McLaughlin J R, Chang S Y, Chang S
Nucleic Acids Res. 1982 Jul 10;10(13):3905-19. doi: 10.1093/nar/10.13.3905.
We report the promoter structure of the Bacillus licheniformis 749/C penicillinase (penP) gene. The transcript encoding the penicillinase gene was identified by in vitro run-off transcription using both E. coli RNA polymerase and B. subtilis RNA polymerase. Utilization of this promoter in linearized DNA by the B. subtilis RNA polymerase showed extreme sensitivity to ionic strength. The 5' sequence of the penP mRNA was determined using enzymatic sequencing (1). Holoenzymes from E. coli and B. subtilis (E sigma 55) initiate penP RNA synthesis at the same site. Alignment of this RNA sequence with the reported DNA sequence of ther penP gene (2,3) revealed the "-35 region" and "Pribnow box" sequences that are recognized as 5'TTGCAT and 5'AATACT, respectively. Potential secondary structure within the promoter exists which may play a role in the expression of the penicillinase gene. The location of the penP promoter was further confirmed by molecular cloning of a DNA fragment containing the expected promoter sequence into a promoter-fishing vector useful for monitoring promoter activities in both E. coli and B. subtilis.
我们报道了地衣芽孢杆菌749/C青霉素酶(penP)基因的启动子结构。通过使用大肠杆菌RNA聚合酶和枯草芽孢杆菌RNA聚合酶进行体外径流转录,鉴定了编码青霉素酶基因的转录本。枯草芽孢杆菌RNA聚合酶在线性化DNA中对该启动子的利用显示出对离子强度的极端敏感性。使用酶促测序法确定了penP mRNA的5'序列(1)。来自大肠杆菌和枯草芽孢杆菌的全酶(E sigma 55)在同一位置起始penP RNA合成。将该RNA序列与已报道的penP基因DNA序列(2,3)进行比对,发现分别被识别为5'TTGCAT和5'AATACT的“-35区”和“Pribnow框”序列。启动子内存在潜在的二级结构,其可能在青霉素酶基因的表达中发挥作用。通过将包含预期启动子序列的DNA片段分子克隆到一个可用于监测大肠杆菌和枯草芽孢杆菌中启动子活性的启动子捕获载体中,进一步证实了penP启动子的位置。