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Saccharomyces cerevisiae, effect

Griac, P., and Henry, S.A., 1996, Phosphatidylcholine biosynthesis in Saccharomyces cerevisiae Effects on regulation of phospholipid synthesis and respiratory competence. In Op den Kamp, J.A.F. (ed.), NATO ASI Series Molecular Dynamics of Biological Membranes. Springer, Verlag, pp. 339-346. [Pg.151]

Kuqan, J. (1985). Alpha-factor structural gene mutations in Saccharomyces cerevisiae effects on alpha-factor production and mating. Mol Cell Biol 5 787-796. [Pg.36]

Owing to diminishing fossil fuel reserves, alternative energy sources need to be renewable, sustainable, efficient, cost-effective, convenient and safe.1 In recent decades, microbial production of ethanol has been considered as an alternative fuel for the future because fossil fuels are depleting. Several microorganisms, including Clostridium sp. and yeast, the well-known ethanol producers Saccharomyces cerevisiae and Zymomonas mobilis, are suitable candidates to produce ethanol.2,3... [Pg.207]

L Vova TS. 1984. [Study of the mutagenic effect of 5 promising pesticides in mouse bone marrow cultured human peripheral blood lymphocytes, and in the yeast Saccharomyces-cerevisiae.] Tsitol Genet 18 455-457. (Russian)... [Pg.304]

Drdak, M. et al., Red beet pigment composition effects of fermentation by different strains of Saccharomyces cerevisiae, J. Food Sci., 57, 935, 1992. [Pg.98]

Feedback inhibition of amino acid transporters by amino acids synthesized by the cells might be responsible for the well known fact that blocking protein synthesis by cycloheximide in Saccharomyces cerevisiae inhibits the uptake of most amino acids [56]. Indeed, under these conditions, endogenous amino acids continue to accumulate. This situation, which precludes studying amino acid transport in yeast in the presence of inhibitors of protein synthesis, is very different from that observed in bacteria, where amino acid uptake is commonly measured in the presence of chloramphenicol in order to isolate the uptake process from further metabolism of accumulated substances. In yeast, when nitrogen starvation rather than cycloheximide is used to block protein synthesis, this leads to very high uptake activity. This fact supports the feedback inhibition interpretation of the observed cycloheximide effect. [Pg.233]

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]

Shu, C. H., and Yang, S. T., Effect of Particle Loading on GM-CSF Production by Saccharomyces cerevisiae in a Three-Phase Fluidized Bed Bioreactor, Biotechnol. Bioeng., 51 229 (19%)... [Pg.678]

Arni P. 1985. Induction of various genetic effects in the yeast Saccharomyces cerevisiae strain D7. In Ashby J, de Serres FJ, et al., eds. Progress in mutation research, Vol. 5. Evaluation of short-term tests for carcinogens. Amsterdam, The Netherlands Elsevier Science Publishers, 217-224. [Pg.98]

Thuroff E, Kaufer NF, Lochmann ER. 1986. Effect of acrylonitrile on the transcription of specific genes in Saccharomyces cerevisiae. Mol Gen Genet 202 336-337. [Pg.120]

In addition to bacterial conversion of L-methionine to cheese aroma compounds, certain cheese-ripening yeasts have been implicated. They include De-baromyces hansenii, Geotrichum candidum, and Yarrowia lipolytica, in addition to Kluyveromyces lactis and Saccharomyces cerevisiae (previously noted). Of these yeasts, Geotrichum candidum was most effective at producing sulfur compounds with the major product being S-methyl thioacetate, with smaller amounts of MT, DMS, DMDS, and DMTS. Kluyveromyces lactis had a similar profile, but produced a much smaller amount of S-methyl thioacetate than did G. candidum. S-Methyl thioacetate is formed by a reaction of MT and acetyl-CoA (Equation 7) ... [Pg.682]

Wei Y, Yu L, Bowen J, Gorovsky MA, Allis CD (1999) Phosphorylation of histone H3 is required for proper chromosome condensation and segregation. Cell 97(1) 99—109 Wyatt HR, Liaw H, Green GR, Lustig AJ (2003) Multiple roles for Saccharomyces cerevisiae histone H2A in telomere position effect, Spt phenotypes and double-strand-break repair. Genetics 164(l) 47-64... [Pg.336]

Simons V et al (2006) Dual effects of plant steroidal alkaloids on Saccharomyces cerevisiae. Antimicrob Agents and Chemother 50 2732... [Pg.29]

Hammer KA, Carson CF, Riley TV. (2004) Antifungal effects of Melaleuca alternifolia (tea tree) oil and its components on Candida albicans, Candida glabrata and Saccharomyces cerevisiae. J Antimicrob Chemother 53 1081-1085. [Pg.516]

Rine, J. and Herskowitz, I. (1987) Four genes responsible for a position effect on expression from HML and HMR in Saccharomyces cerevisiae. Genetics, 116, 9-22. [Pg.236]

DNB on mitotic recombination in Saccharomyces cerevisiae. Doses of up to 32 mg/mL were administered, but no genotoxic effects of any kind were observed either with or without metabolic activation (McGregor et al. 1980). Refer to Table 2-2 for a further summary of the genotoxic effects of 1,3-DNB exposure. [Pg.52]

The yeast Saccharomyces cerevisiae is a useful microbiological alternative to bacteria, especially in the field of photobiology [30-32]. Several endpoints such as colonyforming ability (lethal effects), nuclear and cytoplasmic mutations (reversion due to... [Pg.480]

These optical probes are the most universally applicable in situ devices for on-line biomass monitoring up to now [15,16]. Konstaninov et al. [17] tested several absorbance and scattering sensors for real-time biomass concentration monitoring in mammalian cell cultivation processes and Hatch and Veilleux [18] compared optical density probes with oxygen uptake rates, packed cell volume, and off-line cell mass monitoring in commercial fed-batch fermentations of Saccharomyces cerevisiae [19]. In order to minimize influencing effects, special chemometric data treatment is necessary [20]. [Pg.22]

Alksne LE, Anthony RA, Liebman SW, Warner JR (1993) An accuracy center in the ribosome conserved over 2 billion years. Proc Natl Acad Sci USA 90 9538-9541 Allen KD, Wegrzyn RD, Chernova TA, Muller S, Newnam GP, Winslett PA, Wittich KB, Wilkinson KD, Chernoff YO (2004) Hsp70 chaperones as modulators of prion life cycle novel effects of Ssa and Ssb on the Saccharomyces cerevisiae prion [PS1+]. Genetics 169 1227-1242 All-Robyn JA, Kelley-Geraghty D, Griffin E, Brown N, Liebman SW (1990) Isolation of omnipotent suppressors in an [eta-t] yeast strain. Genetics 124 505-514... [Pg.21]


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