Abstract <p>Lignin, the most abundant renewable source of aromatic compounds on earth, remains underexploited in traditional biorefining. Fraxetin, a naturally occurring flavonoid, has garnered considerable attention in the scientific community due to its diverse and potent biological activities such as antimicrobial, anticancer, antioxidant, anti-inflammatory, and neurological protective actions. To enhance the green and value-added utilization of lignin, <i>Saccharomyces cerevisiae</i> was engineered as a cell factory to transform lignin derivatives to produce fraxetin. The expression of scopoletin 8-hydroxylase (S8H) and coumarin synthase (COSY) enabled <i>S. cerevisiae</i> to produce fraxetin from ferulic acid, one of the three principal monomers. The optimized fermentation strategies produced 19.1&#xa0;mg/L fraxetin from ferulic acid by engineered <i>S. cerevisiae</i>. Additionally, the engineered cell factory achieved a fraxetin titer of 7.7&#xa0;mg/L in lignin hydrolysate. This study successfully demonstrates the biotransformation of lignin monomers and lignin hydrolysate into fraxetin using a <i>S. cerevisiae</i> cell factory, thereby providing a viable strategy for the valorization of lignin.</p> Key points <p><i>• AtS8H showed substance specificity in the hydroxylation of scopoletin.</i></p> <p><i>• AtCOSY and AtS8H were key enzymes for converting ferulic acid into fraxetin.</i></p> <p><i>• Yeast was engineered to produce fraxetin from lignin hydrolysate.</i></p>

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Engineering yeast to produce fraxetin from ferulic acid and lignin

  • Bo-Tao He,
  • Bing-Zhi Li

摘要

Abstract

Lignin, the most abundant renewable source of aromatic compounds on earth, remains underexploited in traditional biorefining. Fraxetin, a naturally occurring flavonoid, has garnered considerable attention in the scientific community due to its diverse and potent biological activities such as antimicrobial, anticancer, antioxidant, anti-inflammatory, and neurological protective actions. To enhance the green and value-added utilization of lignin, Saccharomyces cerevisiae was engineered as a cell factory to transform lignin derivatives to produce fraxetin. The expression of scopoletin 8-hydroxylase (S8H) and coumarin synthase (COSY) enabled S. cerevisiae to produce fraxetin from ferulic acid, one of the three principal monomers. The optimized fermentation strategies produced 19.1 mg/L fraxetin from ferulic acid by engineered S. cerevisiae. Additionally, the engineered cell factory achieved a fraxetin titer of 7.7 mg/L in lignin hydrolysate. This study successfully demonstrates the biotransformation of lignin monomers and lignin hydrolysate into fraxetin using a S. cerevisiae cell factory, thereby providing a viable strategy for the valorization of lignin.

Key points

• AtS8H showed substance specificity in the hydroxylation of scopoletin.

• AtCOSY and AtS8H were key enzymes for converting ferulic acid into fraxetin.

• Yeast was engineered to produce fraxetin from lignin hydrolysate.