作者: C F Beck , R Mutzel , J Barbé , W Müller
DOI: 10.1128/JB.150.2.633-642.1982
关键词:
摘要: The tetracycline resistance regulatory gene (tetR) of transposon Tn10 was analyzed by a combination methods involving fusion and cloning. This is located on 695-base pair HincII DNA fragment near the center Tn10. direction transcription opposite to that neighboring tetA, which encodes TetA protein. product tetR (the TetR protein) has molecular weight 23,000. tet-R-lacZ fusions encode beta-galactosidases are membrane bound, indicating protein itself associated. Mutants defective in result constitutive resistance, but level reduced. Expression induced tetracycline; absence tetracycline, turns off its own synthesis.