Difficulty: Easy
Correct Answer: Amino acid converted to a keto acid plus ammonia
Explanation:
Introduction / Context:
Oxidative deamination removes an amino group from an amino acid while oxidizing the carbon skeleton, typically generating a corresponding alpha-keto acid and free ammonia. This reaction is central to hepatic nitrogen disposal and integration with the tricarboxylic acid cycle via alpha-ketoglutarate and other intermediates.
Given Data / Assumptions:
Concept / Approach:
Differentiate oxidative deamination from transamination. Transamination transfers amino groups between amino acids and alpha-keto acids without releasing ammonia. Oxidative deamination releases ammonia and produces a keto acid from the original amino acid carbon skeleton.
Step-by-Step Solution:
Verification / Alternative check:
Enzymatic assays for glutamate dehydrogenase demonstrate stoichiometric production of NH3 and alpha-keto acids, confirming the definition.
Why Other Options Are Wrong:
Option A describes transamination, not oxidative deamination. Options B and E propose products (carboxylic acid or aldehyde) that are not standard outcomes. Option D misconstrues the chemistry.
Common Pitfalls:
Mixing up “transfer” (transamination) with “release” (oxidative deamination) of ammonia.
Final Answer:
Amino acid converted to a keto acid plus ammonia
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