Trace minerals — Which mineral primarily supports protein metabolism and functions as a cofactor in oxidation–reduction (redox) reactions within antioxidant enzymes?

Difficulty: Medium

Correct Answer: Manganese

Explanation:


Introduction / Context:
Several trace minerals act as enzyme cofactors in metabolism. One mineral is notable for roles in amino acid and protein metabolism, bone formation, and as a catalytic component of key redox enzymes, including a mitochondrial form of superoxide dismutase. This question asks you to identify that mineral.


Given Data / Assumptions:

  • Protein metabolism involves urea cycle and amino acid–modifying enzymes.
  • Antioxidant defense relies on superoxide dismutases and other redox enzymes.
  • Trace minerals can be enzyme-bound at active sites.


Concept / Approach:
Manganese serves as a cofactor for multiple enzymes: Mn-superoxide dismutase (MnSOD) in mitochondria (redox defense), arginase (urea cycle; protein nitrogen handling), and pyruvate carboxylase, among others. While molybdenum is also a redox cofactor (xanthine oxidase, sulfite oxidase), it is less associated with protein metabolism per se. Magnesium broadly stabilizes ATP and nucleotides but is not specifically a protein-metabolism/redox cofactor in the same way, and calcium is chiefly signaling/structural.


Step-by-Step Solution:

List candidate roles: antioxidant enzyme (MnSOD) + protein/urea-cycle enzyme (arginase) → points to manganese.Contrast with molybdenum: oxidases of purines/sulfite, less tied to protein pathways.Eliminate nonspecific ions: magnesium (ATP binding) and calcium (signaling) do not match both clues.Select manganese as best fitting both protein metabolism and redox actions.


Verification / Alternative check:
Biochemical assays localize MnSOD to the mitochondrial matrix; genetic loss or dietary deficiency impairs oxidative stress handling and can alter nitrogen metabolism, consistent with manganese’s dual functional profile.


Why Other Options Are Wrong:

  • Molybdenum: important in oxidases but not primarily in protein metabolism.
  • Magnesium: ubiquitous ATP cofactor, not a targeted redox/protein metabolism match.
  • Calcium: signal transduction and bone mineral; not an oxidation–reduction enzyme cofactor.
  • Zinc: many enzymes (including in protein metabolism), but the redox enzyme hallmark specified here (MnSOD) contains manganese, not zinc.


Common Pitfalls:
Equating “redox cofactor” only with molybdenum or iron. The mitochondrial SOD specifically uses manganese, a distinctive clue embedded in the question.


Final Answer:
Manganese.

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