Milner J L, Wood J M
Department of Chemistry and Biochemistry, University of Guelph, Ontario, Canada.
J Bacteriol. 1989 Feb;171(2):947-51. doi: 10.1128/jb.171.2.947-951.1989.
Mutation pro-220::Tn5, which increases the resistance of Escherichia coli to 3,4-dehydroproline (M. E. Stalmach, S. Grothe, and J. M. Wood, J. Bacteriol. 156:481-486, 1983), is not linked to putP, proP, or proU. It was located at 40.4 min on the E. coli chromosomal linkage map, by conjugational and transductional mapping, and is now denoted proQ220::Tn5. Proline porter II was not detectable when proQ220::Tn5 proP+ bacteria were cultivated under optimal conditions or with nutritional stress (amino acid limitation). Toxic proline analog sensitivity and proline porter II activity were partially restored to proQ220::Tn5 proP+ bacteria, but not to a proQ220::Tn5 proP219 strain, by a hyperosmotic shift and by growth under osmotic stress. Elevated expression of a proP::lacZ gene fusion, for bacteria grown under osmotic stress, was not influenced by the proQ220::Tn5 insertion. We propose that the proQ locus encodes a positive regulatory element which elevates proline porter II activity.
pro - 220::Tn5突变可增加大肠杆菌对3,4 - 脱氢脯氨酸的抗性(M. E. 斯塔尔马赫、S. 格罗特和J. M. 伍德,《细菌学杂志》156:481 - 486,1983年),它与putP、proP或proU不连锁。通过接合和转导作图,它位于大肠杆菌染色体连锁图谱的40.4分钟处,现在被命名为proQ220::Tn5。当proQ220::Tn5 proP⁺细菌在最佳条件下或在营养应激(氨基酸限制)下培养时,脯氨酸转运蛋白II无法检测到。通过高渗转变和在渗透应激下生长,proQ220::Tn5 proP⁺细菌的有毒脯氨酸类似物敏感性和脯氨酸转运蛋白II活性部分恢复,但proQ220::Tn5 proP219菌株未恢复。对于在渗透应激下生长的细菌,proP::lacZ基因融合的表达升高不受proQ220::Tn5插入的影响。我们提出proQ基因座编码一种正调控元件,可提高脯氨酸转运蛋白II的活性。