Copper Deficiency - Biochemical Etiology

Biochemical Etiology

Copper functions as a prosthetic group, which permits electron transfers in key enzymatic pathways like the electron transport chain. Copper is integrated in the enzymes cytochrome c oxidase, which is involved in cellular respiration and oxidative phosphorylation, Cu/Zn dismutase, which is involved in antioxidant defense, and many more listed in the table below.

Several Copper Dependent Enzymes and Their Function
Group Enzyme Function
Oxidases Flavin-containing amine oxidase Metabolism of neurotransmitters: noradrenaline, dopamine, serotonin and some dietary amines
Protein-lysine-6-oxidase (lysyl oxidase) Connective tissue synthesis- cross-linking of collagen and elastin
Copper-containing amine oxidase Metabolism of amines- histamines, putrescine, cadaverine
Cytochrome c oxidase Oxidative phosphorylation, electron transport in the mitochondrial membrane
Superoxide dismutase (Cu/Zn dismutase) Antioxidant and free radical scavenger, oxidizes dangerous superoxides to safer hydrogen peroxide
Ferroxidase I (ceruloplasmin) Iron transport-oxidation of Fe2+ to Fe 3+, copper storage and transport, antioxidant and free radical neutralizer
Hephaestin (ferroxidase) Iron transport and oxidation of Fe2+ to Fe3+ in intestinal cells to enable iron uptake
Monooxygenases Dopamine beta-monooxygenase Conversion of dopamine to norepinephrine
Peptidylglycine monooxygenase Peptide hormone maturation- amidation of alpha-terminal carboxylic acid group of glycine
Monophenol monooxygenase (Tyrosinase) Melanin synthesis
Methylation Cycle Methionine synthase Transfer of methyl group from methyltetrahydrofolate to homocysteine to generate methionine for the methylation cycle and tetrahydrofolate for purine synthesis
Adenosylhomocysteinase (S-Adenosyl-L-homocysteine) Regeneration of homocysteine from adenosylhomocyesteine (S-Adenosyl-L-homocysteine) in the methylation cycle

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