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Identification and characterization of novel low-temperature-inducible promoters of Escherichia coli.

机译:大肠杆菌的新型低温诱导型启动子的鉴定和表征。

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摘要

Escherichia coli promoters that are more active at low temperature (15 to 20 degrees C) than at 37 degrees C were identified by using the transposon Tn5-lac to generate promoter fusions expressing beta-galactosidase (beta-Gal). Tn5-lac insertions that resulted in low-temperature-regulated beta-Gal expression were isolated by selecting kanamycin-resistant mutants capable of growth on lactose minimal medium at 15 degrees C but which grew poorly at 37 degrees C on this medium. Seven independent mutants were selected for further studies. In one such strain, designated WQ11, a temperature shift from 37 degrees C to either 20 or 15 degrees C resulted in a 15- to 24-fold induction of beta-Gal expression. Extended growth at 20 or 15 degrees C resulted in 36- to 42-fold-higher beta-Gal expression over that of cells grown at 37 degrees C. Treatment of WQ11 with streptomycin, reported to induce a response similar to heat shock, failed to induce beta-Gal expression. In contrast, treatment with either chloramphenicol or tetracycline, which mimics a cold shock response, resulted in a fourfold induction of beta-Gal expression in strain WQ11. Hfr genetic mapping studies complemented by physical mapping indicated that in at least three mutants (WQ3, WQ6, and WQ11), Tn5-lac insertions mapped at unique sites where no known cold shock genes have been reported. The Tn5-lac insertions of these mutants mapped to 81, 12, and 34 min on the E. coli chromosome, respectively. The cold-inducible promoters from two of the mutants (WQ3 and WQ11) were cloned and sequenced, and their temperature regulation was examined. Comparison of the nucleotide sequences of these two promoters with the regulatory elements of other known cold shock genes identified the sequence CCAAT as a putative conserved motif.
机译:通过使用转座子Tn5-lac生成表达β-半乳糖苷酶(β-Gal)的启动子融合蛋白,鉴定出在低温(15至20摄氏度)比37摄氏度下更具活性的大肠杆菌启动子。通过选择能够在15°C的乳糖基本培养基上生长但在37°C的条件下生长较差的卡那霉素抗性突变体,分离出导致低温调节的β-Gal表达的Tn5-lac插入。选择了七个独立的突变体用于进一步研究。在一种称为WQ11的此类菌株中,温度从37摄氏度转变为20摄氏度或15摄氏度会导致15到24倍的β-Gal表达诱导。与在37摄氏度下生长的细胞相比,在20摄氏度或15摄氏度下的长期生长导致β-Gal表达高36到42倍。用链霉素处理WQ11,据报道诱导了类似于热激的反应,但未能诱导β-Gal表达。相反,用氯霉素或四环素模拟冷休克反应,导致菌株WQ11中β-Gal表达的诱导达到四倍。 Hfr基因作图研究辅以物理作图表明,在至少三个突变体(WQ3,WQ6和WQ11)中,Tn5-lac插入位于未报道冷激基因报道的独特位点。这些突变体的Tn5-lac插入分别映射到大肠杆菌染色体上的81、12和34分钟。克隆并测序了来自两个突变体(WQ3和WQ11)的冷诱导型启动子,并检查了它们的温度调节。通过将这两个启动子的核苷酸序列与其他已知的冷休克基因的调控元件进行比较,确定了CCAAT序列为假定的保守基序。

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