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工程菌人溶菌酶的纯化和性质
引用本文:叶军 钱世钧. 工程菌人溶菌酶的纯化和性质[J]. 微生物学报, 1999, 39(1): 55-59
作者姓名:叶军 钱世钧
作者单位:中国科学院微生物研究所 北京 100080
基金项目:“八五”国家科技攻关项目
摘    要:将人溶菌酶工程菌株在发酵培养、菌体经超声破碎、变性和复性后所得的粗酶液经ExpressIon S阳离子交换柱层析,得到电泳纯的酶,比活达到48KG*4]000u/mg。此酶的最适pH为6.5;等电点为8.91;对溶壁微球菌的米氏常数Km=0.0311mg/mL;60℃保温30〖KG*4]min,酶活力剩余48.3%。N末端氨基酸序列除了第一个Met,其余4个与预期相符。一些重金属离子对酶的活性影响不尽相同,在0.01

关 键 词:重组人溶菌酶,纯化,性质

PURIFICATION AND PROPERTIES OF HUMAN LYSOZYME IN ENGINEERED BACTERIUM E.COLI *
Ye Jun Qian Shijun. PURIFICATION AND PROPERTIES OF HUMAN LYSOZYME IN ENGINEERED BACTERIUM E.COLI *[J]. Acta microbiologica Sinica, 1999, 39(1): 55-59
Authors:Ye Jun Qian Shijun
Affiliation:Institute of Microbiology, Chinese Academy of Sciences, Beijing 100080.
Abstract:To obtain the SDS-PAGE-pure human lysozyme, the crude enzyme of engineered bacterium E. coli was purified by chromatography on cation ion exchange of Express-Ion S. The optimum reaction temperature and pH of this lysozyme were 45 degrees C and 6.5, respectively. The isoelectric point is pH 8.91, and Km of the enzyme for Micrococcus lysodeikticus is 0.0311 mg/mL. The thermal stability of the engineered enzyme is more sensible than hen egg white lysozyme and human milk lysozyme. The sequence of 5 amino acids in N-end is same as designed, except an Met at the first. The affects of some metal ion on this enzyme were shown. Cu2+ of 0.01 mmol/L could completely inactivate the enzyme.
Keywords:Recombinant Human lysozyme  Purification  Properties
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