Abstract
In metabolic engineering, increasing chemical production usually involves manipulating the expression levels of key enzymes. However, limited synthetic tools exist for modulating enzyme activity beyond the transcription level. Inspired by natural post-translational mechanisms, we present targeted enzyme degradation mediated by optically controlled nanobodies. We applied this method to a branched biosynthetic pathway, deoxyviolacein, and observed enhanced product specificity and yield. We then extend the biosynthesis pathway to violacein and show how simultaneous degradation of two target enzymes can further shift production profiles. Through the redirection of metabolic flux, we demonstrate how targeted enzyme degradation can be used to minimize unwanted intermediates and boost the formation of desired products.
Original language | English (US) |
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Pages (from-to) | 4110-4118 |
Number of pages | 9 |
Journal | ACS Synthetic Biology |
Volume | 13 |
Issue number | 12 |
DOIs | |
State | Published - Dec 20 2024 |
All Science Journal Classification (ASJC) codes
- Biomedical Engineering
- Biochemistry, Genetics and Molecular Biology (miscellaneous)
Keywords
- dynamic control
- metabolic engineering
- nanobody
- optogenetics
- Saccharomyces cerevisiae
- targeted protein degradation