Leiting B, Noegel A A
Max-Planck-Institut für Biochemie, Martinsried bei München, F.R.G.
Biochem Biophys Res Commun. 1991 Nov 14;180(3):1403-7. doi: 10.1016/s0006-291x(05)81352-x.
An expression cassette has been constructed which allows expression of the ble gene isolated from Streptoalloteichus hindustanus in Dictyostelium discoideum. This construct has been shown to confer resistance to the bleomycin related antibiotic phleomycin. since the uptake of phleomycin by the cells is pH dependent, we established conditions that allow selection of phleomycin-resistant transformants. Vectors pfeI and pfeII contain, in addition to the cassette, a 592 bp fragment of the D. discoideum plasmid Ddp2 that enables the plasmids to replicate extrachromosomally in Dictyostelium when transformed into a strain that expresses a Ddp2-specific transacting factor (12). pfeI and pfeII contain various unique restriction enzyme sites for cloning. They differ in the G/C-content of the sequence upstream of the ATG start codon.
构建了一个表达盒,其可使从印度斯坦链霉菌分离的ble基因在盘基网柄菌中表达。已证明该构建体能赋予对博来霉素相关抗生素腐草霉素的抗性。由于细胞对腐草霉素的摄取依赖于pH,我们建立了允许选择腐草霉素抗性转化体的条件。载体pfeI和pfeII除了该表达盒外,还含有盘基网柄菌质粒Ddp2的一个592 bp片段,当转化到表达Ddp2特异性反式作用因子的菌株中时,该片段能使质粒在盘基网柄菌中进行染色体外复制(12)。pfeI和pfeII含有各种用于克隆的独特限制性酶切位点。它们在ATG起始密码子上游序列的G/C含量上有所不同。