Compaction of isolated Escherichia coli nucleoids: Polymer and H-NS protein synergetics

J Struct Biol. 2016 Apr;194(1):129-37. doi: 10.1016/j.jsb.2016.02.009. Epub 2016 Feb 8.

Abstract

Escherichia coli nucleoids were compacted by the inert polymer polyethylene glycol (PEG) in the presence of the H-NS protein. The protein by itself appears to have little impact on the size of the nucleoids as determined by fluorescent microscopy. However, it has a significant impact on the nucleoidal collapse by PEG. This is quantitatively explained by assuming the H-NS protein enhances the effective diameter of the DNA helix leading to an increase in the depletion forces induced by the PEG. Ultimately, however, the free energy of the nucleoid itself turns out to be independent of the H-NS concentration. This is because the enhancement of the supercoil excluded volume is negligible. The experiments on the nucleoids are corroborated by dynamic light scattering and EMSA analyses performed on DNA plasmids in the presence of PEG and H-NS.

Keywords: Dynamic light scattering; EMSA; Escherichia coli; H-NS protein; Nucleoid; Polyethylene glycol; Polymer physics; Supercoiling.

MeSH terms

  • Algorithms
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics
  • DNA, Bacterial / metabolism*
  • Escherichia coli / chemistry
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism*
  • Fimbriae Proteins / chemistry
  • Fimbriae Proteins / genetics
  • Fimbriae Proteins / metabolism*
  • Kinetics
  • Microscopy, Fluorescence
  • Plasmids / chemistry
  • Plasmids / genetics
  • Plasmids / metabolism
  • Polyethylene Glycols / chemistry
  • Polyethylene Glycols / metabolism
  • Polymers / chemistry
  • Polymers / metabolism*
  • Protein Binding

Substances

  • DNA, Bacterial
  • Escherichia coli Proteins
  • FimG protein, E coli
  • Polymers
  • Fimbriae Proteins
  • Polyethylene Glycols