Leboeuf Edouard, Immerzeel Peter, Gibon Yves, Steup Martin, Pauly Markus
Department of Plant Physiology, Institute of Biochemistry and Biology, University of Potsdam, D-14476 Potsdam-Golm, Germany.
Anal Biochem. 2008 Feb 1;373(1):9-17. doi: 10.1016/j.ab.2007.10.007. Epub 2007 Oct 11.
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.
尽管有大量关于编码碳水化合物活性酶(如转移酶、酯酶、水解酶)的基因的序列信息,但对这些酶的详细描述却很少,尤其是在底物特异性方面。已经开发出一种简便快速的方法,用于表征多糖活性酶的底物特异性,该方法使用基质辅助激光解吸飞行时间质谱(MALDI-TOF MS)。此方法已应用于表征一种木葡聚糖岩藻糖基转移酶和一种果胶甲基酯酶。反应在液相中进行,将反应混合物的等分试样点样在聚偏二氟乙烯(PVDF)膜上。反应产物沉淀在膜上,并用乙醇-水混合物处理进行清洗。随后,反应产物用特定的内切聚糖酶水解,所得寡糖通过MALDI-TOF MS直接在PVDF膜上进行分析。这种新方法适用于高通量分析,因此构成了一条迅速填补我们在多糖活性酶特异性知识方面空白的新途径。