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Regulation of cellular Mg2+ by Saccharomyces cerevisiae

Troy Beeler*, Kerry Bruce, Teresa Dunn

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Regulation of cellular Mg2+ by S. cerevisiae was investigated. The minimal concentration of Mg2+ that results in optimal growth of S. cerevisiae is about 30 μM and a half-maximum growth rate is attained at about 5 μM Mg2+. Since the plasma membrane has an electrical potential greater than 100 mV, passive equilibration of Mg2+ across the plasma membrane would provide sufficient cytosolic Mg2+ (0.1-1 mM). The total cellular Mg2+ of cells grown in synthetic medium containing 1 mM Mg2+ is about 400 nmol/mg protein, most of which is bound to polyphosphate, nucleic acids, and ATP. Total cellular Mg2+ decreases to about 80 nmol/mg protein as the Mg2+ in synthetic-growth medium is reduced to 0.02 mM, but remains relatively constant in growth medium containing 1 to 100 mM Mg2+. Cells shifted into Mg2+-free medium continue to grow by utilizing the vacuolar Mg2+ stores. Mg2+-starved cells replenish vacuolar Mg2+ stores with a halftime of 30 min. following the addition of 1 mM Mg2+ to the growth medium. The data indicate that cytosolic Mg2+ is maintained by the regulation of Mg2+ fluxes across both the vacuolar and plasma membranes.

Original languageEnglish
Pages (from-to)310-318
Number of pages9
JournalBiochimica et Biophysica Acta - Biomembranes
Volume1323
Issue number2
DOIs
StatePublished - 31 Jan 1997

Keywords

  • Calcium
  • Dichlorophosphonazo III
  • Magnesium
  • Polyphosphate
  • S. cerevisiae
  • Vacuole

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