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Cloning, nucleotide sequence, and characterization of mtr, the structural gene for a tryptophan-specific permease of Escherichia coli K-12.

机译:克隆,核苷酸序列和mtr的表征,mtr是大肠杆菌K-12色氨酸特异性渗透酶的结构基因。

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摘要

The mtr gene of Escherichia coli K-12 encodes an L-tryptophan-specific permease. This gene was originally identified through the isolation of mutations in the 69-min region of the chromosome, closely linked to argG. Cells with lesions in mtr display a phenotype of 5-methyltryptophan resistance. The mtr gene was cloned by using the mini-Mu system. The amino acid sequence of Mtr (414 codons), deduced by DNA sequence analysis, was found to be 33% identical to that of another single-component transport protein, the tyrosine-specific permease, TyrP. The hydropathy plots of the two permeases were similar. Possible operator sites for the tyrosine and tryptophan repressors are situated within the region of DNA that is likely to be the mtr promoter.
机译:大肠杆菌K-12的mtr基因编码L-色氨酸特异性通透酶。该基因最初是通过分离染色体上69分钟区域中与argG紧密相关的突变而鉴定的。在mtr中具有损伤的细胞表现出5-甲基色氨酸抗性的表型。使用mini-Mu系统克隆了mtr基因。通过DNA序列分析推导的Mtr(414个密码子)的氨基酸序列与另一种单组分转运蛋白酪氨酸特异性通透酶TyrP具有33%的同源性。两种通透酶的亲水性图相似。酪氨酸和色氨酸阻遏物的可能的操纵位点位于可能是mtr启动子的DNA区域内。

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