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Amino Acid Metabolism problems


  • 1. A person with phenylketonuria is advised not to consume which of the following products?

  • Options
  • A. Glycine containing foods
  • B. Fat containing food
  • C. Glucose
  • D. Aspartame
  • Discuss
  • 2. A ketogenic amino acid is one which degrades to

  • Options
  • A. keto-sugars
  • B. either acetyl CoA or acetoacetyl CoA
  • C. pyruvate or citric acid cycle intermediates
  • D. multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA
  • Discuss
  • 3. An example of a transamination process is

  • Options
  • A. glutamate = hexanoic acid + NH3
  • B. aspartate + hexanoic acid = glutamate + oxaloacetate
  • C. aspartate + ? ketoglutarate = glutamate + oxaloacetate
  • D. glutamate = ?-ketoglutarate + NH3
  • Discuss
  • 4. Histidine is degraded to ?-ketoglutarate and is described as a

  • Options
  • A. gluco amino acid
  • B. glucogenic amino acid
  • C. ketogenic amino acid
  • D. keto-gluco amino acid
  • Discuss
  • 5. Which of the following is the best described glucogenic amino acid?

  • Options
  • A. Lysine
  • B. Tryptophan
  • C. Valine
  • D. None of these
  • Discuss
  • 6. A glucogenic amino acid is one which is degraded to

  • Options
  • A. keto-sugars
  • B. either acetyl CoA or acetoacetyl CoA
  • C. pyruvate or citric acid cycle intermediates
  • D. none of the above
  • Discuss
  • 7. A best described ketogenic amino acid is

  • Options
  • A. lysine
  • B. tryptophan
  • C. valine
  • D. none of these
  • Discuss
  • 8. Transamination is the transfer of an amino

  • Options
  • A. acid to a carboxylic acid plus ammonia
  • B. group from an amino acid to a keto acid
  • C. acid to a keto acid plus ammonia
  • D. group from an amino acid to a carboxylic acid
  • Discuss
  • 9. A person with phenylketonuria will convert

  • Options
  • A. phenylalanine to phenylpyruvate
  • B. phenylalanine to isoleucine
  • C. phenylpyruvate to phenylalanine
  • D. tyrosine to phenylalanine
  • Discuss
  • 10. A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of

  • Options
  • A. phenylalanine
  • B. phenylpyruvate
  • C. tyrosine
  • D. isoleucine
  • Discuss

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