9DT3 image
Deposition Date 2024-09-30
Release Date 2025-10-08
Last Version Date 2026-06-24
Entry Detail
PDB ID:
9DT3
Title:
Crystal structure of the engineered sulfonylurea repressor EsR (L11-C6), bound to ethametsulfuron-methyl
Biological Source:
Source Organism(s):
Escherichia coli (Taxon ID: 562)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
2.80 Å
R-Value Free:
0.27
R-Value Work:
0.19
Space Group:
P 1 21 1
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Sulfonylurea repressor EsR (L
Gene (Uniprot):tetR
Chain IDs:A, B, C, D
Chain Length:207
Number of Molecules:4
Biological Source:Escherichia coli
Ligand Molecules
Primary Citation
Design and evolution of the tetracycline repressor into sulfonylurea herbicide-responsive gene switches for field crops.
Nat Commun ? ? ? (2026)
PMID: 42259793 DOI: 10.1038/s41467-026-73848-w

Abstact

Chemically inducible expression systems enable transgene expression regulation in response to external small molecules. Tetracycline repressor (TetR)-based gene switches work in plants, but antibiotics are neither approved nor advisable for crop use. Here we report engineering of TetR mutants that respond to approved sulfonylurea (SU) herbicides instead of antibiotics. Designed variants show low-nanomolar EC(50) values for ethametsulfuron-methyl (Es) or chlorsulfuron and tightly bind the Tet operator sequence, but only in the absence of corresponding SUs. Crystal structures of two repressors in complex with their respective SU ligands reveal extensive interactions explaining their strong binding. The Es repressor-based gene switch is introduced into tobacco, soybean, maize, rice, and Arabidopsis, and robust reporter gene activation is observed upon herbicide application. Addition of a repressor-regulated siRNA targeting the repressor transcript increases the magnitude and spatial distribution of the response following herbicide treatment and results in a partially bistable gene switch. The SU repressors also function well in mammalian cell culture and may enable regulation of additional genes in conjunction with TetR.

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Primary Citation of related structures
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