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Fructose bisphosphatase of Escherichia coli: cloning of the structural gene (fbp) and preparation of a chromosomal deletion.

机译:大肠杆菌的果糖双磷酸酶:结构基因(fbp)的克隆和染色体缺失的制备。

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摘要

The fbp locus at 96 min on the Escherichia coli chromosome governs fructose bisphosphatase (fructose-1,6-P2 1-phosphatase). We have cloned and subcloned fbp on vector pBR322 to obtain strains with high levels of the enzyme. In vivo mutagenesis of the clone was used to show that fbp is the structural gene. The gene was deleted on the plasmid in vitro, and the chromosomal wild-type locus was replaced with this deletion by a method involving stabilization of a heterozygous intermediate resulting from plasmid integration, followed by segregation of the wild-type gene.
机译:大肠杆菌染色体上96分钟的fbp位点控制着果糖双磷酸酶(果糖1,6-P2 1-磷酸酶)。我们已经在载体pBR322上克隆并亚克隆了fbp,以获得具有高水平酶的菌株。克隆的体内诱变被用来显示fbp是结构基因。该基因在体外在质粒上缺失,并通过涉及稳定因质粒整合产生的杂合中间体,然后分离野生型基因的方法,用该缺失替换染色体野生型基因座。

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