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Enzymatic conversion of dehydrocoelenterazine to coelenterazine using FMN-bound flavin reductase of NAD(P)H:FMN oxidoreductase.
Inouye, Satoshi; Nakamura, Mitsuhiro; Hosoya, Takamitsu.
Afiliación
  • Inouye S; Yokohama Research Center, JNC Co., 5-1 Okawa, Kanazawa-ku, Yokohama, 236-8605, Japan. Electronic address: sinouye@jnc-corp.co.jp.
  • Nakamura M; Graduate School of Technology, Industrial and Social Sciences, Tokushima University, Tokushima, 770-8506, Japan.
  • Hosoya T; Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo, 101-0062, Japan.
Biochem Biophys Res Commun ; 587: 24-28, 2022 01 08.
Article en En | MEDLINE | ID: mdl-34864391
Coelenterazine (CTZ) is known as luciferin (a substrate) for the luminescence reaction with luciferase (an enzyme) in marine organisms and is unstable in aqueous solutions. The dehydrogenated form of CTZ (dehydrocoelenterazine, dCTZ) is stable and thought to be a storage form of CTZ and a recycling intermediate from the condensation reaction of coelenteramine and 4-hydroxyphenylpyruvic acid to CTZ. In this study, the enzymatic conversion of dCTZ to CTZ was successfully achieved using NAD(P)H:FMN oxidoreductase from the bioluminescent bacterium Vibrio fischeri ATCC 7744 (FRase) in the presence of NADH (the FRase-NADH reaction). CTZ reduced from dCTZ in the FRase-NADH reaction was identified by HPLC and LC/ESI-TOF-MS analyses. Thus, dCTZ can be enzymatically converted to CTZ in vitro. Furthermore, the concentration of dCTZ could be determined by the luminescence activity using the CTZ-utilizing luciferases (Gaussia luciferase or Renilla luciferase) coupled with the FRase-NADH reaction.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pirazinas / Proteínas Bacterianas / Renilla / Aliivibrio fischeri / Imidazoles / Luciferasas / NADH NADPH Oxidorreductasas Límite: Animals Idioma: En Revista: Biochem Biophys Res Commun Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pirazinas / Proteínas Bacterianas / Renilla / Aliivibrio fischeri / Imidazoles / Luciferasas / NADH NADPH Oxidorreductasas Límite: Animals Idioma: En Revista: Biochem Biophys Res Commun Año: 2022 Tipo del documento: Article