Department of Chemistry, Graduate School of Science,Nagoya University, Furo-cho, Chikusa-ku,Nagoya 464-8602, Japan.
J Biol Inorg Chem. 2010 Sep;15(7):1109-15. doi: 10.1007/s00775-010-0671-9. Epub 2010 May 19.
Aromatic C-H bond hydroxylation of 1-methoxynaphthalene was efficiently catalyzed by the substrate misrecognition system of the hydrogen peroxide dependent cytochrome P450BSbeta (CYP152A1), which usually catalyzes hydroxylation of long-alkyl-chain fatty acids. Very importantly, the hydroxylation of 1-methoxynaphthalene can be monitored by a color change since the formation of 4-methoxy-1-naphthol was immediately followed by its further oxidation to yield Russig's blue. Russig's blue formation allows us to estimate the peroxygenation activity of enzymes without the use of high performance liquid chromatography, gas chromatography, and nuclear magnetic resonance measurements.
1-甲氧基萘的芳族 C-H 键羟化反应被依赖过氧化氢的细胞色素 P450BSβ(CYP152A1)的底物错误识别系统高效催化,该系统通常催化长链脂肪酸的羟化反应。非常重要的是,由于 4-甲氧基-1-萘酚的形成立即伴随着其进一步氧化生成 Russig's 蓝,因此可以通过颜色变化监测 1-甲氧基萘的羟化反应。Russig's 蓝的形成使我们能够在不使用高效液相色谱、气相色谱和核磁共振测量的情况下估计过氧化物酶的过氧酶活性。