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Saccharomyces cerevisiae cells

Hartwell L.H. (1974) Saccharomyces cerevisiae cell cycle. BacteriolRev, 38, 164-198. [Pg.51]

Pringle J.R. Hartwell L.H. (1981) The Saccharomyces cerevisiae cell cycle. In The Molecular Biology of the Yeast Saccharomyces, vol. 1. Life Cycle and Inheritance (eds J.N. Strathem, E.W. Jones J.R. Broach), pp. 97-142. Cold Spring Harbor, NY Cold Spring Harbor Laboratory. [Pg.52]

To study the specific regulation of the synthesis of NCR-sensitive amino acid transporters, Saccharomyces cerevisiae cells are grown with proline or urea as the sole source of nitrogen, i.e., in the absence of NCR (see section 6.3). [Pg.234]

The two hepatitis B vaccines available in the United States are Recombivax HB and Engerix-B. These vaccines are produced with recombinant DNA technology by inserting the gene for HBsAg into the plasmid that is synthesized by Saccharomyces cerevisiae cells. Both vaccines are effective in providing... [Pg.352]

Pardo M et al. A proteomic approach for the study of Saccharomyces cerevisiae cell wall biogenesis. Electrophoresis 2000 21 3396-3410. [Pg.121]

Ramalho PA, Paiva S, Cavaco-Paulo A et al (2005) Azo reductase activity of intact Saccharomyces cerevisiae cells is dependent on the Frelp component of plasma membrane ferric reductase. Appl Environ Microbiol 71 3882-3888... [Pg.191]

Ito, T. Ito, A. Hieda, K. Kobayashi, K. Wavelength dependence of inactivation and membrane damage to Saccharomyces cerevisiae cells by monochromatic synchrotron vacuum-uv radiation (145-190 nm). Radiat Res. 1983, 96 (3), 532-548. [Pg.488]

Johnston, L.H. Nasmyth, K.A. (1978). Saccharomyces cerevisiae cell cycle mutant cdc9 is defective in DNA ligase. Nature (London) 274, 891-893. [Pg.147]

Hottinger, T., T. Boiler, and A. Wiemken (1987). Rapid changes of heat and desiccation tolerance correlated with changes of trehalose content in Saccharomyces cerevisiae cells subjected to temperature shifts. FEBS Lett. 220 113-115. [Pg.443]

Fig. 2. Saccharomyces cerevisiae cells observed by phase-contrast microscopy (a) and Streptomyces ambofaciens filament observed by epifluorescence microscopy (after Propidium Iodide staining) (b)... Fig. 2. Saccharomyces cerevisiae cells observed by phase-contrast microscopy (a) and Streptomyces ambofaciens filament observed by epifluorescence microscopy (after Propidium Iodide staining) (b)...
Fig. 5. a In-situ microscope proposed by Bittner et al. b Saccharomyces cerevisiae cells observed by in-situ microscopy in function of culture time (by permission of T. Schepper)... [Pg.141]

Fig. 28. Vacuole of Saccharomyces cerevisiae cell observed by phase-contrast microscopy... Fig. 28. Vacuole of Saccharomyces cerevisiae cell observed by phase-contrast microscopy...
Figure 8.21 The content of different PolyP fractions in Saccharomyces cerevisiae cells in the process of growth after re-inoculation of late-logarithmic cells on the fresh medium with a high initial culture density (a) re-inoculation from a P -limited medium (with 1 mM P ) to a complete Reader medium (with 18 mM P ) (b) re-inoculation from a complete Reader medium to a fresh one (o) polyP(I) (A) polyP(II) ( ) polyP(III) (a) polyP(IV) (x) polyP(V). The growth curves are shown below in Figure 8.23(c). Figure 8.21 The content of different PolyP fractions in Saccharomyces cerevisiae cells in the process of growth after re-inoculation of late-logarithmic cells on the fresh medium with a high initial culture density (a) re-inoculation from a P -limited medium (with 1 mM P ) to a complete Reader medium (with 18 mM P ) (b) re-inoculation from a complete Reader medium to a fresh one (o) polyP(I) (A) polyP(II) ( ) polyP(III) (a) polyP(IV) (x) polyP(V). The growth curves are shown below in Figure 8.23(c).
Figure 8.24 The effect of inhibitors on the content of certain PolyP fractions in Saccharomyces cerevisiae cells under phosphate overplus (Trilisenko et al., 2003). (A) PolyP in Pj-starved cells (B-G) PolyP in cells grown at 2 h after re-inoculation on the complete medium (phosphate overplus) (B) control conditions (C) 10 mg mT1 of cycloheximide (D) 10 //M FCCP (E) 20 //M FCCP (F) 250 /-iM iodacetamide (G) 50 nM bafilomycin A. PolyP fractions (1) PolyP(I) (2) PolyP(H) (3) PolyP(III) (4) PolyP(IV) (5) PolyP(V). Figure 8.24 The effect of inhibitors on the content of certain PolyP fractions in Saccharomyces cerevisiae cells under phosphate overplus (Trilisenko et al., 2003). (A) PolyP in Pj-starved cells (B-G) PolyP in cells grown at 2 h after re-inoculation on the complete medium (phosphate overplus) (B) control conditions (C) 10 mg mT1 of cycloheximide (D) 10 //M FCCP (E) 20 //M FCCP (F) 250 /-iM iodacetamide (G) 50 nM bafilomycin A. PolyP fractions (1) PolyP(I) (2) PolyP(H) (3) PolyP(III) (4) PolyP(IV) (5) PolyP(V).
N. A. Andreeva and L. A. Okorokov (1993). Purification and characterization of highly active and stable polyphosphatase from Saccharomyces cerevisiae cell envelope. Yeast, 9, 127-139. [Pg.211]

