A practical, biomimetic, one-pot synthesis of firefly luciferin

The bioluminescence reaction of firefly luciferase with D-luciferin has become an indispensable imaging technique in modern biology and life science experiments, but the high cost of D-luciferin is limiting its further application. Here, we report a practical, one-pot synthesis of D-luciferin from p-benzoquinone (p-BQ), L-cysteine methyl ester and D-cysteine, with an overall yield of 46%. Our route, which is six steps in length and proceeds via 2-cyano-6-hydroxybenzothiazole, is inspired by the mechanistic study of our previously reported biomimetic, non-enzymatic, one-pot formation of L-luciferin from p-BQ and L-cysteine. Advantages of our route include its high yield, low cost, use of only inexpensive, commercially available reagents, without requiring strictly anhydrous and oxygen-free conditions, and elevated temperatures.

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Publication Details

Journal
Scientific Reports
Published
2024-12-25
DOI
https://doi.org/10.1038/s41598-024-82996-2
Citations
4
Primary Topic
bioluminescence and chemiluminescence research
Type
article
Field-Weighted Citation Impact
0.94

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article

A practical, biomimetic, one-pot synthesis of firefly luciferin

Yuichi Oba, Toshio Nishikawa, Shusei Kanie, Mituo Kato et al.
4 citations
Scientific Reports
bioluminescence and chemiluminescence research
0.94
article

A practical, biomimetic, one-pot synthesis of firefly luciferin

Yuichi Oba, Toshio Nishikawa, Shusei Kanie, Mituo Kato, K. Tsuchihashi
article en
4 citations

Abstract

The bioluminescence reaction of firefly luciferase with D-luciferin has become an indispensable imaging technique in modern biology and life science experiments, but the high cost of D-luciferin is limiting its further application. Here, we report a practical, one-pot synthesis of D-luciferin from p-benzoquinone (p-BQ), L-cysteine methyl ester and D-cysteine, with an overall yield of 46%. Our route, which is six steps in length and proceeds via 2-cyano-6-hydroxybenzothiazole, is inspired by the mechanistic study of our previously reported biomimetic, non-enzymatic, one-pot formation of L-luciferin from p-BQ and L-cysteine. Advantages of our route include its high yield, low cost, use of only inexpensive, commercially available reagents, without requiring strictly anhydrous and oxygen-free conditions, and elevated temperatures.

Scientific ReportsVol. 14(1)
Chubu University (JP), Nagoya University (JP), National Institute of Advanced Industrial Science and Technology (JP)
Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Openalex Percentile: Top 24%
bioluminescence and chemiluminescence research
0.94
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