Q.32 Match the entries inGroup I with the enzymes inGroup II. Group I                                                      Group II P. NAD+                                            1. Glutathione peroxidase Q. Selenium                                      2. Nitrogenase R. Pyridoxal phosphate                  3. Lactate dehydrogenase S. Molybdenum                               4. Glycogen phosphorylase (A) P-3, Q-2, R-4, S-1 (B) P-4, Q-1, R-3, S-2 (C) P-3, Q-1, R-4, S-2 (D) P-3, Q-4, R-2, S-1

Q.32 Match the entries inGroup I with the enzymes inGroup II.
Group I                                                      Group II
P. NAD+                                            1. Glutathione peroxidase
Q. Selenium                                      2. Nitrogenase
R. Pyridoxal phosphate                  3. Lactate dehydrogenase
S. Molybdenum                               4. Glycogen phosphorylase
(A) P-3, Q-2, R-4, S-1 (B) P-4, Q-1, R-3, S-2
(C) P-3, Q-1, R-4, S-2 (D) P-3, Q-4, R-2, S-1

Enzyme Cofactor Matching: NAD+, Selenium, PLP, Molybdenum

Correct Answer: (C) P-3, Q-1, R-4, S-2. NAD+ serves lactate dehydrogenase, selenium enables glutathione peroxidase, pyridoxal phosphate activates glycogen phosphorylase, and molybdenum powers nitrogenase.

Cofactor-Enzyme Roles

Metalloenzymes and vitamin-derived cofactors catalyze essential reactions in metabolism and redox homeostasis. Trace elements like selenium integrate as selenocysteine, while organic cofactors like NAD+ transfer hydride equivalents in dehydrogenases.

Correct Matching Breakdown

P. NAD+ → 3. Lactate dehydrogenase. NAD+ accepts hydride from lactate, forming NADH in anaerobic glycolysis; LDH catalyzes L-lactate + NAD+ ⇌ pyruvate + NADH + H+.

Q. Selenium → 1. Glutathione peroxidase. Selenocysteine (Sec) at the active site reduces H₂O₂ and lipid hydroperoxides: 2GSH + H₂O₂ → GSSG + 2H₂O, preventing oxidative damage.

R. Pyridoxal phosphate → 4. Glycogen phosphorylase. PLP forms a Schiff base with lysine, orienting glycogen for phosphorolytic cleavage: (glycogen)n + Pi → (glycogen){n-1} + glucose-1-P.

S. Molybdenum → 2. Nitrogenase. MoFe-protein contains molybdenum in the FeMoco cluster, catalyzing N₂ + 8H+ + 8e- + 16ATP → 2NH₃ + H₂ + 16ADP + 16Pi.

Option Analysis

Option (A) P-3, Q-2, R-4, S-1 incorrectly pairs selenium with nitrogenase (Mo-specific) and molybdenum with GPx (selenoprotein).

Option (B) P-4, Q-1, R-3, S-2 mismatches NAD+ to glycogen phosphorylase (PLP-dependent) and PLP to LDH (NAD+ hydride transfer).

Option (D) P-3, Q-4, R-2, S-1 wrongly assigns selenium to phosphorylase (PLP cofactor) and molybdenum to GPx (selenium-requiring).

Biochemical Relevance

These pairings highlight micronutrient deficiencies’ metabolic impacts—selenium depletion cripples antioxidant defense, molybdenum limits nitrogen fixation, PLP shortages impair glycogenolysis, and NAD+ deficits disrupt fermentation.

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