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Updated: Jun 25, 2026

Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET
Published on: October 9, 2021
Acid-induced change in ozone-reactive site in indole ring of tryptophan
Sueo Matsumura1, Ayuko Yoshimura, Kazuyuki Okazaki
1Department of Pathema Analysis, Kobe University Graduate School of Health Sciences, 7-10-2 Tomogaoka, Suma, Kobe 645-0142, Japan. matsmura@kobe-u.ac.jp
Abstract:
It is well established that ozone as well as oxygen activated by tryptophan 2,3-dioxygenase or indoleamine 2,3-dioxygenase cleave the 2,3-C=C bond of the indole ring of tryptophan to produce N-formylkynurenine. In the present study, however, we found that exposure of tryptophan to aqueous ozone at and below pH 4.5 generated a different compound. The compound was identified as kynurenine by high performance liquid chromatography and mass spectrometry. Exposure of N-formylkynurenine to acidic ozone did not generate a significant amount of kynurenine, indicating that the kynurenine was not produced via N-formylkynurenine. Acidic ozone thus appears to cleave the 1, 2-NAC bond in place of the 2,3-C=C bond of the indole ring, followed by liberation of the 2-C atom. The 1,2-NAC bond and 2,3-C=C bond are likely to undergo changes in their nature of bonding on acidification, enabling ozone to react with the former bond but not with the latter bond.
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