In this section
@article{Chen:2026:10.1038/s41589-025-02081-1,
author = {Chen, H and Peng, H and Ellis, T and Ledesma-Amaro, R},
doi = {10.1038/s41589-025-02081-1},
journal = {Nature Chemical Biology},
title = {Programmable cell–cell adhesion in synthetic yeast communities for improved bioproduction},
url = {http://dx.doi.org/10.1038/s41589-025-02081-1},
year = {2026}
}
TY - JOUR
AB - 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.
AU - Chen,H
AU - Peng,H
AU - Ellis,T
AU - Ledesma-Amaro,R
DO - 10.1038/s41589-025-02081-1
PY - 2026///
SN - 1552-4450
TI - Programmable cell–cell adhesion in synthetic yeast communities for improved bioproduction
T2 - Nature Chemical Biology
UR - http://dx.doi.org/10.1038/s41589-025-02081-1
UR - https://doi.org/10.1038/s41589-025-02081-1
ER -
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