Eccles S J, Chopra I
J Bacteriol. 1984 Apr;158(1):134-40. doi: 10.1128/jb.158.1.134-140.1984.
A fragment of Bacillus plasmid pAB124 carrying the genes encoding tetracycline resistance was previously cloned into Escherichia coli plasmid pSF2124 (S.J. Eccles, A. Docherty, I. Chopra, S. Shales, and P. Ball, J. Bacteriol. 145:1417-1420, 1981). The cloned pAB124 tet fragment conferred low-level resistance in E. coli, but exposure of this strain to a subinhibitory level of tetracycline led to selection of a mutant plasmid in which high-level resistance, associated with decreased drug accumulation, was expressed constitutively. In this plasmid, the Bacillus tet determinant appeared to be transcribed from a promoter on the vector. Construction of tetracycline-sensitive derivatives of this plasmid by transposon insertion mutagenesis allowed identification of a 32,000-dalton membrane-located protein, which apparently promoted decreased accumulation of tetracycline. This protein was also synthesized as a 32,000-dalton polypeptide in a coupled, in vitro transcription-translation system directed by plasmid DNA. The pAB124 tet determinant differed from the tetA through tetD determinants found in gram-negative bacteria in DNA-DNA hybridization and in the ability to prevent accumulation of different tetracycline derivatives, but was closely related to the tet determinant of another plasmid isolated from Bacillus species, pBC16.
携带编码四环素抗性基因的芽孢杆菌质粒pAB124的一个片段先前已被克隆到大肠杆菌质粒pSF2124中(S.J.埃克尔斯、A.多彻蒂、I.乔普拉、S.沙尔斯和P.鲍尔,《细菌学杂志》145:1417 - 1420,1981年)。克隆的pAB124四环素片段在大肠杆菌中赋予低水平抗性,但将该菌株暴露于亚抑制水平的四环素会导致选择出一种突变质粒,其中高水平抗性与药物积累减少相关,且这种抗性是组成型表达的。在该质粒中,芽孢杆菌四环素决定簇似乎是从载体上的一个启动子转录而来的。通过转座子插入诱变构建该质粒的四环素敏感衍生物,使得能够鉴定出一种32000道尔顿的膜定位蛋白,该蛋白显然促进了四环素积累的减少。在由质粒DNA指导的体外偶联转录 - 翻译系统中,这种蛋白也作为一种32000道尔顿的多肽被合成。在DNA - DNA杂交以及防止不同四环素衍生物积累的能力方面,pAB124四环素决定簇与在革兰氏阴性菌中发现的tetA至tetD决定簇不同,但与从芽孢杆菌属分离的另一个质粒pBC16的四环素决定簇密切相关。