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Reconstruction of ethanol fermentation in permeabilized cells of the yeast Saccharomyces cerevisiae
Affiliation:1. School of Civil and Transportation Engineering, Guangdong University of Technology, Guangzhou 510006, China;2. Department of Harbor Engineering, Guangzhou Maritime Institute, Guangzhou 510725, China;1. Pro-Science GmbH, Ettlingen, Germany;2. SIMAPS GmbH, Jockgrim, Germany;3. Karlsruhe Institute of Technology, Karlsruhe, Germany;4. POSCO Engineering & Construction, Republic of Korea
Abstract:Saccharomyces cerevisiae cells from a stationary culture were permeabilized with 1% toluene, 4% ethanol and 0.075% Triton X-100. Not only sugars but also ATP, NAD+, magnesium and inorganic phosphate must be simultaneously added to initiate the ethanol fermentation. The optimal pH for the fermentation was between 6.9 to 7.0. Sucrose was a better substrate than glucose. Ethanol fermentation was greatly stimulated by the addition of 1 mM arsenate. Under this condition, permeabilized cells continued to produce ethanol for more than one hour at the rate of 0.141 mmol ethanol/min/mg protein. Methanol inhibited the fermentation with intact cells but did not inhibit the one using permeabilized cells. In contrast, propanol inhibited fermentations both with intact and permeabilized cells.
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