# De novo biosynthesis of eriocitrin in Saccharomyces cerevisiae through deep learning-guided enzyme screening and systematic metabolic engineering

**Authors:** Qiyuan Lu, Xinjia Tan, Siqi Zhang, Yongtong Wang, Yifei Zhao, Juan Liu, Fanglin Hu, Shasha Zuo, Jiaxu Chen, Liusha Fan, Shenghua Ding, Zhiqiang Xiao, Yang Shan

PMC · DOI: 10.1016/j.synbio.2026.01.019 · Synthetic and Systems Biotechnology · 2026-02-04

## TL;DR

Scientists engineered yeast to produce eriocitrin, a beneficial compound, using deep learning and metabolic engineering, offering a sustainable alternative to plant extraction.

## Contribution

A de novo biosynthetic pathway for eriocitrin in yeast using deep learning-guided enzyme screening and metabolic engineering.

## Key findings

- Eriocitrin titer of 147.9 mg/L achieved with eriodictyol supplementation.
- Eriodictyol titer of 237.8 mg/L obtained through optimized strain engineering.
- De novo eriocitrin production reached 30.5 mg/L in a fully engineered yeast strain.

## Abstract

Eriocitrin, a flavanone-7-O-disaccharide known for its antioxidant and anti-inflammatory properties, holds considerable promise for use in functional foods and pharmaceuticals. However, its large-scale production is constrained by the limitations of conventional plant extraction, including low abundance of active compounds and seasonal variability. Here, we established a de novo biosynthetic pathway for eriocitrin from glucose in engineered Saccharomyces cerevisiae through combinatorial metabolic engineering. First, to verify the feasibility of glycosylation in the eriocitrin synthesis process, two highly efficient flavonoid-7-O-glucosyltransferases were identified using an integrated bioinformatics and deep learning approach. Subsequently, through the reconstruction of the UDP-rhamnose synthesis pathway and enhancement of the key glycosylation precursor UDP-glucose supply, an eriocitrin titer of 147.9 mg/L was achieved following supplementation with 300 mg/L eriodictyol. To further achieve the de novo synthesis of eriocitrin, an eriodictyol-producing strain was developed by screening the optimal F3′H/CPR pair, engineering promoters, and pathway integration, achieving an eriodictyol titer of 237.8 mg/L. Finally, combining the eriodictyol-producing chassis strain with the previously optimized glycosylation module enabled the de novo production of eriocitrin, reaching a titer of 30.5 mg/L. This work demonstrates a proof-of-concept for microbial production of flavonoid disaccharides, providing a foundation for a sustainable and scalable supply of eriocitrin.

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## Linked entities

- **Proteins:** F3H (flavanone 3-hydroxylase), POR (cytochrome p450 oxidoreductase)
- **Chemicals:** eriocitrin (PubChem CID 83489), glucose (PubChem CID 5793), UDP-rhamnose (PubChem CID 192751), UDP-glucose (PubChem CID 8629), eriodictyol (PubChem CID 11095)
- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** eriodictyol (MESH:C007619), glucose (MESH:D005947), UDP-rhamnose (MESH:C022183), Eriocitrin (MESH:C114706), UDP-glucose (MESH:D014532), flavanone-7-O-disaccharide (-)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12905779/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12905779/full.md

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Source: https://tomesphere.com/paper/PMC12905779