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克隆酿酒酵母鸟氨酸氨甲酰基转移酶基因arg3:在大肠杆菌中的表达需要二次突变;酵母中质粒β-内酰胺酶的产生

Cloning arg3, the gene for ornithine carbamoyltransferase from Saccharomyces cerevisiae: expression in Escherichia coli requires secondary mutations; production of plasmid beta-lactamase in yeast.

作者信息

Crabeel M, Messenguy F, Lacroute F, Glansdorff N

出版信息

Proc Natl Acad Sci U S A. 1981 Aug;78(8):5026-30. doi: 10.1073/pnas.78.8.5026.

Abstract

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).

摘要

酵母arg3基因编码鸟氨酸氨甲酰基转移酶(氨甲酰磷酸:L-鸟氨酸氨甲酰基转移酶,EC 2.1.3.3),已被克隆到一个pBR322-2-微米杂种质粒上。克隆的基因在酵母中呈现正常的调节反应。当载体菌株的遗传组成中包含一个在35℃时阻止mRNA从细胞核输出的突变时,该基因在35℃下不表达。在大肠杆菌中,未观察到天然酵母arg3基因的功能性表达。对在大肠杆菌中产生低水平酵母氨甲酰基转移酶的突变体质粒(M1)的研究,已确定了arg3在质粒上的定位和方向。所涉及的突变是一个缺失,它改变了arg3在酵母中的调节反应。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-β-内酰胺水解酶,EC 3.5.2.6):这些数据提供了与表达arg3的一种质粒样品相关的β-内酰胺酶活性的估计值(0.6单位)。

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