首页 | 本学科首页   官方微博 | 高级检索  
     


Chemical Modification and Fluorescence Spectrum of Tryptophan Residues in Pullulanase
Authors:Li-rong TENG   Hao FAN   Yuan-yuan ZHANG   Qi YU   Yue-feng HUANG  Lan-ying LIU  
Affiliation:College of Life Science, Jilin University, Changchun 130023, P. R. China
Abstract:Tryptophan(Trp) residues in a pullulanase were modified by N-bromosuccinimide(NBS). The results of the Spande method indicate that there are 18 Trp residues in the pullulanase and nine of them are located on the surface of the enzyme. Three of these Trp residues are nonessential residues which show the fastest reaction rate according to the Zou′s plot. Two of the seven relative faster reacting residues are essential for the activity of the enzyme. The other eight are the slowest in the reaction rate or non-reactive residues for the reaction. The fluorescence and circular dichroism(CD) spectra of the pullulanase have been changed after the reaction with NBS. Potassium iodide(KI) and acrylamide also have remarkable influences on the fluorescence spectra of the pullulanase.
Keywords:Pullulanase  Tryptophan(Trp)  Chemical modification  Fluorescence spectrum  
本文献已被 CNKI 维普 万方数据 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号