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Crosstalk of Escherichia coli FadR with Global Regulators in Expression of Fatty Acid Transport Genes

机译:在脂肪酸转运基因的表达与全球监管机构大肠杆菌飞达串扰

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摘要

Escherichia coli FadR plays two regulatory roles in fatty acid metabolism. FadR represses the fatty acid degradation (fad) system and activates the unsaturated fatty acid synthetic pathway. Cross-talk between E. coli FadR and the ArcA-ArcB oxygen-responsive two-component system was observed that resulted in diverse regulation of certain fad regulon β-oxidation genes. We have extended such analyses to the fadL and fadD genes, the protein products of which are required for long chain fatty acid transport and have also studied the role of a third global regulator, the CRP-cAMP complex. The promoters of both the fadL and fadD genes contain two experimentally validated FadR-binding sites plus binding sites for ArcA and CRP-cAMP. Despite the presence of dual binding sites FadR only modestly regulates expression of these genes, indicating that the number of binding sites does not determine regulatory strength. We report complementary in vitro and in vivo studies indicating that the CRP-cAMP complex directly activates expression of fadL and fadD as well as the β-oxidation gene, fadH. The physiological relevance of the fadL and fadD transcription data was validated by direct assays of long chain fatty acid transport.
机译:大肠杆菌FadR在脂肪酸代谢中起两个调节作用。 FadR抑制脂肪酸降解(fad)系统并激活不饱和脂肪酸合成途径。观察到大肠杆菌FadR与ArcA-ArcB氧气反应性两组分系统之间的串扰,导致对某些fad regulonβ-氧化基因的调控。我们已经将这种分析扩展到了fadL和fadD基因,它们的蛋白质产物是长链脂肪酸运输所必需的,并且还研究了第三个全球调节因子CRP-cAMP复合物的作用。 fadL和fadD基因的启动子都包含两个经过实验验证的FadR结合位点以及ArcA和CRP-cAMP的结合位点。尽管存在双结合位点,但FadR仅适度调节这些基因的表达,表明结合位点的数目并不决定调节强度。我们报道了补充的体外和体内研究,表明CRP-cAMP复合物直接激活fadL和fadD以及β-氧化基因fadH的表达。 fadL和fadD转录数据的生理相关性通过长链脂肪酸转运的直接测定法得到验证。

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    Youjun Feng; John E. Cronan;

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  • 年(卷),期 -1(7),9
  • 年度 -1
  • 页码 e46275
  • 总页数 12
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