Tovar K, Ernst A, Hillen W
Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Federal Republic of Germany.
Mol Gen Genet. 1988 Dec;215(1):76-80. doi: 10.1007/BF00331306.
The regulatory region and repressor (tetRE) gene from the class E tetracycline resistance determinant previously isolated from Enterobacteriaceae have been identified and completely sequenced. The regulatory region is located between the resistance gene and the tetR gene which have opposite polarity. The tetR gene encodes a protein consisting of 211 amino acids with a calculated molecular weight of 23.6 kDa. Cloning of the tetR gene under transcriptional control of the lambda PL promoter leads to overexpression of a polypeptide with an apparent molecular weight of 26 kDa. The purified protein binds sequence specifically to DNA fragments containing putative tet operators. This property is lost in the presence of tetracycline. The relationship of the tetRE sequence to four known tetracycline resistance determinants is discussed.
先前从肠杆菌科分离出的E类四环素抗性决定簇的调控区和阻遏物(tetRE)基因已被鉴定并完成测序。调控区位于抗性基因和极性相反的tetR基因之间。tetR基因编码一种由211个氨基酸组成的蛋白质,计算分子量为23.6 kDa。在λPL启动子的转录控制下克隆tetR基因会导致表观分子量为26 kDa的多肽过表达。纯化的蛋白质与含有假定tet操纵子的DNA片段特异性结合。在四环素存在的情况下,这种特性会丧失。讨论了tetRE序列与四个已知四环素抗性决定簇的关系。