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Home » Fate Of Pyruvate

Fate Of Pyruvate

July 28, 2025 by Kristensmith Taylor Leave a Comment

Fate Of Pyruvate

Question 1. Write four metabolic fates of pyruvic acid.
Answer:

The Fate of pyruvic acid:

1. In aerobic condition.

  • Pyruvic acid is converted to acetyl CoA in the presence of oxygen.
  • This acetyl CoA enters into the TCA cycle.

2. In gluconeogenesis.

  • Pyruvic acid is converted to glucose/glycogen.
  • This is used in gluconeogenesis.

“Understanding the fate of pyruvate through FAQs: Pathways, functions, and uses explained”

3. Transamination. 

  • Pyruvic acid is converted to alanine by transamination.

4. In anaerobic conditions.

  • Pyruvic acid is converted to lactic acid during anaerobic glycolysis by lactate dehydrogenase enzyme.

Question 2. Mention two inhibitors in the glycolytic pathway. How do they act?
Answer:

Carbohydrate glycolytic pathway

“Importance of studying the fate of pyruvate for medical students: Questions explained”

Question 3. Define gluconeogenesis. Mention the key enzymes of it.
Answer:

Definition:

  • The synthesis of glucose from non-carbohydrate compounds is known as gluconeogenesis.

Key enzymes:

  • Pyruvate carboxylase
  • Fructose 1, 6 – bisphosphate
  • Glucose 6 – phosphatase.

“Common challenges in mastering the fate of pyruvate notes effectively: FAQs provided”

Question 4. Significance of HMP pathway.
Answer:

  • The HMP pathway generates two important products.

1. Pentoses:

Used for the synthesis of nucleic acids and nucleotides.

2. NADPH:

  • Required for reductive biosynthesis of fatty acids and steroids.
  • Used in the synthesis of certain amino acids.
  • Brings about the detoxification of drugs.
  • Helps in phagocytosis.
  • Essential to preserve the integrity of the RBC membrane.

“Factors influencing success with the fate of pyruvate studies: Q&A”

Question 5. Various glycogen storage disorders.
Answer:

The metabolic defects concerned with glycogen synthesis and degradation are referred to as glycogen storage disorders. They occur due to enzyme defects.

Carbohydrate Various glycogen stroage disorders

“Steps to explain the pathways of pyruvate: Aerobic vs anaerobic metabolism: Q&A guide”

Question 6. Von Gierker’s disease
Answer: It is a metabolic defect concerned with the glycogen synthesis

Cause:

Glucose -6- phosphatase defect

“Role of pyruvate dehydrogenase in converting pyruvate to acetyl-CoA: Questions answered”

Clinical Features:

  • Enlarged liver and kidney
  • Fasting hypoglycemia
  • Lactic acidaemia
  • Hyperlipidaemia
  • Ketosis
  • Gouty arthritis

Filed Under: Anatomy

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