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Article Abstract
Curcumin is a natural phenylpropanoid compound with various biological activities and is widely used in food and pharmaceuticals. A curcumin biosynthetic pathway was constructed in BL21(DE3). Optimization of the curcumin biosynthesis module achieved a curcumin titer of 26.8 ± 0.6 mg/L. Regulating the metabolic fluxes of the β-oxidation pathway and fatty acid elongation cycle and blocking the endogenous malonyl-CoA consumption pathway increased the titer to 113.6 ± 7.1 mg/L. Knockout of endogenous curcumin reductase () and intermediate product detoxification by heterologous expression of the solvent-resistant pump () increased the titer to 137.5 ± 3.0 mg/L. A 5 L pilot-scale fermentation, using a three-stage pH alternation strategy, increased the titer to 696.2 ± 20.9 mg/L, 178.5-fold higher than the highest curcumin titer from biosynthesis previously reported, thereby laying the foundation for efficient biosynthesis of curcumin and its derivatives.
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