AI-Guided Design and Predictive Modeling of Synthetic Escherichia coli Promoters through Comprehensive −10/–35 Box Engineering
Abstract
Promoters are essential in transcriptional regulation, with the −10 and −35 boxes playing a critical role in determining their strength. Modulating these regions can effectively fine-tune promoter strength. However, the lack of a clear quantitative relationship between sequence composition and transcriptional output impedes the rational design of promoters. To address this, we developed a synthetic promoter library by varying RNA polymerase binding energies at the −10 and −35 boxes. The library was partitioned into four sublibraries with expression strengths spanning an 80-fold range. Using fluorescence-activated cell sorting followed by sequencing, we identified 20,799 distinct promoters. Analysis of this library uncovered distinct sequence-activity patterns, including a small subset of −35 box sequences that consistently conferred high transcriptional output across diverse −10 partners. Based on this, we developed an artificial intelligence platform that integrates a convolutional neural network for strength prediction (Pearson’s r = 0.84) with a balanced generative adversarial network incorporating a gradient penalty for de novo promoter design. By coupling these models, we achieved a precise design of promoters with user-defined strengths ( r = 0.85), establishing a bidirectional framework that links −10/–35 boxes to transcriptional activity through deep learning. This study expands the sequence diversity of functional −10 and −35 boxes in E. coli, provides a predictive platform for rational promoter engineering, and deciphers combinatorial motif interactions governing transcriptional regulation.
Fields of Study & Subjects
Bacterial Genetics and Biotechnology
Gene Regulatory Network Analysis
Genomics and Chromatin Dynamics
Publication details
- Journal / source
- ACS Synthetic Biology
- Publisher
- American Chemical Society (ACS)
- Volume
- 15
- Issue
- 2
- Pages
- 728–739
- Publication date
- 27 January 2026
- Language
- EN