Biochemistry: Glycolysis and Cellular Respiration
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Questions and Answers

What is the name of the genetic disorder caused by the deficiency of enzyme HGPRT?

  • Lesch-Nyhan syndrome (correct)
  • A-SCID
  • Cystic fibrosis
  • Down syndrome
  • Which enzyme is deficient in Type I Crigler-Najjar Syndrome?

  • UDP glucuronosyl transferase (correct)
  • delta-aminolevulinic acid synthase I
  • Uroporphyrinogen synthase III
  • Ferrochelatase
  • Which of the following enzymes of the heme synthesis pathway is found in the cytosol?

  • Uroporphyrinogen synthase III
  • Ferrochelatase
  • Protoporphyrinogen oxidase
  • delta-aminolevulinic acid synthase I (correct)
  • Which lipoprotein transports triglycerides from the intestine to peripheral tissues?

    <p>Chylomicron</p> Signup and view all the answers

    Which of the following is not involved in the production of Creatine?

    <p>Alanin</p> Signup and view all the answers

    What is the process of generating glucose from non-carbohydrate precursors called?

    <p>Gluconeogenesis</p> Signup and view all the answers

    Which of the following is a genetic disorder caused by a mutation of the gene that encodes for LDL receptor?

    <p>Familial Hypercholesterolemia</p> Signup and view all the answers

    What is the byproduct of guanine degradation in the body?

    <p>Uric acid</p> Signup and view all the answers

    Which enzyme is responsible for converting glycine to creatine?

    <p>Glycine amidinotransferase</p> Signup and view all the answers

    Which of the following lipoproteins is involved in the transport of cholesterol from the liver to peripheral tissues?

    <p>LDL</p> Signup and view all the answers

    Study Notes

    Glycolysis and Gluconeogenesis

    • During lactate formation, NAD is reconverted into NADH.
    • Pyruvate kinase deficiency leads to hemolytic anemia.
    • Arsenate poisoning inhibits the step involving 3-phosphoglycerate mutase, Enolase, Pyruvate kinase, or Glyceraldehyde-3-phosphate dehydrogenase.
    • The Cori Cycle involves the transport of lactate from skeletal muscle to the liver for gluconeogenesis.
    • The net gain of ATP during the conversion of glucose to pyruvate is 2 ATP.
    • Glucagon is the hormone responsible for increasing gluconeogenesis in the liver during prolonged starvation.
    • Lactate dehydrogenase catalyzes the conversion of pyruvate to lactate.
    • Acetyl CoA is not a substrate for gluconeogenesis.

    Enzymes and Reactions

    • The conversion of glucose to pyruvate generates 2 NADH molecules.
    • The conversion of glyceraldehydes-3-phosphate to 1-3-bisphosphoglycerate generates NADH.
    • Lipoprotein lipase is present in the endothelial surfaces of adipose tissues in the heart and is required for hydrolysis and release of triglycerides from chylomicrons.
    • Apolipoprotein present in chylomicron serves as the activator of lipoprotein lipase.

    Biochemistry and Pathology

    • Glucose oxidase catalyzes the oxidation of glucose to gluconic acid and hydrogen peroxide (H202).
    • Elevated cholesterol levels may occur with hypothyroidism.
    • Creatinine is an interfering factor of glucose measurement.
    • High levels of ascorbic acid do not interfere with chromogen for H2O2 in glucose assay.
    • Clofibrate increases serum TG level.
    • DiacetylMonoxime (DAM) is a chemical method of serum urea measurement.
    • Hypocalcemia increases serum phosphate level.

    Bilirubin and Cholesterol

    • Bilirubin is the product of globin.
    • Total bilirubin is direct bilirubin + indirect bilirubin.
    • Indirect bilirubin is unconjugated bilirubin.
    • Bilirubin is measured by the diazo method.
    • The acceptable range of serum cholesterol level is 200 mg/dl.

    Genetic Disorders

    • Lesch-Nyhan syndrome is caused by the deficiency of enzyme HGPRT.
    • UDP glucuronosyl transferase is the enzyme deficient in Type I Crigler-Najjar Syndrome.
    • delta-aminolevulinic acid synthase I is an enzyme found in the cytosol of the heme synthesis pathway.
    • Familial Hypercholesterolemia is a codominant genetic disorder caused by a mutation of the gene that encodes for LDL receptor.
    • Chylomicron is the lipoprotein that transports triglycerides from the intestine to peripheral tissues.
    • Glycine, Arginine, and S-adenosyl methionine are involved in the production of Creatine.
    • Gluconeogenesis is the process of generating glucose from non-carbohydrate precursors.

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    Description

    This quiz tests your understanding of glycolysis, cellular respiration, and related enzyme deficiencies. It covers topics such as NADH, lactate formation, and the effects of arsenate poisoning.

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