Reciprocal growth control by competitive binding of nucleotide second messengers to a metabolic switch in Caulobacter crescentus.
Viktoriya ShypBadri Nath DubeyRaphael BöhmJohannes HartlJutta NesperJulia A VorholtSebastian HillerTilman SchirmerUrs JenalPublished in: Nature microbiology (2020)
Bacteria use small signalling molecules such as (p)ppGpp or c-di-GMP to tune their physiology in response to environmental changes. It remains unclear whether these regulatory networks operate independently or whether they interact to optimize bacterial growth and survival. We report that (p)ppGpp and c-di-GMP reciprocally regulate the growth of Caulobacter crescentus by converging on a single small-molecule-binding protein, SmbA. While c-di-GMP binding inhibits SmbA, (p)ppGpp competes for the same binding site to sustain SmbA activity. We demonstrate that (p)ppGpp specifically promotes Caulobacter growth on glucose, whereas c-di-GMP inhibits glucose consumption. We find that SmbA contributes to this metabolic switch and promotes growth on glucose by quenching the associated redox stress. The identification of an effector protein that acts as a central regulatory hub for two global second messengers opens up future studies on specific crosstalk between small-molecule-based regulatory networks.
Keyphrases
- small molecule
- biofilm formation
- binding protein
- transcription factor
- pseudomonas aeruginosa
- protein protein
- type diabetes
- blood glucose
- staphylococcus aureus
- escherichia coli
- metabolic syndrome
- candida albicans
- adipose tissue
- climate change
- amino acid
- cystic fibrosis
- blood pressure
- current status
- regulatory t cells
- human health