C. A. Ponce de Leon, M. Montes-Bayon, C. Paquin, J. A. Caruso, Selenium incorporation into Saccharomyces cerevisiae cells a study of different incorporation methods, J. Appl. Microbiol., 92 (2002), 602D610. [Pg.698]

Rossi-Alva, J. C., and Miguez Rocha-Leao, M. H. (2003), A strategic study using mutant-strain entrapment in calcium alginate for the production of Saccharomyces cerevisiae cells with high invertase activity, Biotechnol. Appl. Biochem., 38,43-51. [Pg.589]

Levin, D.E., Bowers, B., Chen, C.Y., Kamada, Y., and Watanabe, M., 1994, Dissecting the protein kinase C/MAP kinase signalling pathway of Saccharomyces cerevisiae. Cell. Mol. Biol. Res. 40 229-239. [Pg.153]

Bardi, L., Cocito, C., Marzona, M. (1999) Saccharomyces cerevisiae cell fatty acid composition and release during fermentation without aeration and in absence of exogenous lipids. International Journal of Food Microbiology, 47, 133-140. [Pg.375]

Figure 4 Progress of the specimen temperature during the drying of Saccharomyces cerevisiae cells at room temperature (20°C). (From Ref. 24.)... Figure 4 Progress of the specimen temperature during the drying of Saccharomyces cerevisiae cells at room temperature (20°C). (From Ref. 24.)...
Investigation of a partially purified particulate gluean preparation from Saccharomyces cerevisiae cell walls has expanded. Glucan is held re-sponsil le for most of the reticuloendothelial-stimulating properties of zymosan. The preparation was reported to activate macrophages as assessed by... [Pg.151]

Hepatitis B (recombinant) Vaccine is a noninfectious rDNA hepatitis B vaccine containing purified surface antigen of the virus obtained by culturing genetically engineered Saccharomyces cerevisiae cells, which carry the surface antigen gene of the hepatitis B... [Pg.341]

His, K., Hinzpeter, A., Edelman, A., and Kurlandzka, A. (2005) The functioning of mammalian CIC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Khalp. Biochem. J. 390, 655-664. [Pg.461]

K.S. Seo, K.H. Choo, H.N. Chang, J.K. Park, A flow injection analysis system with encapsulated high-density Saccharomyces cerevisiae cells for rapid determination of biochemical oxygen demand, Appl. Microbiol. Biotechnol. 83 (2009) 217. [Pg.425]

Since the cofactors are not essential in S. cerevisiae, but the tubulin heterodimer is, it is clear that tubulin in this organism must be able to form heterodimers in the absence of cofactors. One possible explanation for this is that the sequences of the S. cerevisiae tubulins are the most divergent known. Saccharomyces cerevisiae cells contain only relatively simple microtubule arrays that participate in only three well defined and temporally distinct cellular process mitosis, meiosis, and nuclear fusion. Perhaps this reduced selective pressure on their tubulin genes has allowed the evolution of spontaneously dimerizing tubulin in this organism. [Pg.97]

TerBush, D. R., and Novick, P. (1995). Sec6, Sec8, and Secl5 are components of a multisubunit complex which localizes to small bud tips in Saccharomyces cerevisiae.]. Cell... [Pg.389]

Somolinos, M., Garcia, D., Condon, S., Manas, P., and Pagan, R. 2008a. Biosynthetic requirements for the repair of sublethally injured Saccharomyces cerevisiae cells after pulsed electric fields. Journal of Applied Microbiology 105 166-174. [Pg.216]

Dorer, R., Pryciak, P. M., and Hartwell, L. H. (1995) Saccharomyces cerevisiae cells execute a default pathway to select a mate in the absence of pheromone gradients. J. Cell Biol. 131, 845-861. [Pg.109]

Guillou S, Besnard V, Murr NE, Eederighi M. (2003). Viability of Saccharomyces cerevisiae cells exposed to low-amperage electrolysis as assessed by staining procedure and ATP content. International Journal of Food Microbiology 88 85-89. [Pg.382]


See other pages where Saccharomyces cerevisiae cells is mentioned: [Pg.79]    [Pg.198]    [Pg.128]    [Pg.245]    [Pg.557]    [Pg.269]    [Pg.275]    [Pg.181]    [Pg.203]    [Pg.136]    [Pg.140]    [Pg.144]    [Pg.153]    [Pg.171]    [Pg.254]    [Pg.228]    [Pg.423]    [Pg.52]    [Pg.568]    [Pg.272]   
See also in sourсe #XX -- [ Pg.216 ]




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Cell division cycle, Saccharomyces cerevisiae

Cerevisiae

Saccharomyces cerevisia

Saccharomyces cerevisiae

Saccharomyces cerevisiae cell ageing

Saccharomyces cerevisiae cell disruption

Saccharomyces cerevisiae cell factory

Saccharomyces cerevisiae cell wall

Saccharomyces cerevisiae cell wall structure

Whole cells Saccharomyces cerevisiae

Yeast Saccharomyces cerevisiae Cells

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