High Sensitivity of the rpiAB Escherichia coli Mutants to Antibiotics Is Associated with the Participation of the deo-Operon in a Hypothetical Ribose-5-Phosphate Futile Cycle
Open Access
Abstract
Previously, we demonstrated that disruption of ribose-5-phosphate biosynthesis in the pentose phosphate pathway increases the sensitivity of E. coli bacteria to a broad spectrum of antibiotics, and this sensitivity can be suppressed by deletion of the deoB gene. In this study, we showed that antibiotic sensitivity can also be suppressed by the deletion of the apt gene, which, along with the deoBD genes, constitutes the salvage pathway for purine base uptake. We propose that in the rpiAB mutant, these genes, together with the prs gene responsible for phosphoribosyl pyrophosphate (PRPP) synthesis, participate in a futile cycle, converting ATP to AMP and pyrophosphate (PPi). The data obtained on the genetic complementation of deletions of the apt and deoBD genes, combined with restored ATP levels in the rpiAB mutant cells, support the model of the hypothetical futile cycle of ribose-5-phosphate.Keywords
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Funding Information
- Russian Science Foundation (24-14-00089)
This publication has 35 references indexed in Scilit:
- Genome‐wide screen reveals a universal role of ATP in ciprofloxacin tolerance among genetically distinct Escherichia coli persistersmLife, 2026
- Environmental purines decrease Pseudomonas aeruginosa biofilm formation by disrupting c-di-GMP metabolismCell Reports, 2024
- Futile cycles: Emerging utility from apparent futilityCell Metabolism, 2024
- Chemical Induction of Aminoglycoside Uptake Overcomes Antibiotic Tolerance and Resistance in Staphylococcus aureusCell Chemical Biology, 2019
- Bacterial Metabolism and Antibiotic EfficacyCell Metabolism, 2019
- A White-Box Machine Learning Approach for Revealing Antibiotic Mechanisms of ActionCell, 2019
- Futile cycling increases sensitivity toward oxidative stress in Escherichia coliMetabolic Engineering, 2015
- Purification and characterization of the deoR repressor of Escherichia coli.The EMBO Journal, 1989
- The structure of tandem regulatory regions in the deo operon of Escherichia coli K12The EMBO Journal, 1982
- On the structure of the deo operon of Escherichia coliMolecular Genetics and Genomics, 1977