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Trehalose metabolism in Saccharomyces cerevisiae during heat-shock.

Abstract
When different strains of Saccharomyces cerevisiae grown at 23 degrees C were transferred to 36 degrees C, trehalose and glycogen were accumulated. Glycogen accumulation was less extensive and its synthesis started at least 15 min after initiation of trehalose synthesis. The steady-state intracellular concentration of trehalose increased simultaneously with the activities of the enzymes trehalose-6P synthase, UDPG-pyrophosphorylase, phosphoglucomutase and trehalase. A small but significant change was observed in hexokinase activity. Our results directly implicate isoform PII of hexokinase and the minor isoform of phosphoglucomutase in the pathway of trehalose formation during heat-shock. We also showed that the major isoform of phosphoglucomutase increased in activity but was not essential for trehalose accumulation. Studies with the glucose uptake system indicated that trehalose accumulation could be primarily determined by intracellular availability of substrates due to the increase in the rate of glucose uptake. The increased uptake appears to have two components: a kinetic effect of temperature upon glucose transporters and an increase in the numbers of molecules of the transporters, probably mediated by synthesis de novo.
AuthorsM J Ribeiro, J T Silva, A D Panek
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 1200 Issue 2 Pg. 139-47 (Jul 06 1994) ISSN: 0006-3002 [Print] Netherlands
PMID8031833 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Trehalose
  • Glucosyltransferases
  • trehalose-6-phosphate synthase
  • Hexokinase
  • UTP-Glucose-1-Phosphate Uridylyltransferase
  • Trehalase
  • Phosphoglucomutase
Topics
  • Glucosyltransferases (metabolism)
  • Hexokinase (metabolism)
  • Hot Temperature
  • Models, Chemical
  • Phosphoglucomutase (metabolism)
  • Saccharomyces cerevisiae (metabolism)
  • Trehalase (metabolism)
  • Trehalose (metabolism)
  • UTP-Glucose-1-Phosphate Uridylyltransferase (metabolism)

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