详细信息
文献类型:期刊文献
中文题名:relA基因在重组大肠杆菌BL21合成嘌呤核苷磷酸化酶作用研究
英文题名:Function of relA gene in production of PNPase in E.coli BL21
作者:段纪甫[1];高黎荣[1];李江[1];付水林[1];宫衡[1]
机构:[1]华东理工大学生物反应器工程国家重点实验室,上海200237
年份:2014
卷号:44
期号:3
起止页码:30
中文期刊名:工业微生物
外文期刊名:Industrial Microbiology
收录:CSCD:【CSCD_E2013_2014】;
语种:中文
中文关键词:大肠杆菌;Red重组;relA基因;嘌呤核苷磷酸化酶
外文关键词:E. coli; Red recombination ; relA ; PNPase
摘要:利用Red同源重组技术敲除大肠杆菌BL21中relA基因,获得△relA突变株。进一步研究表明在LB复合培养中relA基因对大肠杆菌的生长几乎没有明显影响,但是对其重组蛋白的合成有着较大的影响:降低了25%。结果表明,relA基因在大肠杆菌表达重组蛋白方面有着较重要的作用。
The Red recombination system was used to knock out the relA gene in E. coli BL21 and then the ArelA mutant was obtained. Further study was conducted and results showed that the relA gene had no effect on its growth while significant difference in terms of synthesis of recombinant protein was found between these two strains. It reduced by 25 % compared with the original strain. Results showed that the relA gene may play an important role in synthesis of recombinant protein in E. coli BI21.
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