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  • Nitrogen assimilation  (2)
  • Dichloroisoproterenol  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Planta 138 (1978), S. 123-125 
    ISSN: 1432-2048
    Schlagwort(e): Glutamate dehydrogenase ; Glutamine synthetase ; Glutamate synthetase ; Nitrogen assimilation ; Platymonas
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Platymonas striata Butcher displays significant levels of glutamate synthase (GS) (EC 2.6.1.53) and glutamine synthetase (GOGAT) (EC 6.3.1.2.), but very low levels of glutamate dehydrogenase (GDH) (EC 1.4.1.4). This suggests that the GS/GOGAT pathway is important for nitrogen assimilation. The in vitro rates of enzyme activity can however only account for about 10% of the in vivo rates of nitrogen assimilation. Nitrogen-starvation reduced GS activity to undetectable levels. On nitrate or ammonium ion refeeding the cellular GS activity was rapidly restored, and reached levels of 56% and 91% greater than the unstarved values 24h after refeeding nitrate or ammonium respectively.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1432-2048
    Schlagwort(e): Ammonium ion assimilation ; Nitrate assimilation ; Nitrogen assimilation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Studies on the mean cellular carbohydrate contents of Platymonas striata Butcher under conditions of nitrogen-starvation, and after refeeding these starved cultures with either nitrate or ammonium ions (growing under continuous illumination or with an alternating light/dark regime) have shown that nitrogen-starved cells accumulated abnormal amounts of cellular carbohydrate and that nitrogen refeeding produced a marked drop in the cellular carbohydrate. Cells grown in a light/dark regime accumulated less carbohydrates than those grown in continuous light. The mean cellular carbohydrate levels 16 h after nitrogen refeeding were still much in excess of those of cells grown with normal nutrition. It was therefore suggested that the differences in nitrogen uptakes in this period — when comparing either the uptake of cells grown in continuous light with that of cells grown in a light/dark regime; or when comparing the uptakes of cells presented with either nitrate or ammonium ions and grown in a light/dark regime —cannot be directly due to shortages of carbohydrate for the provision of carbon skeletons for nitrogen assimilation.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Protoplasma 115 (1983), S. 25-33 
    ISSN: 1615-6102
    Schlagwort(e): Dichloroisoproterenol ; Digestive vacuole ; Egestion ; Endocytosis ; Exocytosis ; Phagolysosome ; Tetrahymena ; Intracellular vacuolar movement
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Digestive vacuole formation inTetrahymena pyriformis GL-9 is inhibited by dichloroisoproterenol (dcipr). Inhibition is 95% at 150 μg/ml in starved cells, whereas the same level is achieved by 100 μg/ml in fed cells. The inhibition is rapid and easily reversed by washing the cells, which suggests that it is a surface effect. Dcipr at these concentrations has little, if any, lasting effect upon egestion, although in some cases there is a transient increase in rate for a short period after addition. Long-term starved (17–19 hours) and short-term starved (3 hours) cells, which had been allowed to form digestive vacuoles for varying periods of time, were then either treated with dcipr, or centrifuged to remove the cells from the suspension medium. These treatments stopped further formation of digestive vacuoles and produced cells with varying digestive vacuolar contents. Throughput times and rates of egestion were examined in the period after cessation of digestive vacuole formation and usually showed lengthening of the throughput times as the initial cellular digestive vacuolar content decreased, coupled with decreased rates of egestion. As far as has been ascertained these results cannot be explained by poorer nutrition due to lower cellular vacuolar contents. They accord with the idea that there is temporal sequencing of digestive vacuolar movement and egestion even when the cellular vacuolar content is low. It is thought that these alterations in throughput times and rates of egestion are largely the resultant of changes in rates of digestive vacuolar movement, rather than reductions in the capacity of the cytoproct to egest. Clearly the cell possesses some mechanism which links the rate of vacuolar movement (and possibly egestion) to cellular vacuolar content. Since cells with continuing vacuole formation show similar throughput times and rates of egestion to cells in which digestive vacuole formation has been stopped at high vacuolar content the linkage must be between vacuolar movement and cellular vacuolar content rather than with vacuole formation itself.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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