# Single cell profiling framework reveals metabolic subpopulations as drivers of bioproduction heterogeneity

**Authors:** Juline Savigny, Kiyan Shabestary, Maria Portela, Cinzia Klemm, Yvette Sum, Piotr Hapeta, Marko Storch, Christopher Rowlands, Rodrigo Ledesma-Amaro

PMC · DOI: 10.1038/s41467-025-67408-x · Nature Communications · 2025-12-21

## TL;DR

A new framework using single-cell biosensors identifies metabolic subpopulations that affect bioproduction yields and offers strategies to improve them.

## Contribution

A biosensor-based toolkit for analyzing and modulating single-cell metabolic heterogeneity in microbial cell factories.

## Key findings

- Glucose depletion induces metabolically distinct subpopulations with differing production capabilities.
- Lower intracellular pH subpopulations enhance violacein production but reduce lycopene yields.
- Galactose cultivation shifts subpopulation dynamics to favor higher lycopene-producing phenotypes.

## Abstract

Heterogeneity within clonal cell populations remains a critical bottleneck within bioprocess engineering, notably by undermining bioproduction yields. Efforts to mitigate its impact have, however, been hampered by technological difficulties quantifying metabolism at the single-cell level. Here, we propose a framework based on single-cell biosensor analysis that enables robust characterisation of cell’s metabolic states, leveraging it to detect and isolate isogeneic heterogeneity in response to environmental perturbations and within microbial cell factories. We identify acute and gradual glucose depletion to induce differentiation of metabolically distinct subpopulations and reveal these subpopulations to exhibit differential production capabilities, with lower intracellular pH subpopulations exhibiting enhanced product accumulation within violacein-producing strains but reduced yields within lycopene-producing strains. Lastly, we highlight galactose cultivation as a method to modulate subpopulation dynamics towards higher-producing lycopene phenotypes. Altogether, our research provides insights into subpopulation differentiation and establishes promising avenues for the engineering of more robust and higher-producing strains.

Heterogeneity within clonal cell populations affects bioprocess engineering. Here, the authors report a biosensor-based toolkit to investigate phenotypic heterogeneity in engineered yeast, reveal pH-based subpopulations and metabolite production states, and modulate/shift subpopulation dynamics to increase lycopene production.

## Linked entities

- **Chemicals:** glucose (PubChem CID 5793), violacein (PubChem CID 11053), lycopene (PubChem CID 446925), galactose (PubChem CID 6036)

## Full-text entities

- **Chemicals:** glucose (MESH:D005947), galactose (MESH:D005690), lycopene (MESH:D000077276), violacein (MESH:C063155)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12816005/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12816005/full.md

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Source: https://tomesphere.com/paper/PMC12816005