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Saccharomyces cerevisiae culture

Bely, M., Stoeckle, P., Masneuf-Pomarede, I., Dubourdieu, D. (2008) Impact of mixed Torulas-pora ddhmeddi-Saccharomyces cerevisiae culture on high-sugar fermentation. International Journal of Food Microbiology, 122, 312-320. [Pg.375]

White, C., and Gadd, G. M. (1986). Uptake and cellular distribution of copper, cobalt and cadmium in strains of Saccharomyces cerevisiae cultured on elevated concentrations of these metals. FEMS Microbiol. Ecol. 38, 277-283. [Pg.95]

Visser W, Van der Baan AA, Batenburg-van der Vegte W, Scheffers WA, Kramer R, van Dijken JP. Involvement of mitochondria in the assimilatory metabolism of anaerobic Saccharomyces cerevisiae cultures. Microbiology 1994 140 3039-3046. [Pg.44]

Lesmeister, K.E., Heinrichs, A.J., and Gabler, M.T. (2004) Effects of supplemental yeast (Saccharomyces cerevisiae) culture on rumen development, growth characteristics, and blood parameters in neonatal dairy calves. J Dairy Sci... [Pg.156]

Saccharomyces cerevisiae is anaerobically grown in a continuous culture at 30°C. Glucose is used as substrate and ammonia as nitrogen source. A mixture of glycerol and ethanol is produced. At steady-state condition mass the flow rate is stated. The following reaction is proposed for the related bioprocess 4,6... [Pg.230]

Seed culture of Saccharomyces cerevisiae (ATCC 24860) is grown in a rich medium comprising of 1 g glucose, 0.1 g peptone and yeast extract, 0.33 g KH2P04 and 0.03 g Na2HP04 in 100 ml distilled water. The media will be autoclaved at 126 °C and 15 psig for 20 min. The stock culture from ATCC media is transferred to a prepared seed culture. The pH of... [Pg.255]

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]

Kluiyama H. Slaughter J.C. (1995) Control of cell morphology of die yeast Saccharomyces cerevisiae by nutrient limitation in continuous culture. LettApplMicrobiol, 20, 37-40. [Pg.52]

Petersson S, Hansen M W, Axberg K, Hult K and Schnurer J (1998), Ochratoxin A accumulation in cultures of Penicillium verrucosum with the antagonistic yeast Pichia anomala and Saccharomyces cerevisiae , Mycol. Res., 102, 1003-1008. [Pg.389]

There are two yeast expression hosts that have an established track record for high-level production of heterologous proteins, namely Saccharomyces cerevisiae and Pichia pastoris. HTP expression screening using microplate formats has been reported for both these yeasts by Lang and coworkers (Holz et ah, 2002, 2003 Boettner et ah, 2002). In both cases standard protocols have been miniaturized with cells cultured in either 1.5 ml cultures in 96-deep-well plates for S. cerevisiae or 2 ml cultures in 24-deep-well plates for P. pastoris. Soluble... [Pg.32]

While most appfications were performed in suspended cell cultures some authors showed that the application of NADH-dependent fluorescence monitoring is also possible in immobifized cell systems. Here the growth of Clostridium acetobutylicum and the Saccharomyces cerevisiae immobilized in different calcium alginate structures was studied. However, calibration of the culture fluorescence signal with the biomass concentration was not possible but qualitatively an increasing biomass also led to an increase in the fluorescence signals. [Pg.26]

Saccharomyces cerevisiae JDl, mitotic gene conversion in stationary and log-phase cultures... [Pg.370]


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See also in sourсe #XX -- [ Pg.539 ]




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