首页 | 本学科首页   官方微博 | 高级检索  
   检索      

蜂房哈夫尼菌植酸酶基因appA的克隆、表达及酶学性质研究
引用本文:谷维娜,黄火清,杨培龙,罗会颖,孟昆,王亚茹,姚斌.蜂房哈夫尼菌植酸酶基因appA的克隆、表达及酶学性质研究[J].生物工程学报,2007,23(6):1017-1021.
作者姓名:谷维娜  黄火清  杨培龙  罗会颖  孟昆  王亚茹  姚斌
作者单位:中国农业科学院饲料研究所,北京,100081
基金项目:国家高技术研究发展计划(863计划)
摘    要:从蜂房哈夫尼菌(Hafniaalvei)中克隆获得一个植酸酶编码基因appA,该基因全长1335bp,编码444个氨基酸,其中前33个氨基酸为信号肽,成熟蛋白的理论分子量为45.2kD。将基因appA克隆到大肠杆菌E.coli表达载体pET-22b( ),并在大肠杆菌中表达,表达产物具有植酸酶活性。对表达的酶蛋白进行纯化,并初步研究了该酶的酶学性质,结果表明:酶的作用最适pH值为4.5;在pH2.0~10.0范围内,酶活性保留80%以上;酶的作用最适温度为60℃;酶的比活性为356.7U/mg,酶动力学分析表明其Km为0.49mmol/L,Vmax为238U/mg;该酶对胰蛋白酶和胃蛋白酶有一定的抗性。该研究为哈夫尼菌属来源植酸酶的首次报道。

关 键 词:植酸酶  基因表达  纯化  酶学性质
文章编号:1000-3061(2007)06-1017-05
修稿时间:2007年3月16日

Gene Cloning, Expression and Characterization of a Novel Phytase from Hafnia alvei
GU Wei-Na,HUANG Huo-Qing,YANG Pei-Long,LUO Hui-Ying,MENG Kun,WANG Ya-Ru,YAO Bin.Gene Cloning, Expression and Characterization of a Novel Phytase from Hafnia alvei[J].Chinese Journal of Biotechnology,2007,23(6):1017-1021.
Authors:GU Wei-Na  HUANG Huo-Qing  YANG Pei-Long  LUO Hui-Ying  MENG Kun  WANG Ya-Ru  YAO Bin
Institution:Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Abstract:A gene appA encoding a novel phytase was firstly cloned from Hafnia alvei by PCR and sequenced. The gene was consisted of 1335 bp, encoding 444 amino acids. The calculated molecular weight of the mature APPA was about 45.2 kD. The gene appA was expressed in E. coli BL21 (DE3). Recombinant APPA was purified and its enzymatic properties were determined. The optimum pH for the enzyme was 4.5 and the optimum temperature was 60 degrees C. The pH stability of r-APPA is good, the relative phytase activity was above 80% after treated in buffers of pH 2.0-10.0. The specific activity of r-APPA is 356.7 U/mg, and the Km value was 0.49 mmol/L and Vmax of 238 U/mg. The enzyme showed resistance to pepsin and trypsin treatment.
Keywords:phytase  overexpression  purification  charaterization
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《生物工程学报》浏览原始摘要信息
点击此处可从《生物工程学报》下载免费的PDF全文
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