Marjasvaara Asse, Torvinen Mika, Kinnunen Hanne, Vainiotalo Pirjo
University of Joensuu, Department of Chemistry, Post Office Box 111, FIN-80101 Joensuu, Finland.
Biomacromolecules. 2006 May;7(5):1604-9. doi: 10.1021/bm060038p.
Enzymatic oxidation of two phenolic compounds [syringic acid (3,5-dimethoxy-4-hydroxybenzoic acid) and 2,6-dimethylphenol] was studied. The products of laccase- and laccase-mediator-catalyzed oxidation reactions were monitored by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) and further analyzed by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FTICR) MS with collision-induced dissociation (CID) experiments. For the oligomers of syringic acid, some variability was observed in MALDI-TOF analysis. However, the origin of this variability could not be resolved on the basis of MALDI-TOF spectra due to the poor resolution of the instrument in use. The strength of ESI-FTICR MS was the high-resolution data provided from oligomers of syringic acid. The CID experiments were extremely useful for structural studies of oligomers and verified that the variability of the products was due to the end groups; the phenolic hydroxyl group was modified during the oxidation.
研究了两种酚类化合物[丁香酸(3,5-二甲氧基-4-羟基苯甲酸)和2,6-二甲基苯酚]的酶促氧化反应。通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)监测漆酶和漆酶-介质催化的氧化反应产物,并通过电喷雾电离傅里叶变换离子回旋共振(ESI-FTICR)质谱和碰撞诱导解离(CID)实验进行进一步分析。对于丁香酸的低聚物,在MALDI-TOF分析中观察到一些变化。然而,由于所用仪器分辨率较差,基于MALDI-TOF光谱无法确定这种变化的来源。ESI-FTICR MS的优势在于能提供丁香酸低聚物的高分辨率数据。CID实验对低聚物的结构研究极为有用,并证实了产物的变化是由于端基造成的;酚羟基在氧化过程中发生了修饰。