Short-term kinetics of rRNA degradation in Escherichia coli upon starvation for carbon, amino acid or phosphate

Mol Microbiol. 2020 May;113(5):951-963. doi: 10.1111/mmi.14462. Epub 2020 Feb 5.

Abstract

Ribosomes are absolutely essential for growth but are, moreover, energetically costly to produce. Therefore, it is important to adjust the cellular ribosome levels according to the environmental conditions in order to obtain the highest possible growth rate while avoiding energy wastage on excess ribosome biosynthesis. Here we show, by three different methods, that the ribosomal RNA content of Escherichia coli is downregulated within minutes of the removal of an essential nutrient from the growth medium, or after transcription initiation is inhibited. The kinetics of the ribosomal RNA reduction vary depending on which nutrient the cells are starved for. The number of ribosomes per OD unit of cells is roughly halved after 80 min of starvation for isoleucine or phosphate, while the ribosome reduction is less extensive when the cells are starved for glucose. Collectively, the results presented here support the simple model proposed previously, which identifies the inactive ribosomal subunits as the substrates for degradation, since the most substantial rRNA degradation is observed under the starvation conditions that most directly affect the protein synthesis.

Keywords: Escherichia coli; bacterial stress response; nutrient starvation; ribosomal RNA; stable RNA degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism
  • Carbon / metabolism
  • Culture Media
  • Escherichia coli / genetics*
  • Escherichia coli / growth & development*
  • Gene Expression Regulation, Bacterial
  • Gene-Environment Interaction
  • Kinetics
  • Phosphates / metabolism
  • Protein Biosynthesis
  • RNA Stability
  • RNA, Bacterial / chemistry*
  • RNA, Ribosomal / chemistry*
  • Ribosomes / genetics
  • Ribosomes / metabolism

Substances

  • Amino Acids
  • Culture Media
  • Phosphates
  • RNA, Bacterial
  • RNA, Ribosomal
  • Carbon