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大肠杆菌新型低温诱导型启动子的鉴定与表征

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

作者信息

Qoronfleh M W, Debouck C, Keller J

机构信息

Department of Biological Process Sciences, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406.

出版信息

J Bacteriol. 1992 Dec;174(24):7902-9. doi: 10.1128/jb.174.24.7902-7909.1992.

Abstract

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.

摘要

通过使用转座子Tn5-lac来产生表达β-半乳糖苷酶(β-Gal)的启动子融合体,鉴定出了在低温(15至20摄氏度)下比在37摄氏度时更具活性的大肠杆菌启动子。通过选择能够在15摄氏度的乳糖基本培养基上生长但在37摄氏度时在此培养基上生长不良的卡那霉素抗性突变体,分离出导致低温调节β-Gal表达的Tn5-lac插入片段。选择了七个独立的突变体进行进一步研究。在一个这样的菌株中,命名为WQ11,温度从37摄氏度转变为20或15摄氏度会导致β-Gal表达诱导15至24倍。在20或15摄氏度下长时间生长导致β-Gal表达比在37摄氏度下生长的细胞高36至42倍。用据报道可诱导类似于热休克反应的链霉素处理WQ11,未能诱导β-Gal表达。相反,用模拟冷休克反应的氯霉素或四环素处理,导致菌株WQ11中β-Gal表达诱导四倍。通过物理图谱补充的高频重组(Hfr)遗传图谱研究表明,在至少三个突变体(WQ3、WQ6和WQ11)中,Tn5-lac插入位于尚未报道已知冷休克基因的独特位点。这些突变体的Tn5-lac插入分别定位在大肠杆菌染色体上的81、12和34分钟处。克隆并测序了两个突变体(WQ3和WQ11)的冷诱导启动子,并检查了它们的温度调节。将这两个启动子的核苷酸序列与其他已知冷休克基因的调控元件进行比较,确定序列CCAAT为假定的保守基序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa28/207524/6ff2239c5e3d/jbacter00090-0033-a.jpg

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