Hamann A, Bossemeyer D, Bakker E P
J Bacteriol. 1987 Jul;169(7):3138-45. doi: 10.1128/jb.169.7.3138-3145.1987.
The position on the Escherichia coli chromosome of trkA, a gene coding for a membrane protein involved in K+ transport by the constitutive uptake system Trk, was determined. We observed that the gene is transcribed in a clockwise direction and that it is located at 72.4 min on the chromosome in a 1.75-kilobase NruI-EcoRV DNA fragment 1.0 kilobase upstream of rplQ. We localized an additional gene encoding a 17,000-molecular-weight protein of unknown function between the trkA and rplQ genes. A plasmid, pDB3, was constructed in which the transcription of the trkA gene was put under the control of the lambda pL promoter. pDB3-containing cells of a strain, which contained the temperature-sensitive lambda repressor cI857 in the chromosome, overproduced the 53,000-molecular-weight TrkA protein at the nonpermissive temperature to such an extent that TrkA became the major cell protein. From cell fractionation studies, we conclude that the overproduced TrkA protein forms aggregates.
确定了trkA基因在大肠杆菌染色体上的位置,该基因编码一种参与组成型摄取系统Trk进行钾离子转运的膜蛋白。我们观察到该基因按顺时针方向转录,位于染色体上72.4分钟处,在rplQ上游1.0千碱基的1.75千碱基NruI - EcoRV DNA片段中。我们在trkA和rplQ基因之间定位了另一个编码功能未知的17,000分子量蛋白质的基因。构建了一个质粒pDB3,其中trkA基因的转录置于λ pL启动子的控制之下。在染色体中含有温度敏感型λ阻遏物cI857的菌株中,含pDB3的细胞在非允许温度下过量产生53,000分子量的TrkA蛋白,以至于TrkA成为主要的细胞蛋白。通过细胞分级分离研究,我们得出结论,过量产生的TrkA蛋白形成聚集体。