首页> 外文期刊>Journal of Analytical & Applied Pyrolysis >The effect of enzymatic removal of proteins from plant leaf material as studied by pyrolysis-mass spectrometry: detection of additional protein marker fragment ions
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The effect of enzymatic removal of proteins from plant leaf material as studied by pyrolysis-mass spectrometry: detection of additional protein marker fragment ions

机译:通过热解质谱法研究从植物叶片材料中酶去除蛋白质的影响:检测其他蛋白质标记片段离子

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This analytical pyrolysis study investigates the effects of ethanol extraction and of enzymatic protein removal from leaf material of two grass species, Poa annua and Poa pratensis. After pyrolysis the leaf fragments were analysed by low-voltage electron impact (El) and by ammonia chemical ionization (NH_3-Cl). Pronase-treated and untreated material were compared using multivariate analysis of the PyMS data. The resulting discriminant function spectra among others show a kind of 'negative image' of the PyMS spectrum of the plant proteins originally present in Poa leaves. In addition to known protein marker fragment ions several hithertoo unrecognised ones were apparent as well. The nitrogen concentration was determined for several plant fractions. Quantitative comparison of relative intensities of masses found by discriminant analysis led to selection of an additional group of protein marker fragments (m/z 54, 70, 84, 107, 130, 209, 225 and 243 for El and 70, 72, 75, 84, 86, 89, 125, 131, 136, 146, 165, 201, 226, 229, 244, 262, 281 and 295 for NH_3-Cl) which showed a significant correlation (r~2 > 0.5) with the total nitrogen content in the Poa leaves. The origin of grass protein marker fragments was discussed in comparison with reference spectra of two new plant cell-wall proteins, a synthetic polyamine and of albumin. Enzymatic digestion, in addition, yielded a better exposure of the plant cell-wall skeleton, and, therefore, also of the biomacromolecule lignin. Using previously obtained wet chemical data response values were calculated for marker fragments comparative to the analysed content of proteins, polysaccharides and different lignins.
机译:这项分析热解研究研究了乙醇提取和从两种草(Poa annua和Poa pratensis)的叶片材料中去除酶蛋白的影响。热解后,通过低压电子撞击(El)和氨化学电离(NH_3-Cl)分析叶片碎片。使用PyMS数据的多变量分析比较了经链酶处理的材料和未经处理的材料。由此产生的判别功能谱显示了最初存在于Poa叶中的植物蛋白的PyMS谱的一种“负像”。除已知的蛋白质标记片段离子外,其他一些迄今为止也无法识别的离子也很明显。测定几种植物馏分的氮浓度。通过判别分析发现的相对质量的定量比较导致选择了另一组蛋白质标记片段(E / m为54、70、84、107、130、209、225和243,El和70、72、75, NH_3-Cl的84、86、89、125、131、136、146、165、201、226、229、244、262、281和295)与总氮呈显着相关性(r〜2> 0.5)内容在Poa叶子中。与两种新的植物细胞壁蛋白(一种合成的多胺和白蛋白)的参考光谱相比较,讨论了草蛋白标记片段的起源。另外,酶消化产生了更好的植物细胞壁骨架的暴露,因此也获得了生物大分子木质素的暴露。使用先前获得的湿化学数据,可计算出标记片段的响应值,与蛋白质,多糖和不同木质素的分析含量进行比较。

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