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Synthetic Products
D-ribo-Phytosphingosine -1-Phosphate
Purity >98%
Product
MW
Catalog
Number
D-ribo-Phytophingosine-1-phosphate
397.49
860491
Stability 1 year
Storage -20°C

Our knowledge of sphingolipid metabolism and function in Saccharomyces cerevisiae is growing rapidly. Dickson & Lester discuss the current status of sphingolipid metabolism including recent evidence suggesting that exogenous sphingoid long-chain bases must first be phosphorylated and then dephosphorylated before incorporation into ceramide. Phenotypes of strains defective in sphingolipid metabolism are discussed because they provide hints about the undiscovered functions of sphingolipids and are one of the major reasons for studying this model eukaryote. The long-chain base phosphates, dihydrosphingosine-1-phosphate and phytosphingosine-1-phosphate, have been hypothesized to play roles in heat stress resistance, perhaps acting as signaling molecules. They evaluate the data supporting this hypothesis and suggest future experiments needed to verify it. Finally, they discuss recent clues that may help to reveal how sphingolipid synthesis and total cellular sphingolipid content are regulated. Sphingolipid long-chain bases and their phosphorylated derivatives, for example, sphingosine-1-phosphate in mammals, have been implicated as signaling molecules. The possibility that Saccharomyces cerevisiae cells also use long-chain-base phosphates to regulate cellular processes has only recently begun to be examined. Skrzypek, Nagiec, et al. present a simple and sensitive procedure for analyzing and quantifying long-chain- base phosphates in S. cerevisiae cells. These data show for the first time that phytosphingosine-1-phosphate (PHS-1-P) is present at a low but detectable level in cells grown on a fermentable carbon source at 25oC, while dihydrosphingosine-1-phosphate (DHS-1-P) is only barely detectable. Shifting cells to 37oC causes transient eight- and fivefold increases in levels of PHS-1-P and DHS-1-P, respectively, which peak after about 10 min. The amounts of both compounds return to the unstressed levels by 20min after the temperature shift. These data are consistent with PHS-1-P and DHS-1-P being signaling molecules. Cells unable to break down long-chain-base phosphates, due to deletion of DPL1 and LCB3, show a 500-fold increase in PHS-1-P and DHS-1-P levels, grow slowly, and survive a 44oC heat stress 10-fold better than parental cells. These and other data for dpl1 or lcb3 single-mutant strains suggest that DHS-1-P and/or PHS-1-P act as signals for resistance to heat stress. Their procedure should expedite experiments to determine how the synthesis and breakdown of these compounds is regulated and how the compounds mediate resistance to elevated temperature.

References:

  1. Dickson, R.C. and R.L. Lester. (1999) Metabolism and selected functions of sphingolipids in the yeast Saccharomyces cerevisiae. Biochim Biophys Acta 1438:305-21.

  2. Skrzypek, M.S., M.M. Nagiec, R.L. Lester, and R.C. Dickson.(1999) Analysis of phosphorylated sphingolipid long-chain bases reveals potential roles in heat stress and growth control in Saccharomyces. J Bacteriol 181:1134-40.
 
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