ydfD encodes a novel lytic protein in Escherichia coli

FEMS Microbiol Lett. 2016 Mar;363(6):fnw039. doi: 10.1093/femsle/fnw039. Epub 2016 Feb 16.

Abstract

Bacteria carry a number of genes that cause cell growth arrest or cell lysis upon expression. Notably, defective prophages retain many lysis proteins. Here, we identified a novel lytic gene, ydfD, on the Qin prophage segment of the Escherichia coli genome. YdfD lyses 99.9% of cells within 2 h of its induction. The co-expression of the upstream gene, dicB, encoding a cell division inhibitor, as well as sulA, encoding another cell division inhibitor, abolished YdfD-induced cell lysis. These results imply that YdfD-induced lysis is a cell division-dependent event. We further found that by deleting the hydrophobic 22-residue N-terminal domain, the resulting 42-residue C-terminal domain was still toxic to cause cell lysis. We propose that YdfD, associated with the cytoplasmic membrane, inhibits an essential cellular process(s).

Keywords: Escherichia coli; YdfD; lysis; prophage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacteriolysis / genetics*
  • Bacteriophages / physiology
  • Escherichia coli / genetics*
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / genetics*
  • Gene Expression Regulation, Bacterial
  • Operon
  • Protein Binding
  • Protein Interaction Domains and Motifs / genetics
  • Protein Multimerization

Substances

  • Escherichia coli Proteins