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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 117 (1978), S. 269-276 
    ISSN: 1432-072X
    Keywords: Succinic acid ; Fermentation ; Saccharomyces cerevisiae ; α-ketoglutarate dehydrogenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1. Succinic acid is formed in amounts of 0.2–1.7 g/l by fermenting yeasts of the genusSaccharomyces during the exponential growth phase. No differences were observed between the various species, respiratory deficient mutants and wild type strains. 2. At low glucose concentrations the formation of succinic acid depended on the amount of sugar fermented. However, the nitrogen source was found to be of greater importance than the carbon source. 3. Of all nitrogen sources, glutamate yielded the highest amounts of succinic acid. Glutamate led to an oxidative and aspartate to a reductive formation of succinic acid. 4. A reductive formation of succinic acid by the citric acid cycle enzymes was observed with malate. This was partially inhibited by malonate. No evidence was obtained that the glyoxylate cycle is involved in succinic acid formation by yeasts. 5. Anaerobically grown cells ofSaccharomyces cerevisiae contained α-ketoglutarate dehydrogenase. Its activity was found in the 175000 x g sediment after fractionated centrifugation. The specific activity increased 6-fold after growth on glutamate as compared with cells grown on ammonium sulfate. 6. The specific activities of malate dehydrogenase, fumarase, succinate dehydrogenase, succinylcoenzymeA synthetase, α-ketoglutarate dehydrogenase and glutamate dehydrogenase (nicotinamide adenine dinucleotide dependent) were determined in yeast cells grown on glutamate or ammonium sulfate. Similar results were obtained with a wild type strain and a respiratory deficient mutant. The latter did not contain succinate dehydrogenase. 7. In fermenting yeasts succinic acid is mainly formed from glutamate by oxidation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 358 (1997), S. 838-843 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A method for analysing arsenic in urine samples by Flow Injection Analysis-Atomic Absorption Spectrometry (FIA-AAS) after ultra-violet (UV) digestion is developed and validated. The validated method has the following performance characteristics: limit of detection (LOD) 0.5 μg L–1, repeatability and reproducibility better than 5% and 10% relative standard deviation (RSD) respectively for arsenic concentrations above 3 μg L–1, linear range 0.5–40 μg L–1. Validation of the method was performed by analysing several certified reference materials. Results obtained were well within the certified intervals. Several urine samples analysed by UV-FIA-AAS were also analysed by Inductively Coupled Plasma-Mass Spectrometry after High Performance Liquid Chromatography (HPLC-ICP-MS) in order to investigate comparability. Again results were satisfactory, arsenic concentrations in urine samples did not differ from each other significantly. Storage conditions were also studied. Urine samples are best stored in polyethylene containers at 5 ± 4°C and are stable in arsenic content for at least 30 days.
    Type of Medium: Electronic Resource
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