Rogowsky P, Schmitt R
Mol Gen Genet. 1985;200(1):176-81. doi: 10.1007/BF00383332.
A 760 base pair nucleotide sequence of transposon Tn1721 containing the resolvase (tnpR) gene has been determined. A 186 triplet open reading frame was assigned to tnpR, and the allocation of -35 and -10 promoter boxes was supported by mapping transcription initiation at 70 base pairs upstream of tnpR. Expression of tnpR under tac promoter control generated sufficient resolvase protein for enzyme purification and for in vitro studies. Purified Tn1721 resolvase requires supercoiling and two directly oriented resolution (res) sites. The enzyme resolves cointegrate substrates containing repeat copies of Tn1721 res, of Tn21 res, of Tn21 res/Tn1721 res, but not of Tn3 res.
已确定包含解离酶(tnpR)基因的转座子Tn1721的一段760个碱基对的核苷酸序列。为tnpR指定了一个186个三联体的开放阅读框,通过在tnpR上游70个碱基对处定位转录起始,支持了-35和-10启动子框的定位。在tac启动子控制下tnpR的表达产生了足够的解离酶蛋白,用于酶的纯化和体外研究。纯化的Tn1721解离酶需要超螺旋和两个直接定向的解离(res)位点。该酶可解离含有Tn1721 res、Tn21 res、Tn21 res/Tn1721 res重复拷贝的共整合底物,但不能解离Tn3 res的底物。