Keywords

transcriptional biosensors, metabolic engineering, synthetic biology, whole-cell biocatalysts

Abstract

Cell factories converting bio-based precursors to chemicals present an attractive avenue to a sustainable economy, yet screening of genetically diverse strain libraries to identify the best-performing whole-cell biocatalysts is a low-throughput endeavor. For this reason, transcriptional biosensors attract attention as they allow the screening of vast libraries when used in combination with fluorescence-activated cell sorting (FACS). However, broad ligand specificity of transcriptional regulators (TRs) often prohibits the development of such ultra-high-throughput screens. Here, we solve the structure of the TR LysG of Corynebacterium glutamicum, which detects all three basic amino acids. Based on this information, we follow a semi-rational engineering approach using a FACS-based screening/counterscreening strategy to generate an l-lysine insensitive LysG-based biosensor. This biosensor can be used to isolate l-histidine-producing strains by FACS, showing that TR engineering towards a more focused ligand spectrum can expand the scope of application of such metabolite sensors.

Original Publication Citation

Della Corte, D., van Beek, H.L., Syberg, F. et al. Engineering and application of a biosensor with focused ligand specificity. Nat Commun 11, 4851 (2020). https://doi.org/10.1038/s41467-020-18400-0

Document Type

Peer-Reviewed Article

Publication Date

2020-09-25

Publisher

Nat Commun 11

Language

English

College

Computational, Mathematical and Physical Sciences

Department

Physics and Astronomy

University Standing at Time of Publication

Associate Professor

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