Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Rate-limiting steps in metabolic pathways.

R Rognstad

    The Journal of Biological Chemistry
    |March 25, 1979
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a new method to identify rate-limiting enzymes in metabolic pathways. Using enzyme inhibitors, researchers found phosphoenolpyruvate carboxykinase is crucial for gluconeogenesis in fasted rat liver cells.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Glucose-6-phosphatase flux and the hepatic glucose balance model.

    The American journal of physiology·1996
    Same author

    Dicarboxylic acid fluxes during gluconeogenesis. No channelling of mitochondrial oxalacetate.

    Bulletin of mathematical biology·1995
    Same author

    Models of the liver pentose cycle.

    Journal of theoretical biology·1995
    Same author

    On the estimation of alternative pathways of fatty acid oxidation in the liver in vivo.

    Bulletin of mathematical biology·1995
    Same author

    Tests of the liver specificity of drug glucuronidation.

    Life sciences·1995
    Same author

    Isotopic estimation of the hepatic glucose balance in vivo.

    Journal of theoretical biology·1994
    Same journal

    Correction: Characterization of Mast2 kinase defines structural features, regulation, and substrates.

    The Journal of biological chemistry·2026
    Same journal

    Isotope-Edited ESEEM: A New Method for Probing Copper Binding Sites in Neurodegenerative Proteins.

    The Journal of biological chemistry·2026
    Same journal

    Introduction to the Thematic Review Series on Intracellular Protein Degradation. The ubiquitous biology of intracellular protein degradation: a tribute to Alfred L. ("Fred") Goldberg.

    The Journal of biological chemistry·2026
    Same journal

    Correction: Aromatic residue-rich amino-terminal segments of temporin L self-assemble into collagen-mimetic peptides with cell-adhesion properties.

    The Journal of biological chemistry·2026
    Same journal

    YhbO is a DJ-1 family glyoxalase and α-oxoaldehyde hydratase that confers resistance to reactive carbonyl stress (112).

    The Journal of biological chemistry·2026
    Same journal

    ARMH3 acts as a central scaffold at the Golgi/TGN through interactions with Arl5, GBF1, and PI4KB.

    The Journal of biological chemistry·2026
    See all related articles

    Area of Science:

    • Biochemistry
    • Metabolic Pathway Analysis
    • Enzyme Kinetics

    Background:

    • Identifying rate-limiting enzymes is crucial for understanding metabolic control.
    • Existing methods may not definitively distinguish rate-limiting steps.

    Purpose of the Study:

    • To propose and validate a novel method for detecting rate-limiting enzymes.
    • To investigate the role of phosphoenolpyruvate carboxykinase in gluconeogenesis.

    Main Methods:

    • Enzyme inhibition assays with varying inhibitor concentrations.
    • Observation of biphasic response curves to indicate enzyme non-rate-limiting status.
    • Application of the method to phosphoenolpyruvate carboxykinase in rat hepatocytes.

    Main Results:

    Related Experiment Videos

    • A biphasic response with an initial null effect reliably indicates a non-rate-limiting enzyme.
    • Phosphoenolpyruvate carboxykinase was identified as catalyzing a rate-limiting step.
    • This was observed in hepatocytes derived from fasted rats.

    Conclusions:

    • The proposed method offers a robust way to identify rate-limiting enzymes.
    • Phosphoenolpyruvate carboxykinase plays a critical role in lactate gluconeogenesis.
    • This finding has implications for understanding hepatic metabolic regulation.