprocess Engineering, Institute of Biotechnology, Technische Universität Berlin, Ackerstr. 76, 13355 Berlin, Germany
2
Wacker Biotech GmbH, 07745 Jena, Germany
3
Wacker Chemie AG, 81379 München, Germany
*
Author to whom correspondence should be addressed.
Bioengineering 2025, 12(10), 1081; https://doi.org/10.3390/bioengineering12101081 (registering DOI)
Submission received: 22 August 2025 / Revised: 17 September 2025 / Accepted: 18 September 2025 / Published: 4 October 2025
(This article belongs to the Section Biochemical Engineering)

Abstract

Model-based approaches provide increasingly advanced opportunities for optimizing and accelerating bioprocess development. However, to accurately capture the complexity of biotechnological processes, continuous refinement of suitable models remains essential. A crucial gap in this field has been the lack of suitable model for describing Escherichia coli growth in cultivation media containing yeast extract, while accounting for key bioprocess parameters such as biomass, substrate, acetate, and oxygen. To address this, a published mechanistic macro-kinetic model for E. coli was extended with a set of mathematical equations that describe key aspects of the uptake of yeast extract. The underlying macro-kinetic approach is based on the utilization of amino acids in E. coli, where growth is primarily influenced by two distinct classes of amino acids. Using fed-batch cultivation data from an E. coli K-12 strain supplemented with yeast extract, it was demonstrated that the proposed model extensions were essential for accurately representing the bioprocess. This approach was further validated through fitting the model on cultivation data from five different yeast extracts sourced from various manufacturers. Additionally, the model enabled reliable predictions of growth dynamics across a range of yeast extract concentrations up to 20 g L−1. Further differentiation of the data into batch and fed-batch revealed that for less complex datasets, such as those obtained from a batch phase, a simplified model can be sufficient. Due to its modular structure, the developed model provides the necessary flexibility to serve as a tool for the development, optimization, and control of E. coli cultivations with and without yeast extract.
Keywords: model-based bioprocess development; Escherichia coli; fed-batch, yeast extract; mechanistic model; macro-kinetic model; semi-defined media; complex additives model-based bioprocess development; Escherichia coli; fed-batch, yeast extract; mechanistic model; macro-kinetic model; semi-defined media; complex additives

Share and Cite

MDPI and ACS Style

Schröder-Kleeberg, F.; Zoellkau, M.; Glaser, M.; Bosch, C.; Brunner, M.; Cruz Bournazou, M.N.; Neubauer, P. Modelling of Escherichia coli Batch and Fed-Batch Processes in Semi-Defined Yeast Extract Media. Bioengineering 2025, 12, 1081. https://doi.org/10.3390/bioengineering12101081

AMA Style

Schröder-Kleeberg F, Zoellkau M, Glaser M, Bosch C, Brunner M, Cruz Bournazou MN, Neubauer P. Modelling of Escherichia coli Batch and Fed-Batch Processes in Semi-Defined Yeast Extract Media. Bioengineering. 2025; 12(10):1081. https://doi.org/10.3390/bioengineering12101081

Chicago/Turabian Style

Schröder-Kleeberg, Fabian, Markus Zoellkau, Markus Glaser, Christian Bosch, Markus Brunner, Mariano Nicolas Cruz Bournazou, and Peter Neubauer. 2025. "Modelling of Escherichia coli Batch and Fed-Batch Processes in Semi-Defined Yeast Extract Media" Bioengineering 12, no. 10: 1081. https://doi.org/10.3390/bioengineering12101081

APA Style

Schröder-Kleeberg, F., Zoellkau, M., Glaser, M., Bosch, C., Brunner, M., Cruz Bournazou, M. N., & Neubauer, P. (2025). Modelling of Escherichia coli Batch and Fed-Batch Processes in Semi-Defined Yeast Extract Media. Bioengineering, 12(10), 1081. https://doi.org/10.3390/bioengineering12101081

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