4.5 Article

Conformation control of the histidine kinase BceS ofBacillus subtilisby its cognate ABC-transporter facilitates need-based activation of antibiotic resistance

期刊

MOLECULAR MICROBIOLOGY
卷 115, 期 1, 页码 157-174

出版社

WILEY
DOI: 10.1111/mmi.14607

关键词

antimicrobial peptide; cell envelope stress; flux-sensing; signal transduction

资金

  1. Biotechnology and Biological Sciences Research Council [BB/M026280/1, BB/M029255/1]
  2. BBSRC [BB/M026280/1, BB/M029255/1] Funding Source: UKRI

向作者/读者索取更多资源

Bacteria tightly control gene expression to minimize fitness costs associated with antibiotic resistance. In Bacillus subtilis, a novel regulatory logic involving a two-component system and an ABC transporter allows direct monitoring of detoxification needs. The transporter not only activates the kinase, but also helps maintain its inactive state, ensuring precise flux-dependent signaling control. Transport flux-dependent signaling conserves energy and provides a unique strategy for energy-efficient decision making.
Bacteria closely control gene expression to ensure optimal physiological responses to their environment. Such careful gene expression can minimize the fitness cost associated with antibiotic resistance. We previously described a novel regulatory logic inBacillus subtilisenabling the cell to directly monitor its need for detoxification. This cost-effective strategy is achieved via a two-component regulatory system (BceRS) working in a sensory complex with an ABC-transporter (BceAB), together acting as a flux-sensor where signaling is proportional to transport activity. How this is realized at the molecular level has remained unknown. Using experimentation and computation we here show that the histidine kinase is activated by piston-like displacements in the membrane, which are converted to helical rotations in the catalytic core via an intervening HAMP-like domain. Intriguingly, the transporter was not only required for kinase activation, but also to actively maintain the kinase in its inactive state in the absence of antibiotics. Such coupling of kinase activity to that of the transporter ensures the complete control required for transport flux-dependent signaling. Moreover, we show that the transporter likely conserves energy by signaling with sub-maximal sensitivity. These results provide the first mechanistic insights into transport flux-dependent signaling, a unique strategy for energy-efficient decision making.

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