Biochemistry: Glycolysis and Cellular Respiration
10 Questions
0 Views

Choose a study mode

Play Quiz
Study Flashcards
Spaced Repetition
Chat to lesson

Podcast

Play an AI-generated podcast conversation about this lesson

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.

    Studying That Suits You

    Use AI to generate personalized quizzes and flashcards to suit your learning preferences.

    Quiz Team

    Related Documents

    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.

    More Like This

    Glycolysis Overview
    19 questions

    Glycolysis Overview

    CharitableGoshenite9955 avatar
    CharitableGoshenite9955
    Glycolysis ATP Payoff Phase
    10 questions
    Use Quizgecko on...
    Browser
    Browser