首页> 美国卫生研究院文献>Journal of Bacteriology >Thiolactomycin resistance in Escherichia coli is associated with the multidrug resistance efflux pump encoded by emrAB.
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Thiolactomycin resistance in Escherichia coli is associated with the multidrug resistance efflux pump encoded by emrAB.

机译:大肠埃希菌中的丝裂霉素耐药性与emrAB编码的多药耐药性外排泵有关。

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摘要

Thiolactomycin (TLM) and cerulenin are antibiotics that block Escherichia coli growth by inhibiting fatty acid biosynthesis at the beta-ketoacyl-acyl carrier protein synthase I step. Both TLM and cerulenin trigger the accumulation of intracellular malonyl-coenzyme A coincident with growth inhibition, and the overexpression of synthase I protein confers resistance to both antibiotics. Strain CDM5 was derived as a TLM-resistant mutant but remained sensitive to cerulenin. TLM neither induced malonyl-coenzyme A accumulation nor blocked fatty acid production in vivo; however, the fatty acid synthase activity in extracts from strain CDM5 was sensitive to TLM inhibition. The TLM resistance gene in strain CDM5 was mapped to 57.5 min of the chromosome and was an allele of the emrB gene. Disruption of the emrB gene converted strain CDM5 to a TLM-sensitive strain, and the overexpression of the emrAB operon conferred TLM resistance to sensitive strains. Thus, activation of the emr efflux pump is the mechanism for TLM resistance in strain CDM5.
机译:硫菌霉素(TLM)和铜绿素是通过在β-酮酰基-酰基载体蛋白合酶I步骤抑制脂肪酸生物合成来阻止大肠杆菌生长的抗生素。 TLM和铜蓝蛋白都触发了细胞内丙二酸辅酶A的积累,同时抑制了生长,并且合酶I蛋白的过表达赋予了对两种抗生素的抗性。菌株CDM5衍生为TLM抗性突变体,但对铜蓝蛋白仍然敏感。 TLM既不诱导丙二酰辅酶A的积累,也没有阻断体内脂肪酸的产生。但是,菌株CDM5提取物中的脂肪酸合酶活性对TLM抑制敏感。菌株CDM5中的TLM抗性基因定位在染色体的57.5分钟处,并且是emrB基因的等位基因。 emrB基因的破坏将菌株CDM5转化为TLM敏感菌株,而emrAB操纵子的过表达使TLM对敏感菌株产生抗性。因此,emr外排泵的激活是菌株CDM5中TLM抗性的机制。

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