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利用exu质粒对exuT和uxaC操纵基因进行物理图谱分析并在体外构建缺失突变体。

Physical mapping of the exuT and uxaC operators by use of exu plasmids and generation of deletion mutants in vitro.

作者信息

Mata-Gilsinger M, Ritzenthaler P

出版信息

J Bacteriol. 1983 Sep;155(3):973-82. doi: 10.1128/jb.155.3.973-982.1983.

Abstract

Operons uxaCA and exuT of the hexuronate system are very closely linked on the Escherichia coli genetic map. Using plasmid vectors constructed by Casadaban et al. (J. Bacteriol. 143:971-980, 1980), we formed exuT-lacZ and uxaA-lacZ fusions in vitro. The phenotypic properties of the new plasmids allowed us to confirm that the exuT and uxaCA operons are divergently transcribed. An analysis of these fusion plasmids and derivatives in the presence of multiple copies of the exuR regulatory gene demonstrated that the two operons possess separate control regions. The precise location of the operator site relative to endonuclease restriction sites was determined. In addition, deletions of different lengths were generated on exu plasmids by restriction enzymes and were recombined into the chromosome. The expression of the exu regulon genes in the resulting deletion mutants is in agreement with the postulated location of the exuT and uxaCA operators in the fusion plasmids.

摘要

己糖醛酸系统的操纵子uxaCA和exuT在大肠杆菌遗传图谱上紧密相连。利用卡萨达班等人构建的质粒载体(《细菌学杂志》143:971 - 980,1980年),我们在体外构建了exuT - lacZ和uxaA - lacZ融合体。新质粒的表型特性使我们能够确认exuT和uxaCA操纵子是反向转录的。在存在多个exuR调控基因拷贝的情况下对这些融合质粒及其衍生物进行分析表明,这两个操纵子拥有各自独立的控制区域。确定了操纵位点相对于核酸内切酶限制位点的精确位置。此外,通过限制酶在exu质粒上产生不同长度的缺失,并将其重组到染色体中。在所得缺失突变体中exu调节子基因的表达与融合质粒中exuT和uxaCA操纵位点的假定位置相符。

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