Elucidating the Light-Emitting Species Generated from Aminoluciferin in Firefly/Beetle Bioluminescence

Oxyluciferin is the key photon emitter in the firefly/beetle luciferase-catalyzed bioluminescence reaction, and elucidating its chemical form within the active site of luciferase is essential for understanding and modulating emission wavelength. In this study, we focused on aminoluciferin (AL), a d-luciferin (d-LH<sub>2</sub>) analog in which the hydroxy group is substituted with an amino group. AL has been widely used as an alternative substrate to d-LH<sub>2</sub> and in the development of bioluminescence probes. To identify the emissive form of AL in bioluminescence, we synthesized OxyAL (the emitter derived from AL) and 5-methyl-OxyAL, and measured their fluorescence spectra under various conditions. We assigned the range of emission wavelengths of keto-, enol- and enolate-OxyAL using 5,5-dimethyl-OxyAL, fixed in the keto form, as a reference. Based on spectral assignments and comparison with the bioluminescence spectra of AL, we conclude that enolate-OxyAL is the most probable light-emitting species in the active site of luciferase. These findings provide new insight into AL-based bioluminescence.

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Publication Details

Journal
Chemical and Pharmaceutical Bulletin
Published
2025-08-08
DOI
https://doi.org/10.1248/cpb.c25-00302
Primary Topic
bioluminescence and chemiluminescence research
Type
article
Field-Weighted Citation Impact
0.00

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article

Elucidating the Light-Emitting Species Generated from Aminoluciferin in Firefly/Beetle Bioluminescence

Yasuteru Urano, Takeaki Ozawa, Ryosuke Kojima, Hideo Takakura
Chemical and Pharmaceutical Bulletin
bioluminescence and chemiluminescence research
article

Elucidating the Light-Emitting Species Generated from Aminoluciferin in Firefly/Beetle Bioluminescence

Yasuteru Urano, Takeaki Ozawa, Ryosuke Kojima, Hideo Takakura
article en

Abstract

Oxyluciferin is the key photon emitter in the firefly/beetle luciferase-catalyzed bioluminescence reaction, and elucidating its chemical form within the active site of luciferase is essential for understanding and modulating emission wavelength. In this study, we focused on aminoluciferin (AL), a d-luciferin (d-LH<sub>2</sub>) analog in which the hydroxy group is substituted with an amino group. AL has been widely used as an alternative substrate to d-LH<sub>2</sub> and in the development of bioluminescence probes. To identify the emissive form of AL in bioluminescence, we synthesized OxyAL (the emitter derived from AL) and 5-methyl-OxyAL, and measured their fluorescence spectra under various conditions. We assigned the range of emission wavelengths of keto-, enol- and enolate-OxyAL using 5,5-dimethyl-OxyAL, fixed in the keto form, as a reference. Based on spectral assignments and comparison with the bioluminescence spectra of AL, we conclude that enolate-OxyAL is the most probable light-emitting species in the active site of luciferase. These findings provide new insight into AL-based bioluminescence.

Chemical and Pharmaceutical BulletinVol. 73(8)
Kansai Medical University (JP), The University of Tokyo (JP)
Japan Society for the Promotion of Science
Life in Land
Openalex Percentile: Top 82%
bioluminescence and chemiluminescence research
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