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The Ser/Thr protein kinase PrkC imprints phenotypic memory in Bacillus anthracis spores by phosphorylating the glycolytic enzyme enolase.

Richa VirmaniAndaleeb SajidAnshika SinghalMohita GaurJayadev JoshiAnkur BothraRicha GargRicha MisraVijay Pal SinghVirginie MolleAjay K GoelArchana SinghVipin C KaliaJung-Kul LeeYasha HasijaGunjan AroraYogendra Singh
Published in: The Journal of biological chemistry (2019)
Bacillus anthracis is the causative agent of anthrax in humans, bovine, and other animals. B. anthracis pathogenesis requires differentiation of dormant spores into vegetative cells. The spores inherit cellular components as phenotypic memory from the parent cell, and this memory plays a critical role in facilitating the spores' revival. Because metabolism initiates at the beginning of spore germination, here we metabolically reprogrammed B. anthracis cells to understand the role of glycolytic enzymes in this process. We show that increased expression of enolase (Eno) in the sporulating mother cell decreases germination efficiency. Eno is phosphorylated by the conserved Ser/Thr protein kinase PrkC which decreases the catalytic activity of Eno. We found that phosphorylation also regulates Eno expression and localization, thereby controlling the overall spore germination process. Using MS analysis, we identified the sites of phosphorylation in Eno, and substitution(s) of selected phosphorylation sites helped establish the functional correlation between phosphorylation and Eno activity. We propose that PrkC-mediated regulation of Eno may help sporulating B. anthracis cells in adapting to nutrient deprivation. In summary, to the best of our knowledge, our study provides the first evidence that in sporulating B. anthracis, PrkC imprints phenotypic memory that facilitates the germination process.
Keyphrases
  • protein kinase
  • induced apoptosis
  • cell cycle arrest
  • poor prognosis
  • single cell
  • cell death
  • multiple sclerosis
  • cell therapy
  • oxidative stress
  • ms ms
  • signaling pathway
  • mass spectrometry
  • cell proliferation