Francoz E, Dassa E
Unité de Programmation Moléculaire et de Toxicologie Génétique, CNRS UA271, INSERM U163, Institut Pasteur, Paris, France.
Nucleic Acids Res. 1988 May 11;16(9):4097-109. doi: 10.1093/nar/16.9.4097.
The nucleotide sequence of a 981 bp's HincII-PvuII DNA fragment containing the 3' end of the malEFG operon in E. coli was determined. This sequence displayed a putative Rho-independent transcription termination site localized 87 bp's after the stop codon of malG. When cloned into plasmid pKG1800, the HincII-PvuII fragment containing this structure acted as a strong transcription termination signal. By S1 mapping, we demonstrated that the 3' end of the malEFG transcript coincided with the putative transcription termination site. One short open reading frames orf1 (123 bp) and and the beginning of another one orf2 were localized after malG. The transcription termination site is localized within orf1. Consequently malG is the last gene of the malEFG operon. orf2 corresponds exactly to the 5' part of the xylE gene reported independently (Davis & Henderson, 1987) as the gene coding for the XylE protein, the xylose-proton symport of Escherichia coli.
测定了大肠杆菌中包含malEFG操纵子3'端的一段981 bp的HincII - PvuII DNA片段的核苷酸序列。该序列显示在malG的终止密码子后87 bp处有一个假定的不依赖Rho的转录终止位点。当克隆到质粒pKG1800中时,含有该结构的HincII - PvuII片段作为一个强转录终止信号。通过S1作图,我们证明了malEFG转录本的3'端与假定的转录终止位点一致。在malG之后定位了一个短的开放阅读框orf1(123 bp)和另一个orf2的起始部分。转录终止位点位于orf1内。因此,malG是malEFG操纵子的最后一个基因。orf2恰好对应于独立报道的(Davis & Henderson,1987)作为编码XylE蛋白(大肠杆菌的木糖 - 质子同向转运体)的基因的xylE基因的5'部分。