首页 | 本学科首页   官方微博 | 高级检索  
     

微小毛霉凝乳酶基因的克隆与表达
引用本文:姜媛媛,王景会,李玉秋,李达,杨贞耐. 微小毛霉凝乳酶基因的克隆与表达[J]. 中国乳品工业, 2010, 38(2)
作者姓名:姜媛媛  王景会  李玉秋  李达  杨贞耐
作者单位:中国农业科技东北创新中心农产品加工研究中心,长春,130124
基金项目:吉林省科学技术厅资助项目,国家863计划探索导向项目 
摘    要:微小毛霉(Mucor pusillus)凝乳酶是微生物凝乳酶的主要来源之一,但与传统的牛凝乳酶比较具有一定的缺陷。为将其采用基因工程的方法进行改造获得理想的凝乳酶,本研究克隆到微小毛霉凝乳酶基因,将其插入原核表达载体pTWlN1中,使之与几丁质结合域(CBD)一内含肽(intein)融合,获得原核表达质粒pTWIN1/M。转化大肠杆菌BL21(DE3),后经IPTG诱导后进行SDS-PAGE电泳分析,获得了重组蛋白。

关 键 词:微小毛霉  克隆  表达

Cloning and expression of a rennet gene from mucor pusillus
JIANG Yuan-yuan,WANG Jing-hui,LI Yu-qiu,LI Da,YANG Zhen-nai. Cloning and expression of a rennet gene from mucor pusillus[J]. China Dairy Industry, 2010, 38(2)
Authors:JIANG Yuan-yuan  WANG Jing-hui  LI Yu-qiu  LI Da  YANG Zhen-nai
Affiliation:JIANG Yuan-yuan,WANG Jing-hui,LI Yu-qiu,LI Da,YANG Zhen-nai(Center of Agro-food Technology,Northeast Agricultural Research Center of China,Changchun 130124,China)
Abstract:The rennet from Mucor pusillus is one of the major sources of microbial rennet.but it hassome defects comparing with the bovine chy-mosin.In order to develop a rennet with suitable milk clotting properties,the gene of rennetwas cloned from Mucor pusillus,and the DNA frag-ment was inserted into the prokaryotic expression vector pTWIN1,forming pTWIN1/M with a fusion protein integrated with(CBD-intein).pTWIN1/M was further transformed into E.coli BL21(DE3).Expression of the enzyme was performed with IPTG induc...
Keywords:mucor pusillus  cloning  expression  
本文献已被 CNKI 万方数据 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