Abstract
Phosphatidylglycerol (PG) is a valuable product across pharmaceuticals, cosmetics and food industries, the conventional phospholipase D (PLD) syntheses however require organic solvents and very long reaction times to reach 50-74% yield at millilitre scale. The novelty of this study is that we have developed a solvent-free, fully aqueous synthesis route of PG using PLD-catalysed transphosphatidylation of phosphatidylcholine (PC) with glycerol in a 250 mL oscillatory baffled reactor (OBR). By optimising temperature, PLD concentration, glycerol-to-PC ratio and mixing, we achieved 63.5% PG conversion within 20 minutes with no detectable byproduct. Time-resolved kinetic analysis has revealed a three-phase mechanism in this reaction: an initial Michaelis–Menten behaviour, followed by product inhibition and eventual enzyme deactivation. We have then developed a multi-parameter kinetic model integrating intrinsic enzyme kinetics with operational variables, enabling quantitative predictions of reaction concentration, conversion and selectivity at high confidence level (R2>0.95). Coupling the green, solvent-free process with reactor intensification and mechanistic modelling establishes a scalable framework for PG manufacture and offers regulatory and sustainability advantages by avoiding volatile organic solvents and simplifying downstream processing.
| Original language | English |
|---|---|
| Article number | 101004 |
| Journal | Chemical Engineering Journal Advances |
| Volume | 25 |
| Early online date | 22 Dec 2025 |
| DOIs | |
| Publication status | Published - Mar 2026 |
Keywords
- Green chemistry
- Kinetic modeling
- Oscillatory baffled reactor
- Phosphatidylglycerol
- Transphosphatidylation
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry
- General Chemical Engineering
- Industrial and Manufacturing Engineering
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