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Browsing by Subject "Fermentation"

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    Effect of culture conditions on the competition between lactate oxidisers and fermenters in a biological sulfate reduction system
    (Elsevier, 2012) Oyekola, Oluwaseun O; Harrison, Susan T L; van Hille, Robert P
    Kinetic constants (μmax and Ks) describing the predominance of lactate oxidation and fermentation were determined in chemostat cultures. The kinetics of sulfate reduction and lactate utilization were determined from 0.5 to 5 d residence times at feed sulfate concentrations of 1.0–10.0 g l−1. The kinetics of lactate fermentation in the absence of sulfate were investigated at residence times of 0.5–5 d. The lactate oxidizers (LO) were characterized by a μmax of 0.2 h−1 and Ks value of 0.6 g l−1 compared with a μmax of 0.3 h−1 and Ks of 3.3 g l−1 for the lactate fermenters (LF). Using mathematical models, it was shown that LO competed more effectively for lactate at low lactate concentrations (⩽5 g l−1) and high sulfide concentrations (0.5 g l−1). Lactate fermenters outcompeted the oxidizers under conditions of excess lactate (>5 g l−1) and low sulfide (0.014–0.088 g l−1).
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    Effect of culture conditions on the competitive interaction between lactate oxidizers and fermenters in a biological sulfate reduction system
    (Elsevier, 2012) Oyekola, Oluwaseun O; Harrison, Susan T L; Van Hille, Robert P
    Kinetic constants (lmax and Ks) describing the predominance of lactate oxidation and fermentation were determined in chemostat cultures. The kinetics of sulfate reduction and lactate utilization were determined from 0.5 to 5 d residence times at feed sulfate concentrations of 1.0–10.0 g l1 . The kinetics of lactate fermentation in the absence of sulfate were investigated at residence times of 0.5–5 d. The lactate oxidizers (LO) were characterized by a lmax of 0.2 h1 and Ks value of 0.6 g l1 compared with a lmax of 0.3 h1 and Ks of 3.3 g l1 for the lactate fermenters (LF). Using mathematical models, it was shown that LO competed more effectively for lactate at low lactate concentrations (65gl1 ) and high sulfide concentrations (0.5 g l1 ). Lactate fermenters outcompeted the oxidizers under conditions of excess lactate (>5 g l1 ) and low sulfide (0.014–0.088 g l1 ). 2011 E
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    Modelling of batch and fed-batch ethanol fermentation
    (1989) Glyn, Julian E H; Hansford, Geoffrey Spearing
    Two series of batch and fed-batch fermentations were carried out using S.cerevisiae in a semi-defined medium containing 200 gl-1 glucose as limiting substrate. Growth rates were calculated and the data used to test the applicability of eight empirical kinetic models. The form proposed by Levenspiel, combining the concept of a limiting ethanol concentration with a power-law form, gave the best results with these data. Glucose concentration was found to have a far smaller, though not negligible, effect on growth rate under these conditions. It was also observed that in fed-batch fermentations the total substrate uptake rate of the broth became constant soon after commencement of feeding, without cessation of growth. It is suggested that ethanol inhibits the synthesis of a rate-controlling enzyme in the glycolyti·c chain, but no previous work could be found to support or refute this explanation. A quasi-mechanistic model of growth under the condition of constant substrate consumption rate is formulated and discussed.
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    Molecular analysis and regulation of the Clostridium acetobutylicum glutamine synthetase gene glnA cloned in Escherichia coli
    (1990) Janssen, Paul J D; Woods, D R
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    A reassessment of the production of acetone and butanol by Clostridium acetobutylicum in continuous culture
    (1987) Clarke, Kim Gail; Hansford, Geoffrey Spearing; Jones, David T
    The production of acetone and butanol by Clostridium acetobutylicum P 262 was studied in continuous culture under conditions where the nutrients were present in excess of the requirements and the cell growth was limited by the products formed during the fermentation. This system differs from most continuous culture systems used to obtain solvent production where the limitation of a specific nutrient was utilised to limit the cell growth.
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