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大肠杆菌K12中铁调节系统阻遏蛋白基因的克隆

Cloning of the repressor protein gene of iron-regulated systems in Escherichia coli K12.

作者信息

Hantke K

出版信息

Mol Gen Genet. 1984;197(2):337-41. doi: 10.1007/BF00330982.

Abstract

In Escherichia coli the iron uptake systems are regulated by the fur gene product. The synthesis of the outer membrane proteins fiu, fepA, fecA, fhuA, fhuE and cir is derepressed at low iron concentrations in the medium or constitutive in a fur mutant. The fur gene region cloned into pACYC184 was analysed by restriction analysis, Tn1000 mutagenesis and complementation studies. The presence of fur+ plasmids repressed synthesis of the proteins fepA, fecA, fhuE and cir in a chromosomal fur mutant. More quantitatively, the repression to wild-type levels was shown with lac fusions to the genes fiu, fepA and cir. In minicells an 18,000 dalton protein was identified as the fur gene product. Correlated with the fur protein a slightly smaller protein, possibly a degradation product, was observed. The gene fur was mapped on the E. coli chromosome near nagA at about 15.5 min.

摘要

在大肠杆菌中,铁摄取系统受fur基因产物调控。外膜蛋白fiu、fepA、fecA、fhuA、fhuE和cir的合成在培养基中铁浓度较低时去阻遏,或在fur突变体中组成型表达。对克隆到pACYC184中的fur基因区域进行了限制性分析、Tn1000诱变和互补研究。fur+质粒的存在抑制了染色体fur突变体中fepA、fecA、fhuE和cir蛋白的合成。更定量地说,通过与fiu基因、fepA基因和cir基因的lac融合,显示出抑制作用达到野生型水平。在微小细胞中,一种18,000道尔顿的蛋白质被鉴定为fur基因产物。与fur蛋白相关的是,观察到一种稍小的蛋白质,可能是一种降解产物。fur基因定位于大肠杆菌染色体上nagA附近,约在15.5分钟处。

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