首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Production of Two Novel Methoxy-Isoflavones from Biotransformation of 8-Hydroxydaidzein by Recombinant Escherichia coli Expressing O-Methyltransferase SpOMT2884 from Streptomyces peucetius
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Production of Two Novel Methoxy-Isoflavones from Biotransformation of 8-Hydroxydaidzein by Recombinant Escherichia coli Expressing O-Methyltransferase SpOMT2884 from Streptomyces peucetius

机译:从表达链霉菌的O-甲基转移酶SpOMT2884的重组大肠杆菌经8-羟基黄豆苷原的生物转化生产两种新型甲氧基-异黄酮。

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摘要

Biotransformation of 8-hydroxydaidzein by recombinant Escherichia coli expressing O-methyltransferase (OMT) SpOMT2884 from Streptomyces peucetius was investigated. Two metabolites were isolated and identified as 7,4′-dihydroxy-8-methoxy-isoflavone (>1) and 8,4′-dihydroxy-7-methoxy-isoflavone (>2), based on mass, 1H-nuclear magnetic resonance (NMR) and 13C-NMR spectrophotometric analysis. The maximum production yields of compound (>1) and (>2) in a 5-L fermenter were 9.3 mg/L and 6.0 mg/L, respectively. The two methoxy-isoflavones showed dose-dependent inhibitory effects on melanogenesis in cultured B16 melanoma cells under non-toxic conditions. Among the effects, compound (>1) decreased melanogenesis to 63.5% of the control at 25 μM. This is the first report on the 8-O-methylation activity of OMT toward isoflavones. In addition, the present study also first identified compound (>1) with potent melanogenesis inhibitory activity.
机译:研究了表达来自Peuceomyces peucetius的O-甲基转移酶(OMT)SpOMT2884的重组大肠杆菌对8-羟基黄豆苷元的生物转化。分离出两种代谢物,鉴定为7,4'-二羟基-8-甲氧基-异黄酮(> 1 )和8,4'-二羟基-7-甲氧基-异黄酮(> 2 ),基于质量,进行1H核磁共振(NMR)和13C-NMR分光光度法分析。在5升发酵罐中,化合物(> 1 )和(> 2 )的最大产量分别为9.3 mg / L和6.0 mg / L。两种甲氧基异黄酮在无毒条件下对培养的B16黑色素瘤细胞中的黑色素生成显示出剂量依赖性抑制作用。在这些效应中,化合物(> 1 )在25μM时将黑色素生成减少至对照的63.5%。这是有关OMT对异黄酮的8-O-甲基化活性的首次报道。此外,本研究还首先鉴定了具有有效抑制黑色素生成活性的化合物(> 1 )。

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