Balas D, Fernández-Moreira E, De La Campa A G
Unidad de Genética Bacteriana (Consejo Superior de Investigaciones Científicas), Centro Nacional de Biología Fundamental, Instituto de Salud Carlos III, 28220 Majadahonda, Madrid, Spain.
J Bacteriol. 1998 Jun;180(11):2854-61. doi: 10.1128/JB.180.11.2854-2861.1998.
The gene encoding the DNA gyrase A subunit of Streptococcus pneumoniae was cloned and sequenced. The gyrA gene codes for a protein of 822 amino acids homologous to the gyrase A subunit of eubacteria. Translation of the gene in an Escherichia coli expression system revealed a 92-kDa polypeptide. A sequence-directed DNA curvature was identified in the promoter region of gyrA. The bend center was mapped and located between the -35 and -10 regions of the promoter. Primer extension analysis showed that gyrA transcription initiates 6 bp downstream of an extended -10 promoter. The possible implications of the bent DNA region as a regulatory element in the transcription of gyrA are discussed.
肺炎链球菌DNA促旋酶A亚基的编码基因被克隆并测序。gyrA基因编码一种由822个氨基酸组成的蛋白质,与真细菌的促旋酶A亚基同源。该基因在大肠杆菌表达系统中的翻译产生了一条92 kDa的多肽。在gyrA的启动子区域鉴定出了一个序列导向的DNA弯曲。弯曲中心被定位在启动子的-35区和-10区之间。引物延伸分析表明,gyrA转录起始于延伸的-10启动子下游6 bp处。讨论了弯曲DNA区域作为gyrA转录调控元件的可能意义。