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Cloning and nucleotide sequence of the leucyl-tRNA synthetase gene of Bacillus subtilis.

机译:枯草芽孢杆菌亮氨酰tRNA合成酶基因的克隆及核苷酸序列。

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摘要

The leucyl-tRNA synthetase gene (leuS) of Bacillus subtilis was cloned and sequenced. A mutation in the gene, leuS1, increases the transcription and expression of the ilv-leu operion, permitting monitoring of leuS alleles. The leuS1 mutation was mapped to 270 degrees on the chromosome. Sequence analysis showed that the mutation is a single-base substitution, possibly in a monocistronic operon. The leader mRNA predicted by the sequence would contain a number of possible secondary structures and a T box, a sequence observed upstream of leader mRNA terminators of Bacillus tRNA synthetases and the B. subtilis ilv-leu operon. The DNA of the B. subtilis leuS open reading frame is 48% identical to the leuS gene of Escherichia coli and is predicted to encode a polypeptide with 46% identity to the leucyl-tRNA synthetase of E. coli.
机译:枯草芽孢杆菌的亮氨酰tRNA合成酶基因(leuS)被克隆并测序。基因leuS1中的突变增加了ilv-leu操纵子的转录和表达,从而可以监测leuS等位基因。 leuS1突变在染色体上定位为270度。序列分析表明该突变是单碱基取代,可能在单顺反子操纵子中。由该序列预测的前导mRNA将包含许多可能的二级结构和一个T盒,即在芽孢杆菌tRNA合成酶和枯草芽孢杆菌ilv-leu操纵子的前导mRNA终止子上游观察到的序列。枯草芽孢杆菌leuS开放阅读框的DNA与大肠杆菌的leuS基因具有48%的同一性,并被预测为编码与大肠杆菌的亮氨酰tRNA合成酶具有46%的同一性的多肽。

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