Factors relevant in the reaction of pyroloquinoline quinone with amino acids
Open Access
- 1 July 1989
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 183 (1), 41-47
- https://doi.org/10.1111/j.1432-1033.1989.tb14894.x
Abstract
In order to reveal the stability of pyrroloquinoline quinone (PQQ) in complex samples, its reaction on incubation with amino acids was followed spectrophotometrically by monitoring oxygen consumption, and with a biological assay. For several α-amino acids, the formation of a yellow coloured compound (λmax= 420 nm) was accompanied by oxygen uptake and disappearnace of biological activity from the reaction mixture. The yellow product appeared to be an oxazole of PQQ, the exact structure depending on the amino acid used. Oxazole formation also occurred under anaerobic conditions with concomitant formation of PQQH2, suggesting that PQQ is able to oxidize the presumed oxazoline to the oxazole. Besides the condensation reaction, there is also a catalytic cycle in which an aldimine adduct of PQQ and the amino acid is converted into the aminophenol form of the cofactor and an aldehyde resulting from oxidative decarboxylation of the amino acid. Addition of NH4+ salts, as well as that of certain divalent cations, greatly stimulated both the cyclic and the linear reaction. With basic amino acids, oxazole formation scarcely occurred. However, as oxygen consumption was observed (provided that certain divalent cations were present), conversion of these compounds took place. A reaction scheme is proposed accounting for the products formed and the effects observed. Since NH4+ ions activate several quinoproteins (PQQ-containing enzymes) and divalent cations (Ca2+, Fe2+, and Cu2+) are additional (co)factors in certain metallo quinoproteins, the effects of metal ions observed here could be related to the mechanistic features of these enzymes. Although all oxazoles were converted to PQQ by acid hydrolysis, PQQ was not detected when hydrolysis was carried out in the presence of tryptophan, a compound which appeared to have a deleterious effect on the cofactor under this condition. The results here described explain why analysis methods for free PQQ in complex samples fail in certain cases, or are not quantitative.Keywords
This publication has 25 references indexed in Scilit:
- Evidence for PQQ as cofactor in 3,4‐dihydroxyphenylalanine (dopa) decarboxylase of pig kidneyFEBS Letters, 1988
- L‐tyrosine is the precursor of PQQ biosynthesis in Hyphomicrobium XFEBS Letters, 1988
- Pyrroloquinoline quinone (PQQ) is the organic cofactor in soybean lipoxygenase‐1FEBS Letters, 1988
- The interaction of aminogroups with pyrroloquinoline quinone as detected by the reduction of nitroblue tetrazoliumBiochemical and Biophysical Research Communications, 1988
- Phenylhydrazine as probe for cofactor identification in amine oxidoreductases Evidence for PQQ as the cofactor in methylamine dehydrogenaseFEBS Letters, 1987
- Kinetic Studies on the Oxidation of Thiols by Coenzyme PQQBulletin of the Chemical Society of Japan, 1987
- PQQ and quinoprotein enzymes in microbial oxidationsFEMS Microbiology Letters, 1986
- Mode of binding of pyrroloquinoline quinone to apo-glucose dehydrogenase.Agricultural and Biological Chemistry, 1985
- Evidence of a quinoprotein glucose dehydrogenase apoenzyme in several strains of Escherichia coliFEMS Microbiology Letters, 1984
- Bovine serum amine oxidase: a mammalian enzyme having covalently bound PQQ as prosthetic groupFEBS Letters, 1984