Abstract
The topology of the transcription factor network (TFN) of Escherichia coli is far from uniform, with 22 global regulator (GR) proteins controlling one-third of all genes. So far, their production rates cannot be tracked by comparable fluorescent proteins. We developed a library of fluorescent reporters for 16 GRs for this purpose. Each consists of a single-copy plasmid coding for green fluorescent protein (GFP) fused to the full-length copy of the native promoter. We tracked their activity in exponential and stationary growth, as well as under weak and strong stresses. We show that the reporters have high sensitivity and specificity to all stresses tested and detect single-cell variability in transcription rates. Given the influence of GRs on the TFN, we expect that the new library will contribute to dissecting global transcriptional stress-response programs of E. coli. Moreover, the library can be invaluable in bioindustrial applications that tune those programs to, instead of cell growth, favor productivity while reducing energy consumption.
Original language | English |
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Journal | mSystems |
Volume | 9 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2024 |
Publication type | A1 Journal article-refereed |
Keywords
- fluorescent proteins
- global regulators of gene expression
- native promoters
- strain library
- synthetic single-copy plasmids
- transcriptional reporters
Publication forum classification
- Publication forum level 1
ASJC Scopus subject areas
- Microbiology
- Physiology
- Biochemistry
- Ecology, Evolution, Behavior and Systematics
- Modelling and Simulation
- Molecular Biology
- Genetics
- Computer Science Applications