Abstract
Bioprocesses are inherently multiscale, spanning intracellular metabolism to production-scale reactors. Simulation models that integrate these scales offer potential strategies to study the effect of changing metabolic states and enable efficient integration of biological knowledge gathered from lab-scale experiments. In this study, we demonstrate the potential of such simulation model towards the production of mevalonate, an important pharmaceutical drug compound produced through fermentation of a fungal species Aspergillus terreus. We integrate a genome-scale metabolic model of the organism with a plant-wide simulation model for the bioprocess that encompasses several upstream and downstream unit operations. Through this integration, we identify potential targets for metabolic engineering towards increased product flux and simultaneously estimate the associated oxygen requirements. This framework serves as a foundation for developing digital twins of bioprocesses that bridges strain engineering with process design and operations.
| Original language | English |
|---|---|
| Book series | Systems & Control Transactions |
| Volume | 5 |
| Pages (from-to) | 709-713 |
| ISSN | 2818-4734 |
| DOIs | |
| Publication status | Published - 2026 |
| Event | 36th European Symposium on Computer Aided Process Engineering : ESCAPE 36 - University of Sheffield, Sheffield, United Kingdom Duration: 21 Jun 2026 → 24 Jun 2026 |
Conference
| Conference | 36th European Symposium on Computer Aided Process Engineering |
|---|---|
| Location | University of Sheffield |
| Country/Territory | United Kingdom |
| City | Sheffield |
| Period | 21/06/2026 → 24/06/2026 |
Keywords
- Simulation
- Biosystems
- Fermentation
- Optimization
- Multiscale Modelling
- Metabolic models
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