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Genetic analysis Saccharomyces cerevisiae

Knowledge of the life cycle and genetics of Saccharomyces cerevisiae has been obtained using strains selected for their suitability for analysis. Such strains, often termed laboratory or genetic , have their origins in commercially used bakers yeast. [Pg.166]

Kennedy B.K. Guarente L. (1996) Genetic analysis of aging in Saccharomyces cerevisiae. Trends Genet, 12, 355-359. [Pg.52]

Several lines of evidence indicate that CENP-A replaces conventional H3 in the nucleosome. Biochemical studies showed that CENP-A co-sediments with nucleo-some core particles [7] and a genetic analysis indicates an interaction between Cse4p, the CENP-A of Saccharomyces cerevisiae, and H4 [16,17]. A recent study with CENP-A purified from HeLa cells or expressed in bacteria showed that it can substitute for conventional H3 in nucleosome reconstitution [18]. Reconstituted CENP-A-containing nucleosomes appear to contain the other core histones in appropriate stoichiometry. However, they did not strongly protect 146 bp of core DNA from micrococcal nuclease, suggesting that CENP-A may significantly alter some aspects of the core nucleosome structure. [Pg.183]

ZamboneUi, C., MutineUi, P., Pacchetti, G. (1975) Biosynthesis of sulphur amino acids in Saccharomyces cerevisiae. I. Genetic analysis of leaky mutants of sulphite reductase. Archives of Microbiology, 102, 247-251. [Pg.392]

Mackay, V., and Manney, T.R. (1974). Mutations affecting sexual conjugation and related processes in Saccharomyces cerevisiae. II. Genetic analysis of nonmating mutants. Genetics 76 273-288. [Pg.86]

For much work on chemical activities of micro-organisms, it is important to use strains having known relevant genetical characteristics. Unfortunately, however, strains of only two species, Saccharomyces cerevisiae and Schizosaccharomyces pombe, have as yet been subjected to extensive genetic analysis, and neither species can utilize a wide range of exogenous sugars. [Pg.137]

Barnes, C., Hansen, W. J., Holcomb, C. L., and Rine, J. (1984). Asparagine-linked glycosylation in Saccharomyces cerevisiae Genetic analysis of an early step. Mol. Cell Biol. 4, 2381-2388. [Pg.380]

Saccharomyces cerevisiae played an important role in the genetic analysis of riboflavin biosynthesis. Mating analysis between riboflavin auxotrophic mutants obtained by random mutagenesis and screening of haploid... [Pg.120]

The plasma membrane H+-ATPase from Saccharomyces cerevisiae is a highly electrogenic proton pump that maintains cellular membrane potentials in excess of — 200 mV. This enzyme is used as a model system to probe the mechanism of electrogenic proton transport because it is readily amenable to genetic, biochemical, and biophysical analysis. The H+-ATPase plays an essential role in intracellular pH regulation and maintenance of electrochemi-... [Pg.315]

Gallego, F. J., Perez, M. A., Nunez, Y., Hildago, P. (2005). Comparison of RAPDs, AFLPs and SSR marker for genetic analysis of yeast strains of Saccharomyces cerevisiae. Food... [Pg.466]

Van Vuuren H.J.J., Viljoen M., Grobler J., Volschenk H., Bauer F. and Subden R.E., 1996, Genetic analysis of the Schizosaccharomyces pombe malate permeases, Mael and malic enzyme, MaeU, genes and their expression in Saccharomyces cerevisiae, in (Enolo-gie 95, 5 Symposium international d cenologie, p. 195-197, A. Lonvaud, Tech et Doc, Paris. [Pg.78]

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See also in sourсe #XX -- [ Pg.146 , Pg.147 , Pg.148 , Pg.149 , Pg.150 , Pg.151 , Pg.152 , Pg.153 , Pg.154 ]



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