Lozinski T, Markiewicz W T, Wyrzykiewicz T K, Wierzchowski K L
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa.
Nucleic Acids Res. 1989 May 25;17(10):3855-63. doi: 10.1093/nar/17.10.3855.
Three E.coli promoters with the consensus sequences in the -35 and -10 regions and the 17 bp spacer made of random, heteronomous, and of both these classes of AT DNA simultaneously were constructed and cloned into plasmid pDS3. Electrophoretic gel mobilities of restriction fragments containing these promoters indicated that bending of the latter was proportional to the number of heteronomous AT DNA tracts. The strength of these promoters in vivo measured in relation to an internal transcriptional standard was shown to correlate well with gel mobilities of the respective restriction fragments and to decrease with the number of potential DNA bending sites encoded in the promoter structure.
构建了三个大肠杆菌启动子,它们在-35和-10区域具有共有序列,并且其17bp间隔区同时由随机、异源以及这两类AT DNA组成,随后将其克隆到质粒pDS3中。含有这些启动子的限制性片段的电泳凝胶迁移率表明,后者的弯曲程度与异源AT DNA片段的数量成正比。相对于内部转录标准在体内测量的这些启动子的强度,与相应限制性片段的凝胶迁移率高度相关,并且随着启动子结构中编码的潜在DNA弯曲位点数量的增加而降低。