[Comparative studies of the glycolytic enzymes of Dicrocoelium dendriticum (Trematoda) and rat liver].

@article{Khler1972ComparativeSO,
  title={[Comparative studies of the glycolytic enzymes of Dicrocoelium dendriticum (Trematoda) and rat liver].},
  author={Piotr K{\"o}hler},
  journal={Zeitschrift fur Parasitenkunde},
  year={1972},
  volume={38 1},
  pages={
          54-65
        }
}
  • P. Köhler
  • Published 1972
  • Biology
  • Zeitschrift fur Parasitenkunde
6 Citations
Glucose and pyruvate catabolism in Litomosoides carinii
TLDR
Isotopic carbon balance studies and experiments in which substrates specifically labelled with 14 C were employed showed that substrate carbon can to some extent enter into respiratory CO 2 , and it is suggested that complete oxidation of carbon substrate may be of relevance as an energy-conserving pathway in the filarial worm.
Metabolic role of pyruvate kinase in the trematode Dicrocoelium dendriticum.
  • P. Köhler
  • Biology
    Comparative biochemistry and physiology. B, Comparative biochemistry
  • 1974
Intermediary metabolism in Dicrocoelium dendriticum (Trematoda).
[Oxygen consumption, substrate absorption and lactate excretion of Dicrocoelium dendriticum (Trematoda)].
Adulte Dicrocoelium dendriticum enthielten 8,6 mg Protein, 7,5 mg Kohlenhydrate (davon 5,7 mg Glykogen), 2,9 mg Lipide und 1,2 mg Asche pro 100 mg Frischgewicht. Die Atmung der intakten Parasiten

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ENZYME PATTERNS IN HUMAN TISSUES. I. METHODS FOR THE DETERMINATION OF GLYCOLYTIC ENZYMES.
TLDR
Improved methods and a unified program for the determination of all the glycolytic and some related enzymes in crude tissue homogenates have been described, and the precision of the measurements and the stability of the enzymes to storage in the intact tissues at -20°C have been established.
Diphosphofructose-Aldolase, Phosphoglyceraldehyd-Dehydrogenase, Milchsäure-Dehydrogenase, Glycerophosphat-Dehydrogenase und Pyruvat-Kinase aus Kaninchenmuskulatur in einem Arbeitsgang
Extrakt von Kaninchenmuskulatur wird durch steigende Sättigung mit Ammonsulfat in amorphe Fraktionen aufgeteilt, aus denen sich ohne weitere Reinigungsschritte die obengenannten Fermente