# A growth-coupled progesterone-responsive biosensor for high-throughput microfluidic screening in Saccharomyces cerevisiae

**Authors:** Yucheng Hu, Jinde Chen, Shaofang Tian, Yang Zhang, Zhiqian Zhang, Ao Jiang, Yi-Rui Wu, Baoshun Zhang

PMC · DOI: 10.1016/j.synbio.2025.12.004 · 2026-01-02

## TL;DR

A new biosensor in yeast helps screen for better steroid production, overcoming solubility issues and enabling high-throughput strain selection.

## Contribution

A growth-coupled, progesterone-responsive biosensor system in yeast for high-throughput screening of steroid-producing strains.

## Key findings

- Five yeast variants showed 2.0–3.37-fold higher progesterone production than wild-type.
- Microfluidic droplet encapsulation effectively separated high-producers.
- The system is modular and adaptable for other bioactive molecules.

## Abstract

Poor aqueous solubility of steroid precursors, such as pregnenolone and progesterone, limits microbial biotransformation and high-throughput strain screening, representing a bottleneck for strain improvement and potential industrial applications.

To address this, we developed a growth-coupled progesterone-responsive biosensor in Saccharomyces cerevisiae, integrated with a hydroxypropyl-β-cyclodextrin (HP-β-CD) system to enhance intracellular steroid availability. The biosensor links progesterone formation to cell growth and fluorescence, with selection stringency finely tuned via an IPTG-inducible lac operator and 3-aminotriazole (3-AT) to suppress low-producing cells. Coupled with atmospheric and room temperature plasma (ARTP) mutagenesis, the growth-coupled biosensor–FADS platform identified five yeast variants capable of improved conversion of pregnenolone to progesterone while expressing 3β-hydroxysteroid dehydrogenase (3β-HSD) without altering the enzyme itself. The progesterone production of these selected variants was subsequently validated using 1 mM pregnenolone as the substrate, showing 2.0–3.37-fold higher titers than the wild-type strain, demonstrating proof-of-concept. Microfluidic droplet encapsulation allowed clear separation of high-producers, highlighting the platform's selectivity, robustness, and scalability. This synthetic biology–driven system integration platform provides a practical, modular, and high-throughput strategy for screening poorly water-soluble steroid-producing yeast. It is adaptable to other bioactive molecules, can support future enzyme evolution, and demonstrates potential for broader biotechnological applications.

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## Linked entities

- **Proteins:** 3BHSD (3beta-hydroxysteroid dehydrogenase/isomerase)
- **Chemicals:** pregnenolone (PubChem CID 8955), progesterone (PubChem CID 5994), HP-β-CD (PubChem CID 138059664), IPTG (PubChem CID 656894), 3-aminotriazole (PubChem CID 1639), 3-AT (PubChem CID 1639)
- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Chemicals:** progesterone (MESH:D011374), water (MESH:D014867), hydroxypropyl-beta-cyclodextrin (MESH:D000073738), steroid (MESH:D013256), beta-CD (MESH:C031215), 3-AT (-), pregnenolone (MESH:D011284), IPTG (MESH:D007544)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12805089/full.md

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Source: https://tomesphere.com/paper/PMC12805089