Mort A J, Chen E M
Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater 74078-3035, USA.
Electrophoresis. 1996 Feb;17(2):379-83. doi: 10.1002/elps.1150170215.
Slight modifications of published procedures (Stefansson, M. and Novotny, M., Carbohydr. Res. 1994, 258 1-9) allow separation by relative size of 8-amino-naphthalene-1,3,6-trisulfonate (ANTS)-labeled neutral and acidic oligosaccharides by electrophoresis in uncoated capillaries. The separations are performed at pH 2.5 to suppress both any charge from carboxylic acid groups on the oligosaccharides and electroosmotic flow. Utility of the procedure is demonstrated by its application to characterization of substrate specificity of endopolygalacturonases. The results show that both a fungal and a bacterial endopolygalacturonase need four adjacent nonesterified galacturonic acid residues in a pectin to be able to act.
对已发表方法(斯特凡松,M.和诺沃特尼,M.,《碳水化合物研究》,1994年,258卷,1 - 9页)进行轻微修改后,可通过在未涂层毛细管中进行电泳,按相对大小分离8 - 氨基萘 - 1,3,6 - 三磺酸盐(ANTS)标记的中性和酸性寡糖。分离在pH 2.5下进行,以抑制寡糖上羧酸基团的任何电荷以及电渗流。该方法的实用性通过其在表征内切多聚半乳糖醛酸酶底物特异性方面的应用得到证明。结果表明,一种真菌内切多聚半乳糖醛酸酶和一种细菌内切多聚半乳糖醛酸酶都需要果胶中有四个相邻的非酯化半乳糖醛酸残基才能起作用。