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Biosynthesis of coelenterazine in the deep-sea copepod, Metridia pacifica
Authors:Yuichi Oba  Shin-ichi Kato  Makoto Ojika
Institution:a Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya 464-860, Japan
b Yokohama Research Center, Chisso Co., 5-1 Okawa, Kanazawa-ku, Yokohama 236-8605, Japan
Abstract:Coelenterazine is an imidazopyrazinone compound (3,7-dihydroimidazopyrazin-3-one structure) that is widely distributed in marine organisms and used as a luciferin for various bioluminescence reactions. We have used electrospray ionization-ion trap-mass spectrometry to investigate whether the deep-sea luminous copepod Metridia pacifica is able to synthesize coelenterazine. By feeding experiments using deuterium labeled amino acids of l-tyrosine and l-phenylalanine, we have shown that coelenterazine can be synthesized from two molecules of l-tyrosine and one molecule of l-phenylalanine in M. pacifica. This is the first demonstration that coelenterazine is biosynthesized from free l-amino acids in a marine organism.
Keywords:RP-HPLC/ESI-IT-MS  reversed phase-high performance liquid chromatography equipped with electrospray ionization-ion trap-mass spectrometry  l-[D4]Tyr" target="_blank">l-[D4]Tyr  l-[2" target="_blank">deuterium labeled l-[2  3  5  6-D4]tyrosine  l-[D5]Phe" target="_blank">l-[D5]Phe  l-[2" target="_blank">l-[2  3  4  5  6-D5]phenylalanine
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