Literature DB >> 9393686

Glycolytic flux is conditionally correlated with ATP concentration in Saccharomyces cerevisiae: a chemostat study under carbon- or nitrogen-limiting conditions.

C Larsson1, A Nilsson, A Blomberg, L Gustafsson.   

Abstract

Anaerobic and aerobic chemostat cultures of Saccharomyces cerevisiae were performed at a constant dilution rate of 0.10 h(-1). The glucose concentration was kept constant, whereas the nitrogen concentration was gradually decreasing; i.e., the conditions were changed from glucose and energy limitation to nitrogen limitation and energy excess. This experimental setup enabled the glycolytic rate to be separated from the growth rate. There was an extensive uncoupling between anabolic energy requirements and catabolic energy production when the energy source was present in excess both aerobically and anaerobically. To increase the catabolic activity even further, experiments were carried out in the presence of 5 mM acetic acid or benzoic acid. However, there was almost no effect with acetate addition, whereas both respiratory (aerobically) and fermentative activities were elevated in the presence of benzoic acid. There was a strong negative correlation between glycolytic flux and intracellular ATP content; i.e., the higher the ATP content, the lower the rate of glycolysis. No correlation could be found with the other nucleotides tested (ADP, GTP, and UTP) or with the ATP/ADP ratio. Furthermore, a higher rate of glycolysis was not accompanied by an increasing level of glycolytic enzymes. On the contrary, the glycolytic enzymes decreased with increasing flux. The most pronounced reduction was obtained for HXK2 and ENO1. There was also a correlation between the extent of carbohydrate accumulation and glycolytic flux. A high accumulation was obtained at low glycolytic rates under glucose limitation, whereas nitrogen limitation during conditions of excess carbon and energy resulted in more or less complete depletion of intracellular storage carbohydrates irrespective of anaerobic or aerobic conditions. However, there was one difference in that glycogen dominated anaerobically whereas under aerobic conditions, trehalose was the major carbohydrate accumulated. Possible mechanisms which may explain the strong correlation between glycolytic flux, storage carbohydrate accumulation, and ATP concentrations are discussed.

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Year:  1997        PMID: 9393686      PMCID: PMC179672          DOI: 10.1128/jb.179.23.7243-7250.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  33 in total

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Review 4.  High-resolution NMR studies of Saccharomyces cerevisiae.

Authors:  S L Campbell-Burk; R G Shulman
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Journal:  Biochim Biophys Acta       Date:  1976-09-13

6.  Studies of anaerobic and aerobic glycolysis in Saccharomyces cerevisiae.

Authors:  J A den Hollander; K Ugurbil; T R Brown; M Bednar; C Redfield; R G Shulman
Journal:  Biochemistry       Date:  1986-01-14       Impact factor: 3.162

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Authors:  D Reibstein; J A den Hollander; S J Pilkis; R G Shulman
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Authors:  E Albers; C Larsson; G Lidén; C Niklasson; L Gustafsson
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9.  Glucose repression and hexokinase isoenzymes in yeast. Isolation and characterization of a modified hexokinase PII isoenzyme.

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10.  Reserve carbohydrate metabolism in Saccharomyces cerevisiae: responses to nutrient limitation.

Authors:  S H Lillie; J R Pringle
Journal:  J Bacteriol       Date:  1980-09       Impact factor: 3.490

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  40 in total

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6.  Quantitative Physiology of Non-Energy-Limited Retentostat Cultures of Saccharomyces cerevisiae at Near-Zero Specific Growth Rates.

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7.  Profiling of external metabolites during production of hantavirus nucleocapsid protein with recombinant Saccharomyces cerevisiae.

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8.  Effects of furfural on the respiratory metabolism of Saccharomyces cerevisiae in glucose-limited chemostats.

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Review 9.  Organization and regulation of the cytosolic NADH metabolism in the yeast Saccharomyces cerevisiae.

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10.  Effect of HXT1 and HXT7 hexose transporter overexpression on wild-type and lactic acid producing Saccharomyces cerevisiae cells.

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