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Bacterial growth is closely tied to nutrient availability, with cells proliferating exponentially under favorable conditions and entering a stationary phase when resources become scarce. This transition is mediated by a regulatory mechanism known as the stringent response, which allows bacteria to adapt to nutrient deprivation by modulating gene expression and metabolic activity.During nutrient scarcity, intracellular amino acid levels decline. It results in the accumulation of uncharged tRNAs...
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Related Experiment Video

Updated: Aug 17, 2025

Monitoring Intraspecies Competition in a Bacterial Cell Population by Cocultivation of Fluorescently Labelled Strains
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Magnesium Modulates Bacillus subtilis Cell Division Frequency.

Tingfeng Guo1, Jennifer K Herman1

  • 1Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA.

Journal of Bacteriology
|December 14, 2022
PubMed
Summary
This summary is machine-generated.

Extracellular magnesium (Mg2+) availability can alter Bacillus subtilis cell division frequency without impacting growth rate. This discovery offers new avenues for understanding the signals that regulate bacterial cell division.

Keywords:
BacillusLBSigBUppScell divisionmagnesiummanganesemorphologyundecaprenylzinc

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Area of Science:

  • Microbiology
  • Cell Biology
  • Biochemistry

Background:

  • Cell division signals in microorganisms remain largely unknown.
  • Bacterial cell division is often considered intrinsic to the cell cycle.
  • Microorganisms can skip cell division rounds while continuing to grow and replicate DNA.

Purpose of the Study:

  • To investigate the role of extracellular magnesium (Mg2+) availability in modulating bacterial cell division frequency.
  • To determine if Mg2+ concentration can uncouple bacterial growth rate from cell division frequency.
  • To identify transcriptional changes associated with altered cell division.

Main Methods:

  • Culturing Bacillus subtilis under varying extracellular magnesium (Mg2+) concentrations.
  • Measuring cell length, growth rate, and division frequency.
  • Utilizing a riboswitch reporter to assess intracellular Mg2+ levels.
  • Analyzing gene expression changes using transcriptomic analysis (SigB, Fur, MntR, Zur regulons).

Main Results:

  • A specific window of extracellular Mg2+ availability shortened Bacillus subtilis cells without affecting growth rate.
  • Cell length reduction was proportional to increasing Mg2+ concentration (0.2–4.0 mM).
  • Excess Mg2+ led to increased cell division frequency, indicated by more FtsZ-rings per unit cell length and enhanced expression of stress-response and metal-uptake related genes.

Conclusions:

  • Extracellular Mg2+ concentration is a critical regulator that can uncouple bacterial growth rate from cell division frequency.
  • The study identifies Mg2+ as a potential signal for triggering cell division.
  • Findings suggest cell division is linked to the general stress response and demands for metal ion homeostasis.