» Articles » PMID: 31462497

Bioluminescence Chemistry of Fireworm

Abstract

Marine polychaetes , commonly known as fireworms, emit bright blue-green bioluminescence. Until the recent identification of the luciferase enzyme, little progress had been made toward characterizing the key components of this bioluminescence system. Here we present the biomolecular mechanisms of enzymatic (leading to light emission) and nonenzymatic (dark) oxidation pathways of newly described luciferin. Spectral studies, including 1D and 2D NMR spectroscopy, mass spectrometry, and X-ray diffraction, of isolated substances allowed us to characterize the luciferin as an unusual tricyclic sulfur-containing heterocycle. luciferin does not share structural similarity with any other known luciferins. The structures of the bioluminescent system's low molecular weight components have enabled us to propose chemical transformation pathways for the enzymatic and nonspecific oxidation of luciferin.

Citing Articles

Maintain the light, long-term seasonal monitoring of luminous capabilities in the brittle star Amphiura filiformis.

Coubris C, Duchatelet L, Delroisse J, Bayaert W, Parise L, Eloy M Sci Rep. 2024; 14(1):13238.

PMID: 38853171 PMC: 11163003. DOI: 10.1038/s41598-024-64010-x.


Cryo-EM structure of the fatty acid reductase LuxC-LuxE complex provides insights into bacterial bioluminescence.

Tian Q, Wu J, Xu H, Hu Z, Huo Y, Wang L J Biol Chem. 2022; 298(6):102006.

PMID: 35504354 PMC: 9157457. DOI: 10.1016/j.jbc.2022.102006.


Violet bioluminescent Polycirrus sp. (Annelida: Terebelliformia) discovered in the shallow coastal waters of the Noto Peninsula in Japan.

Kanie S, Miura D, Jimi N, Hayashi T, Nakamura K, Sakata M Sci Rep. 2021; 11(1):19097.

PMID: 34580316 PMC: 8476577. DOI: 10.1038/s41598-021-98105-6.


Seeing (and Using) the Light: Recent Developments in Bioluminescence Technology.

Love A, Prescher J Cell Chem Biol. 2020; 27(8):904-920.

PMID: 32795417 PMC: 7472846. DOI: 10.1016/j.chembiol.2020.07.022.


Palette of Luciferases: Natural Biotools for New Applications in Biomedicine.

Kotlobay A, Kaskova Z, Yampolsky I Acta Naturae. 2020; 12(2):15-27.

PMID: 32742724 PMC: 7385095. DOI: 10.32607/actanaturae.10967.


References
1.
Land E, Riley P . Spontaneous redox reactions of dopaquinone and the balance between the eumelanic and phaeomelanic pathways. Pigment Cell Res. 2000; 13(4):273-7. DOI: 10.1034/j.1600-0749.2000.130409.x. View

2.
Shimomura O, Beers J, Johnson F . THE CYANIDE ACTIVATION OF ODONTOSYLLIS LUMINESCENCE. J Cell Comp Physiol. 1964; 64:15-21. DOI: 10.1002/jcp.1030640103. View

3.
Dubinnyi M, Kaskova Z, Rodionova N, Baranov M, Gorokhovatsky A, Kotlobay A . Novel mechanism of bioluminescence: oxidative decarboxylation of a moiety adjacent to the light emitter of Fridericia luciferin. Angew Chem Int Ed Engl. 2015; 54(24):7065-7. DOI: 10.1002/anie.201501668. View

4.
Branchini B, Behney C, Southworth T, Fontaine D, Gulick A, Vinyard D . Experimental Support for a Single Electron-Transfer Oxidation Mechanism in Firefly Bioluminescence. J Am Chem Soc. 2015; 137(24):7592-5. DOI: 10.1021/jacs.5b03820. View

5.
Lopalco A, Dalwadi G, Niu S, Schowen R, Douglas J, Stella V . Mechanism of Decarboxylation of Pyruvic Acid in the Presence of Hydrogen Peroxide. J Pharm Sci. 2015; 105(2):705-713. PMC: 4814373. DOI: 10.1002/jps.24653. View