首页> 外文期刊>Analytical and bioanalytical chemistry >Structure elucidation of the thermal degradation products of the nucleotide cofactors NADH and NADPH by nano-ESI-FTICR-MS and HPLC-MS
【24h】

Structure elucidation of the thermal degradation products of the nucleotide cofactors NADH and NADPH by nano-ESI-FTICR-MS and HPLC-MS

机译:纳米ESI-FTICR-MS和HPLC-MS阐明核苷酸辅因子NADH和NADPH的热降解产物的结构

获取原文
获取原文并翻译 | 示例
           

摘要

Redox cofactors like NADH and NADPH are essential for the catalytic activity of several oxidoreductases. Here, we describe a comparative study of the thermal degradation products of both cofactors in the dry and liquid states. The degradation products were first separated, detected, and quantified by high-performance liquid chromatography (HPLC). Subsequently, selected main fractions were investigated by nanoelectrospray ionization-Fourier transform ion cyclotron resonance mass spectrometry (MS). Additionally, HPLC-MS was used to elucidate the structure of all degradation products. From these data, degradation pathways for both the liquid and the solid states were elucidated. Thermal degradation in water is significantly faster compared to degradation in the solid state. Hydrolysis and oxidative ring opening of the reduced nicotinamide adenine dinucleotide (phosphate) were shown to be the main reaction paths. Surprisingly, no significant differences were observed between the degradation of both cofactors in solution and in the solid state. Our results demonstrate that the stability of both cofactors is not limiting at moderate temperatures if they are used in the dry state (e.g., solid/gas catalysis). Significant degradation of dry cofactors was only observed under conditions, which are usually not appropriate for biocatalysis (>95 °C). Besides, the situation is completely different in solution where degradation is already observed at moderate temperatures.
机译:氧化还原辅助因子(如NADH和NADPH)对于几种氧化还原酶的催化活性至关重要。在这里,我们描述了干燥和液态两种辅因子的热降解产物的比较研究。首先通过高效液相色谱(HPLC)对降解产物进行分离,检测和定量。随后,通过纳米电喷雾电离-傅立叶变换离子回旋共振质谱(MS)研究选定的主要馏分。此外,HPLC-MS用于阐明所有降解产物的结构。从这些数据,阐明了液态和固态的降解途径。与固态降解相比,水中的热降解明显更快。还原的烟酰胺腺嘌呤二核苷酸(磷酸)的水解和氧化性开环被证明是主要的反应路径。出人意料的是,溶液和固态中的两种辅因子的降解之间均未观察到显着差异。我们的结果表明,如果在干燥状态下使用两种辅助因子(例如,固体/气体催化),则它们在中等温度下的稳定性不受限制。仅在通常不适合生物催化(> 95°C)的条件下观察到干辅因子的显着降解。此外,在中等温度下已经观察到降解的溶液情况完全不同。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号