首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning arg3 the gene for ornithine carbamoyltransferase from Saccharomyces cerevisiae: expression in Escherichia coli requires secondary mutations; production of plasmid beta-lactamase in yeast.
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Cloning arg3 the gene for ornithine carbamoyltransferase from Saccharomyces cerevisiae: expression in Escherichia coli requires secondary mutations; production of plasmid beta-lactamase in yeast.

机译:从酿酒酵母中克隆鸟氨酸氨基甲酰基转移酶基因arg3:在大肠杆菌中的表达需要二次突变。酵母中产生质粒β-内酰胺酶。

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摘要

The yeast arg3 gene, coding for ornithine carbamoyltransferase (carbamoylphosphate:L-ornithine carbamoyltransferase, EC 2.1.3.3), has been cloned on a hybrid pBR322-2-micrometers plasmid. The cloned gene gives a normal regulatory response in yeast. It is not expressed at 35 degrees C when a mutation preventing mRNA export from the nucleus at this temperature is included in the genetic make-up of the carrier strain. In Escherichia coli, no functional expression can be observed from the native yeast arg3 gene. The study of a mutant plasmid (M1) producing low levels of yeast carbamoyltransferase in E. coli has permitted the localization and orientation of arg3 on the plasmid. The mutation involved is a deletion that alters the regulatory response of arg3 in yeast. The plasmid bla gene produces detectable amounts of beta-lactamase (penicillin amido-beta-lactamhydrolase, EC 3.5.2.6) in yeast: the data provide an estimate of the beta-lactamase activity associated with one exemplar of the plasmid expressing arg3 (0.6 units).
机译:已将编码鸟氨酸氨基甲酰基转移酶(氨基甲酰基磷酸酯:L-鸟氨酸氨基甲酰基转移酶,EC 2.1.3.3)的酵母arg3基因克隆到pBR322-2-microbi杂交质粒上。克隆的基因在酵母中产生正常的调节反应。当在该温度下阻止突变mRNA从细胞核中输出的突变被包括在载体菌株的基因组成中时,它在35摄氏度下不会表达。在大肠杆菌中,无法从天然酵母arg3基因中观察到功能性表达。对在大肠杆菌中产生低水平酵母氨甲酰转移酶的突变质粒(M1)的研究,使arg3在质粒上的定位和方向得以实现。涉及的突变是缺失,其改变了酵母中arg3的调节反应。质粒bla基因在酵母中产生可检测量的β-内酰胺酶(青霉素酰胺基β-内酰胺水解酶,EC 3.5.2.6):数据提供了与表达arg3(0.6个单位)的一个示例质粒相关的β-内酰胺酶活性的估计值)。

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