Yokohama Research Center, JNC Co., 5-1 Okawa, Kanazawa-ku, Yokohama, 236-8605, Japan.
Graduate School of Technology, Industrial and Social Sciences, Tokushima University, Tokushima, 770-8506, Japan.
Biochem Biophys Res Commun. 2022 Jan 8;587:24-28. doi: 10.1016/j.bbrc.2021.11.089. Epub 2021 Nov 27.
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.
腔肠素(CTZ)是海洋生物中与荧光素酶(一种酶)发生发光反应的荧光素(底物),在水溶液中不稳定。CTZ 的脱氢形式(去氢腔肠素,dCTZ)稳定,被认为是 CTZ 的储存形式和从腔肠胺和 4-羟基苯丙酮酸缩合反应到 CTZ 的循环中间体。在这项研究中,在 NADH(FRase-NADH 反应)存在下,使用发光细菌 Vibrio fischeri ATCC 7744 的 NAD(P)H:FMN 氧化还原酶(FRase)成功地实现了 dCTZ 向 CTZ 的酶促转化。通过 HPLC 和 LC/ESI-TOF-MS 分析鉴定了 FRase-NADH 反应中从 dCTZ 还原的 CTZ。因此,dCTZ 可以在体外酶促转化为 CTZ。此外,通过使用与 FRase-NADH 反应偶联的 CTZ 利用荧光素酶(Gaussia 荧光素酶或 Renilla 荧光素酶)的发光活性,可以测定 dCTZ 的浓度。