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酸性或十二烷基硫酸钠电泳后,聚丙烯酰胺凝胶上果胶酯酶的活性染色。

Activity staining of pectinesterase on polyacrylamide gels after acidic or sodium dodecyl sulfate electrophoresis.

作者信息

Hou W C, Lin Y H

机构信息

Institute of Botany, Academica Sinica, Nankang, Taipei, Taiwan, ROC.

出版信息

Electrophoresis. 1998 May;19(5):692-4. doi: 10.1002/elps.1150190515.

Abstract

Pectinesterase (PE), from commercial orange peels or ammonium sulfate fractionation (50-80% saturation) of pea pods, was detected on polyacrylamide gels after native acidic polyacrylamide gel electrophoresis (PAGE) or sodium dodecyl sulfate (SDS)-PAGE by using the synthetic substrate beta-naphthyl acetate (beta-NA). The release of beta-naphthol (at 322 nm) from beta-NA was proportional to PE activity. The PE activity bands on polyacrylamide gels after native acidic PAGE or SDS-PAGE were stained with a combination of tetrazotized o-dianisidine and beta-NA. This fast and sensitive method can be used for enzyme purification and characterization.

摘要

通过使用合成底物β-萘乙酸(β-NA),在天然酸性聚丙烯酰胺凝胶电泳(PAGE)或十二烷基硫酸钠(SDS)-PAGE后,在聚丙烯酰胺凝胶上检测了来自商业橙皮或豌豆荚硫酸铵分级分离(50-80%饱和度)的果胶酯酶(PE)。β-萘酚从β-NA的释放(在322nm处)与PE活性成正比。天然酸性PAGE或SDS-PAGE后聚丙烯酰胺凝胶上的PE活性带用重氮二茴香胺和β-NA的组合染色。这种快速灵敏的方法可用于酶的纯化和表征。

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