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Escherichia coli uses σ factors to quickly control large gene cohorts during stress conditions. While most of its genes respond to a single σ factor, approximately 5% of them have dual σ factor preference. The most common are those responsive to both σ, which controls housekeeping genes, and σ, which activates genes during stationary growth and stresses. Using RNA-seq and flow-cytometry measurements, we show that 'σ genes' are nearly as upregulated in stationary growth as 'σ genes'. Moreover, we find a clear quantitative relationship between their promoter sequence and their response strength to changes in σ levels. We then propose and validate a sequence dependent model of σ genes, with dual sensitivity to σ and σ, that is applicable in the exponential and stationary growth phases, as well in the transient period in between. We further propose a general model, applicable to other stresses and σ factor combinations. Given this, promoters controlling σ genes (and variants) could become important building blocks of synthetic circuits with predictable, sequence-dependent sensitivity to transitions between the exponential and stationary growth phases.
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http://dx.doi.org/10.1016/j.bbagrm.2022.194812 | DOI Listing |
Microbiol Spectr
September 2025
Faculty of Medicine and Medical Sciences, University of Balamand, Tripoli, Lebanon.
In Gram-negative bacteria, resistance-nodulation-division (RND)-type efflux pumps, particularly AcrAB-TolC, play a critical role in mediating resistance to antimicrobial agents and toxic metabolites, contributing to multidrug resistance. is an entomopathogenic bacterium that has garnered significant interest due to its production of bioactive specialized metabolites with anti-inflammatory, antimicrobial, and scavenger deterrent properties. In previous work, we demonstrated that AcrAB confers self-resistance to stilbenes in TT01.
View Article and Find Full Text PDFAnal Chim Acta
November 2025
College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao, 266109, China. Electronic address:
Background: The separation of structural isomers is always a challenging task for liquid chromatography because of their similar physicochemical property. Research has found that materials with regular microporous structures exhibit excellent isomer separation performance. However, as the most easily available chromatographic material, silica stationary phases with regular and small mesopore structure have not yet been prepared, and it remains to be confirmed whether narrow pores in silica materials have the enhancing effect on shape selectivity in the separation of structural isomers.
View Article and Find Full Text PDFPseudomonas aeruginosa is a highly versatile bacterium capable of surviving and often thriving in stressful environmental conditions. Here we report the effect of two environmental conditions, temperature and growth phase, on the P. aeruginosa PAO1 transcriptome.
View Article and Find Full Text PDFmSphere
September 2025
Instituto de Tecnologia Química e Biológica António Xavier, Oeiras, Portugal.
Most strains of produce two toxins, TcdA and TcdB, which are mainly responsible for the disease symptoms. TcdA and TcdB are coded for by genes in the pathogenicity locus (PaLoc). Some epidemic strains, however, such as R20291, of ribotype 027, additionally produce a binary toxin, CDT, coded for by genes in the CDT locus (CdtLoc).
View Article and Find Full Text PDFPLoS Genet
September 2025
Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey, United States of America.
Studies have shown that DNA damage repair systems, including homologous recombination (HR) and the SOS response, are important for fluoroquinolone (FQ) persistence of Escherichia coli, which has been the workhorse organism of persister research. We sought to explore whether those systems are also important for FQ persistence of Pseudomonas aeruginosa, a common cause of lung infections in cystic fibrosis patients, which can be treated with FQs such as ciprofloxacin (CIP). Notably, P.
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