Physiological importance of quinoenzymes and the O-quinone family of cofactors

• Published in: The Journal of nutrition Vol. 130; no. 4; p. 719
• Main Authors: Stites, T E, Mitchell, A E, Rucker, R B
• Format: Journal Article
• Language: English
• Published: United States 01-04-2000
• Subjects: Animals; Coenzymes - metabolism; Dihydroxyphenylalanine - analogs & derivatives; Dihydroxyphenylalanine - chemistry; Dihydroxyphenylalanine - metabolism; Enzymes - metabolism; Humans; Indolequinones; Lysine - analogs & derivatives; Lysine - chemistry; Lysine - metabolism; PQQ Cofactor; Quinolones - chemistry; Quinolones - metabolism; Quinones - chemistry; Quinones - metabolism; Tryptophan - analogs & derivatives; Tryptophan - chemistry; Tryptophan - metabolism
• ISSN: 0022-3166
• DOI: 10.1093/jn/130.4.719

O-quinone cofactors derived from tyrosine and tryptophan are involved in novel biological reactions that range from oxidative deaminations to free-radical redox reactions. The formation of each of these cofactors appears to involve post-translational modifications of either tyrosine or tryptophan residues. The modifications result in cofactors, such as topaquinone (TPQ), tryptophan tryptophylquinone (TTQ), lysine tyrosylquinone (LTQ) or the copper-complexed cysteinyl-tyrosyl radical from metal-catalyzed reactions. Pyrroloquinoline quinone (PQQ) appears to be formed from the annulation of peptidyl glutamic acid and tyrosine residues stemming from their modification as components of a precursor peptide substrate. PQQ, a primary focus of this review, has invoked considerable interest because of its presence in foods, antioxidant properties and role as a growth-promoting factor. Although no enzymes in animals have been identified that exclusively utilize PQQ, oral supplementation of PQQ in nanomolar amounts increases the responsiveness of B- and T-cells to mitogens and improves neurologic function and reproductive outcome in rodents. Regarding TPQ and LTQ, a case may be made that the formation of TPQ and LTQ is also influenced by nutritional status, specifically dietary copper. For at least one of the amine oxidases, lysyl oxidase, enzymatic activity correlates directly with copper intake. TPQ and LTQ are generated following the incorporation of copper by a process that involves the two-step oxidation of a specified tyrosyl residue to first peptidyl dopa and then peptidyl topaquinone to generate active enzymes, generally classed as "quinoenzymes." Limited attention is also paid to TTQ and the copper-complexed cysteinyl-tyrosyl radical, cofactors important to fungal and bacterial redox processes.