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Saccharomyces cerevisiae sphingolipids

Molecular targets have been elucidated for Dm-AMPl and Rs-AFP2. Dm-AMPl was found to bind plasma membranes from Neurospora crassa and Saccharomyces cerevisiae in a saturable manner and it competed with closely related defensins for binding. Mutational studies with S. cerevisiae identified lipid raffs containing sphingolipids as a molecular target " while glycosylphosphatidylinositol (GPI)-anchored proteins could be... [Pg.263]

Oh C. S., Toke D. A., Mandala S. and Martin C. E. (1997) EL02 and EL03, homologues of the Saccharomyces cerevisiae ELOl gene, function in fatty acid elongation and are required for sphingolipid formation. J. Biol. Chem. 272, 17376-17384. [Pg.250]

Hallstrdm, T.C., Lambert, L., Schorling, S., Balzi, E., Goffeau, A., and Moye-Rowley W.S. (2001) Coordinate control of sphingolipid biosynthesis and multidrug resistance in Saccharomyces cerevisiae. The Journal of Biolt al Chemistry, 276, 23674-23680. [Pg.186]

Alvarez-Vasquez, R, Sims, K.J., Cowart, L.A., Okamoto, Y., Voit, E.O., Hannun, Y.A. 2005. Simulation and validation of modelled sphingolipid metabolism in Saccharomyces cerevisiae. Nature 433 425-430. Hakomori, S. 1983. Chemistry of glycosphingolipids. In Sphingolipid Biochemistry. J.N. Kanfer, S. Hakomori, editors. New York, NY Plenum, pp. 1-164. [Pg.396]

Figure 12.16 Sphingolipid biosynthesis in Pichia ciferrii. Enzymes are shown as ovals and named according to the corresponding homologues from Saccharomyces cerevisiae. Abbreviations AcTR, acetyl-CoA long-chain base acetyltransferase TAPS, tetraacetyl phytosphingosine TriASa, triacetyl sphinganine TriASo, triacetyl sphingosine IP, inositol phosphoryl. TAPS is by far the most abundant sphingolipid formed in wild-t5 e cells, as reflected by the strength of the arrows. Figure 12.16 Sphingolipid biosynthesis in Pichia ciferrii. Enzymes are shown as ovals and named according to the corresponding homologues from Saccharomyces cerevisiae. Abbreviations AcTR, acetyl-CoA long-chain base acetyltransferase TAPS, tetraacetyl phytosphingosine TriASa, triacetyl sphinganine TriASo, triacetyl sphingosine IP, inositol phosphoryl. TAPS is by far the most abundant sphingolipid formed in wild-t5 e cells, as reflected by the strength of the arrows.
Lester, R.L., Wells, G.B., Oxford, G. and Dickson, R.C. (1993) Mutant strains of Saccharomyces cerevisiae lacking sphingolipids synthesize novel inositol glycerophospholipids that mimic sphinglipid structure. J. Biol. Chem. 268 845-856. [Pg.409]

Dickson, RC and Lester, RL (1999) Metabolism and selected functions of sphingolipids in the yeast Saccharomyces cerevisiae. Biochint Biophys Acta, 1438, 305-321. [Pg.161]

Jenkins, GM, Richards, A, Wahl, T, Mao, C, Obeid, L and Hannun, Y (1997) Involvement of yeast sphingolipids in the heat stress response of Saccharomyces cerevisiae. J Biol Chem, 212, 32566-32572. [Pg.162]

Thevissen, K., Francois, I.E., Takemoto, J.Y., Ferket, K.K., Meert, E.M., and Cammue, B.P. (2003b) DmAMPl, an antifungal plant defensin from dahlia (Dahlia merckii), interacts with sphingolipids from Saccharomyces cerevisiae. FEMS Microbiol Lett 226 169-173. [Pg.298]

Guan, X.L. and Wenk, M.R. (2006) Mass spectrometry-based profiling of phospholipids and sphingolipids in extracts from Saccharomyces cerevisiae. Yeast 23, 465-477. [Pg.440]

Abeijon C, Yanagisawa K, Mandon EC, Hausler A, Moremen K, et al. Guanosine diphosphatase is required for protein and sphingolipid glycosylation in the Golgi lumen of Saccharomyces cerevisiae. J. Cell Biol 1993 722 307-323. [Pg.1156]


See other pages where Saccharomyces cerevisiae sphingolipids is mentioned: [Pg.257]    [Pg.131]    [Pg.415]    [Pg.148]    [Pg.156]    [Pg.333]    [Pg.1145]   
See also in sourсe #XX -- [ Pg.449 ]




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