Heatwole V M, Somerville R L
Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907.
J Bacteriol. 1991 Jun;173(11):3601-4. doi: 10.1128/jb.173.11.3601-3604.1991.
The regulation of transcription of the gene for the tryptophan-specific permease, mtr, was evaluated in several genetically marked Escherichia coli strains through the use of a single-copy lacZ reporter system. The expression of mtr was repressed 97-fold by tryptophan via the Trp repressor and induced 10-fold by phenylalanine or tyrosine via the Tyr repressor. By primer extension analysis two distinct mtr transcripts and their corresponding promoters were identified. One transcript was induced by the Tyr repressor. The tryptophan-dependent interaction of Trp repressor with an operator target within the mtr promoter was demonstrated by means of a restriction endonuclease protection assay.
通过使用单拷贝lacZ报告系统,在几种基因标记的大肠杆菌菌株中评估了色氨酸特异性通透酶基因mtr的转录调控。色氨酸通过色氨酸阻遏物使mtr的表达受到97倍的抑制,苯丙氨酸或酪氨酸通过酪氨酸阻遏物使mtr的表达诱导10倍。通过引物延伸分析鉴定出两种不同的mtr转录本及其相应的启动子。一种转录本由酪氨酸阻遏物诱导。通过限制性内切核酸酶保护试验证明了色氨酸阻遏物与mtr启动子内一个操纵子靶标的色氨酸依赖性相互作用。