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一种实用的、仿生的、一锅法合成萤火虫荧光素。

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

作者信息

Kato Maria, Tsuchihashi Kazuaki, Kanie Shusei, Oba Yuichi, Nishikawa Toshio

机构信息

Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan.

Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Hokkaido Center, Sapporo, 062-8517, Japan.

出版信息

Sci Rep. 2024 Dec 25;14(1):30461. doi: 10.1038/s41598-024-82996-2.

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.

摘要

萤火虫荧光素酶与D - 荧光素的生物发光反应已成为现代生物学和生命科学实验中不可或缺的成像技术,但D - 荧光素的高成本限制了其进一步应用。在此,我们报道了一种从对苯醌(p - BQ)、L - 半胱氨酸甲酯和D - 半胱氨酸出发,实用的一锅法合成D - 荧光素的方法,总产率为46%。我们的路线长度为六步,通过2 - 氰基 - 6 - 羟基苯并噻唑进行,其灵感来自于我们之前报道的由p - BQ和L - 半胱氨酸仿生、非酶一锅法形成L - 荧光素的机理研究。我们路线的优点包括高产率、低成本、仅使用廉价的市售试剂、无需严格的无水无氧条件以及高温。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a5/11669719/2d0d435394cf/41598_2024_82996_Fig1_HTML.jpg

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