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首页> 外文期刊>Journal of bacteriology >Dominance relationships among mutant alleles of regulatory gene araC in the Escherichia coli B/R L-arabinose operon.
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Dominance relationships among mutant alleles of regulatory gene araC in the Escherichia coli B/R L-arabinose operon.

机译:大肠杆菌B / R L-阿拉伯糖操纵子中调控基因araC突变等位基因之间的优势关系。

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The araBAD operon of Escherichia coli B/r is positively and negatively regulated by the araC+ regulatory protein. Mutations in gene araC can result in a variety of different regulatory phenotypes: araC null mutants (those carrying a null allele exhibiting no repressor or activator activity) are unable to achieve operon induction; araC-constitutive (araCc) mutants are partially constitutive, inducible by D-fucose, and resistant to catabolite repression; araCh mutants are hypersensitive to catabolite repression; and araCi mutants are resistant to catabolite repression. Various mutant alleles of gene araC were cloned into a derivative of plasmid pBR322 by in vivo recombination. Various heterozygous araC allelic combinations were constructed by transformation. Analysis of isomerase (araA) specific activity levels under various growth conditions indicated the following dominance relationships with regard to sensitivity to catabolite repression: araCh greater than araC+ greater than (araCc and araCi) greater than araC. It was concluded that the araCh protein may form a repressor complex that is refractory to removal by cyclic AMP receptor protein-cyclic AMP complex. This was interpreted in terms of the known nucleoprotein interactions between ara regulatory proteins and ara regulatory DNA.
机译:大肠杆菌B / r的araBAD操纵子受到araC +调节蛋白的正向和负向调节。 araC基因的突变可导致多种不同的调节表型:araC无效突变体(携带无效等位基因且不表现阻遏物或激活剂活性的无效突变体)无法实现操纵子诱导。 araC组成型(araCc)突变体是部分组成型的,可被D-岩藻糖诱导,并且对分解代谢物的抑制具有抗性。 araCh突变体对分解代谢物抑制高度敏感; araCi和araCi突变体对分解代谢物阻遏具有抗性。通过体内重组将araC基因的各种突变等位基因克隆到质粒pBR322的衍生物中。通过转化构建了各种杂合的araC等位基因组合。对各种生长条件下的异构酶(araA)比活水平的分析表明,对分解代谢物阻抑的敏感性具有以下优势关系:araCh大于araC +大于(araCc和araCi)大于araC。得出的结论是,araCh蛋白可能形成阻遏物复合物,该复合物对于通过环AMP受体蛋白-环AMP复合物的去除是难以耐受的。这是根据ara调节蛋白和ara调节DNA之间已知的核蛋白相互作用来解释的。

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