Model-based optimisation of a batch reactor with a coupled bi-enzymatic process for mannitol production. (2nd February 2020)
- Record Type:
- Journal Article
- Title:
- Model-based optimisation of a batch reactor with a coupled bi-enzymatic process for mannitol production. (2nd February 2020)
- Main Title:
- Model-based optimisation of a batch reactor with a coupled bi-enzymatic process for mannitol production
- Authors:
- Maria, Gheorghe
- Abstract:
- Highlights: Fructose (F) is reduced to mannitol (M) using MDH (mannitol dehydrogenase) and NADH. Cofactor NADH is in-situ continuously recovered by the expense of formate degradation. Formate enzymatic degradation takes place simultaneously in the presence of free FDH. Model-based simulation allows optimization of coupled reactions in a batch reactor. For an imposed fructose reduction conversion, enzyme consumption is minimized. Abstract: Multi-enzymatic reactions are effective alternatives to complex chemical syntheses, using milder reaction conditions, and generating less waste. One essential engineering problem concerns derivation of an optimal operation policy of the chosen reactor. For coupled enzymatic systems, model-based calculations turn into difficult optimization problem to be solved for every particular system. The paper exemplifies model-based identification of the optimal operating policy of a bi-enzymatic batch reactor (BR), that minimizes enzyme consumption for an imposed productivity. Exemplification refers to the enzymatic reduction of d -fructose to mannitol by using suspended MDH and NADH cofactor, with in-situ continuous regeneration of NADH by the expense of formate enzymatic degradation. As novelty items are worth mentioning: (i) highlighting the close connection between the coupling reactions, enzyme concentrations, and quasi-stationary NADH/NAD ratio over the batch; (ii) how a lumped but adequately dynamic model can successfully support in silicoHighlights: Fructose (F) is reduced to mannitol (M) using MDH (mannitol dehydrogenase) and NADH. Cofactor NADH is in-situ continuously recovered by the expense of formate degradation. Formate enzymatic degradation takes place simultaneously in the presence of free FDH. Model-based simulation allows optimization of coupled reactions in a batch reactor. For an imposed fructose reduction conversion, enzyme consumption is minimized. Abstract: Multi-enzymatic reactions are effective alternatives to complex chemical syntheses, using milder reaction conditions, and generating less waste. One essential engineering problem concerns derivation of an optimal operation policy of the chosen reactor. For coupled enzymatic systems, model-based calculations turn into difficult optimization problem to be solved for every particular system. The paper exemplifies model-based identification of the optimal operating policy of a bi-enzymatic batch reactor (BR), that minimizes enzyme consumption for an imposed productivity. Exemplification refers to the enzymatic reduction of d -fructose to mannitol by using suspended MDH and NADH cofactor, with in-situ continuous regeneration of NADH by the expense of formate enzymatic degradation. As novelty items are worth mentioning: (i) highlighting the close connection between the coupling reactions, enzyme concentrations, and quasi-stationary NADH/NAD ratio over the batch; (ii) how a lumped but adequately dynamic model can successfully support in silico engineering evaluations by aiming to optimize the BR operation. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Computers & chemical engineering. Volume 133(2020)
- Journal:
- Computers & chemical engineering
- Issue:
- Volume 133(2020)
- Issue Display:
- Volume 133, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 133
- Issue:
- 2020
- Issue Sort Value:
- 2020-0133-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-02-02
- Subjects:
- D-fructose reduction -- D-Mannitol production -- Batch reactor optimization -- Mannitol dehydrogenase -- Formate dehydrogenase -- Coenzyme NADH regeneration
Chemical engineering -- Data processing -- Periodicals
660.0285 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00981354 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.compchemeng.2019.106628 ↗
- Languages:
- English
- ISSNs:
- 0098-1354
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3394.664000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12524.xml