Programmable cell–cell adhesion in synthetic yeast communities for improved bioproduction
In multicellular systems, engineering-controlled cell-cell adhesion and metabolic interdependence are vital for developing complex functionalities. This study introduces a yeast synthetic toolbox for modular cell-cell adhesion and cocultures, aiming to overcome the limitations of existing approaches that lack genetic specificity and control. First, a model yeast strain 007Δ is created with seven main flocculation and agglutination genes removed, providing a clean background for synthetic adhesion systems. Then, three distinct adhesion pair systems-Strategy 1, Strategy 2.1 and Strategy 2.2-are established involving yeast flocculation and agglutination proteins and yeast surface display systems. In addition, a quantitative assessment is conducted on the adhesive specificity and strength, alongside the capability of synthetic adhesion to generate patterns. Finally, we successfully demonstrate enhanced bioproduction of the high-value food antioxidant, resveratrol, utilizing synthetic cocultures coupled with cell adhesion systems. We anticipate that this toolkit will emerge as a valuable resource for diverse applications in synthetic biology and biomanufacturing.
Authors
- Huadong Peng (ORCID: https://orcid.org/0009-0000-6544-273X)
- Tom Ellis (ORCID: https://orcid.org/0000-0001-5392-976X)
- Rodrigo Ledesma-Amaro
- Haohong Chen
Institutions
- The University of Queensland (AU)
- ARC Centre of Excellence in Synthetic Biology (AU)
- Imperial College London (GB)
- South China University of Technology (CN)
Publication Details
- Journal
- Nature Chemical Biology
- Published
- 2026-01-05
- DOI
- https://doi.org/10.1038/s41589-025-02081-1
- Citations
- 1
- Primary Topic
- Biochemical and Structural Characterization
- Type
- article
- Field-Weighted Citation Impact
- 22.24