首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >High-throughput functional assessment of polysaccharide-active enzymes using matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry as exemplified on plant cell wall polysaccharides
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High-throughput functional assessment of polysaccharide-active enzymes using matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry as exemplified on plant cell wall polysaccharides

机译:使用基质辅助激光解吸/电离飞行时间质谱对多糖活性酶进行高通量功能评估,以植物细胞壁多糖为例

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摘要

Despite a wealth of sequence information on genes encoding carbohydrate-active enzymes (e.g., transferases, esterases, hydrolases), very few of these enzymes have been described in detail, particularly regarding substrate specificities. A facile and rapid method for the characterization of substrate specificities of polysaccharide-active enzymes that uses matrix-assisted laser desorption-time of flight mass spectrometry (MALDI-TOF MS) has been developed. This method has been applied to characterize a xyloglucan fucosyltransferase and a pectin methyl-esterase. Reactions were performed in liquid phase, and aliquots of the reaction mixtures were spotted on a polyvinylidene fluoride (PVDF) membrane. Reaction products were precipitated onto the membrane and cleaned by treatment with an ethanol-water mixture. Subsequently, the reaction products were hydrolyzed by specific endoglycanases, and the resulting oligosaccharides were directly analyzed onto the PVDF membrane by MALDI-TOF MS. The new method is amenable to high-throughput analysis and, thus, constitutes an emerging avenue to rapidly fill the gap in our knowledge of the specificities of polysaccharide-active enzymes. (c) 2007 Elsevier Inc. All rights reserved.
机译:尽管编码碳水化合物活性酶(例如,转移酶,酯酶,水解酶)的基因有大量的序列信息,但很少详细描述这些酶,特别是关于底物特异性。已经开发了一种简便快速的表征多糖活性酶底物特异性的方法,该方法使用基质辅助激光解吸-飞行时间质谱(MALDI-TOF MS)。该方法已用于表征木葡聚糖岩藻糖基转移酶和果胶甲基酯酶。反应在液相中进行,并将反应混合物的等分试样点在聚偏二氟乙烯(PVDF)膜上。反应产物沉淀在膜上,并通过用乙醇-水混合物处理进行清洁。随后,反应产物被特定的内切葡聚糖酶水解,所得的低聚糖通过MALDI-TOF MS直接分析到PVDF膜上。这种新方法适用于高通量分析,因此构成了一种新兴途径,可以迅速填补我们对多糖活性酶特异性的了解。 (c)2007 Elsevier Inc.保留所有权利。

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