Motility behavior of rpoS-deficient Escherichia coli analyzed by individual cell tracking

J Biosci Bioeng. 2012 Dec;114(6):652-6. doi: 10.1016/j.jbiosc.2012.06.014. Epub 2012 Jul 29.

Abstract

Motility is one of the most extensively studied cellular events conducted by bacteria, including Escherichia coli. A motility agar plate assay showed that deletion of the rpoS gene enhanced the apparent motility of the E. coli BW25113 strain, which inherently had negligible motility compared to wild-type E. coli strains, such as MG1655, with no effect on cell growth. This enhancement of motility was accompanied by drastic up-regulation of genes involved in the formation and rotation of flagella. Furthermore, an individual cell motility assay showed that the population of ΔrpoS cells had bimodal motility character, and that a minority of this population exhibited a much higher motility rate. These results support a view that a minority population contributes to increasing in apparent motility of the whole population of ΔrpoS cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Biological Assay
  • Cell Tracking
  • Escherichia coli / cytology*
  • Escherichia coli / genetics
  • Escherichia coli / growth & development
  • Escherichia coli / physiology*
  • Escherichia coli Proteins / genetics
  • Flagella / genetics
  • Flagella / physiology
  • Gene Deletion
  • Gene Expression Regulation, Bacterial
  • Movement*
  • Sigma Factor / deficiency*
  • Sigma Factor / genetics
  • Up-Regulation

Substances

  • Bacterial Proteins
  • Escherichia coli Proteins
  • Sigma Factor
  • sigma factor KatF protein, Bacteria