首页> 外国专利> Method of expression of genes under nitrogen deficiency - pref. using the glutamine synthetase promoter 2 of E.coli and ammonium and/or glutamine as limiting nitrogen source

Method of expression of genes under nitrogen deficiency - pref. using the glutamine synthetase promoter 2 of E.coli and ammonium and/or glutamine as limiting nitrogen source

机译:氮缺乏时基因表达的方法-优选使用大肠杆菌的谷氨酰胺合成酶启动子2和铵和/或谷氨酰胺作为限制氮源

摘要

Method for the expression of recombinant structural genes in E.coli under the control of A promoter that is regulatable by a nitrogen source, the cells being fermented under nitrogen deficiency conditions. Pref., the promoter is the glutamine synthetase promoter 2 of E.coli (glnAP2) or DNA of similar length (+/- 10%) hybridising at 1 M NaCl at 50 deg.C with it. The E.coli strain, pref. TG1, in at least part of its growth phase is subjected to nitrogen deficiency, wherein the limiting nitrogen source may be ammonium and/or glutamine. Also claimed is an expression vector of the above features and E.coli contg. such a vector. USE/ADVANTAGE - In contrast to the prior art the vector described allows a cheap and simple induction of the promoter which is partic. useful in large scale fermenters used in biotechnolog
机译:在由氮源调节的A启动子的控制下在大肠杆菌中表达重组结构基因的方法,该细胞在氮缺乏条件下发酵。优选地,该启动子是大肠杆菌的谷氨酰胺合成酶启动子2(glnAP2)或相似长度(+/- 10%)的DNA在50℃在1M NaCl下杂交。大肠杆菌菌株,优选。 TG1在其至少部分的生长期遭受氮缺乏,其中极限氮源可以是铵和/或谷氨酰胺。还要求保护具有上述特征和大肠杆菌的表达载体。这样的载体。使用/优点-与现有技术相反,所述载体允许廉价且简单地诱导部分启动子。在生物技术中使用的大型发酵罐中有用

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