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Regulation of fatty acid degradation in Escherichia coli: fadR superrepressor mutants are unable to utilize fatty acids as the sole carbon source.

机译:大肠杆菌中脂肪酸降解的调控:fadR超阻遏物突变体无法利用脂肪酸作为唯一碳源。

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摘要

Localized mutagenesis of the fadR region of the Escherichia coli chromosome resulted in the isolation of two classes of fadR regulatory mutants. The first class was constitutive for the fatty acid degradative enzymes and presumably defective for fadR function. The second class was rarer and resulted in the inability to utilize fatty acids as a sole carbon source (Fad-). These fadR superrepressor mutants [fadR(S)] had greatly reduced levels of the beta-oxidative enzymes required for growth on fatty acids. The fadR(S) mutants reverted to Fad+ at a high frequency (10(-5], and the resulting Fad+ revertants were constitutive for expression of the fad enzymes (fadR). Merodiploid analysis showed the fadR(S) allele to be dominant to both fadR+ and fadR alleles.
机译:大肠杆菌染色体的fadR区的局部诱变导致分离出两类fadR调节突变体。第一类是脂肪酸降解酶的组成成分,可能是fadR功能的缺陷。第二类较为罕见,导致无法利用脂肪酸作为唯一碳源(Fad-)。这些fadR超阻遏突变体[fadR(S)]大大降低了在脂肪酸上生长所需的β-氧化酶的水平。 fadR(S)突变体以高频率还原为Fad +(10(-5),所得的Fad +回复子是fad酶(fadR)表达的组成成分。倍二倍体分析显示fadR(S)等位基因占优势fadR +和fadR等位基因。

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