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Engineering of tnaC -Based Tryptophan Biosensors for Dynamic Control of Violacein Production.
- Source :
-
Journal of agricultural and food chemistry [J Agric Food Chem] 2024 Nov 06; Vol. 72 (44), pp. 24668-24676. Date of Electronic Publication: 2024 Oct 23. - Publication Year :
- 2024
-
Abstract
- Tryptophan not only serves as a fundamental building block for protein synthesis but also acts as a metabolic precursor for a diverse array of high-value chemicals. Although a few tryptophan-responsive biosensors are currently available, there is a growing interest in developing high-performance biosensors. In this study, we create a miniature toolkit of tryptophan biosensors based upon the leader regulatory region of the tnaCAB operon, which is responsible for tryptophan catabolism in Escherichia coli . Four variants are generated by engineering the tnaC leader sequence, which encodes a leader peptide composed of 24 amino acid residues. Subsequently, the performance of both the natural tnaC sequence and its engineered variants is assessed in a reporter strain based on the MazEF toxin-antitoxin system. The results demonstrate that two engineered variants exhibit increased sensitivity to low levels of tryptophan. Moreover, the engineered biosensors are further optimized by replacing the native promoter of tnaC with a phage-derived constitutive promoter. Intriguingly, the engineered biosensors can be reconstructed for extended application in Pseudomonas putida , a robust microbial chassis for metabolic engineering. In summary, our study expands the toolkit of tryptophan biosensors that can be broadly used for the bioproduction of many other high-value tryptophan-derived products.
- Subjects :
- Pseudomonas putida genetics
Pseudomonas putida metabolism
Operon
Tryptophan metabolism
Tryptophan chemistry
Biosensing Techniques methods
Biosensing Techniques instrumentation
Escherichia coli genetics
Escherichia coli metabolism
Metabolic Engineering
Indoles metabolism
Indoles chemistry
Escherichia coli Proteins genetics
Escherichia coli Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5118
- Volume :
- 72
- Issue :
- 44
- Database :
- MEDLINE
- Journal :
- Journal of agricultural and food chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39440815
- Full Text :
- https://doi.org/10.1021/acs.jafc.4c07638