Kaczorek M, Zettlmeissl G, Delpeyroux F, Streeck R E
Nucleic Acids Res. 1985 May 10;13(9):3147-59. doi: 10.1093/nar/13.9.3147.
The expression of the diphtheria tox228 gene encoding the nontoxic, serologically related CRM228 mutant diphtheria toxin has been analyzed in Corynebacterium diphtheriae and Escherichia coli. The diphtheria toxin promoter has been used to direct the expression of beta-galactosidase in E.coli, and the efficiency of promotion has been compared to that obtained with the lac promoter. Expression in C.diphtheriae is known to be dependent on the absence of iron, and we present for the first time direct evidence that this regulation occurs at the level of transcription. The 5' end of toxin mRNA maps at the same position in C.diphtheriae and E.coli, suggesting identical sequences to be recognized by C.diphtheriae and E.coli RNA polymerase. The diphtheria toxin promoter carries at position -34 a TTGATT sequence closely related to the E.coli -35 consensus sequence and in the -14 to -8 region a set of overlapping sequences with complete or partial homology to the E.coli -10 consensus sequence.
对编码无毒、血清学相关CRM228突变型白喉毒素的白喉毒素tox228基因在白喉棒状杆菌和大肠杆菌中的表达进行了分析。白喉毒素启动子已被用于指导β-半乳糖苷酶在大肠杆菌中的表达,并将其促进效率与乳糖启动子获得的效率进行了比较。已知白喉棒状杆菌中的表达依赖于铁的缺失,我们首次提供了直接证据表明这种调控发生在转录水平。毒素mRNA的5'端在白喉棒状杆菌和大肠杆菌中的定位相同,这表明白喉棒状杆菌和大肠杆菌RNA聚合酶识别相同的序列。白喉毒素启动子在-34位带有一个与大肠杆菌-35共有序列密切相关的TTGATT序列,在-14至-8区域有一组与大肠杆菌-10共有序列完全或部分同源的重叠序列。