Osterås M, Driscoll B T, Finan T M
Department of Biology, McMaster University, Hamilton, Ontario, Canada.
J Bacteriol. 1995 Mar;177(6):1452-60. doi: 10.1128/jb.177.6.1452-1460.1995.
The pckA gene of Rhizobium meliloti, encoding phosphoenolpyruvate carboxykinase, was isolated from a genomic cosmid library by complementation of the succinate growth phenotype of a Pck- mutant. The gene region was mapped by subcloning and Tn5 insertion mutagenesis. The DNA sequence for a 2-kb region containing the structural gene and its promoter was determined. The pckA gene encodes as 536-amino-acid protein that shows homology with other ATP-dependent Pck enzymes. The promoter was identified following primer extension analysis and is similar to sigma 70-like promoters. Expression analysis with a pckA::lacZ gene fusion indicated that the pckA gene was strongly induced at the onset of stationary phase in complex medium. When defined carbon sources were tested, the expression level of the pckA gene was found to be high when cells were grown in minimal media with succinate or arabinose as the sole carbon source but almost absent when glucose, sucrose, or glycerol was the sole carbon source. Glucose and sucrose were not found to strongly repress pckA induction by succinate.
通过对Pck-突变体琥珀酸生长表型的互补作用,从苜蓿根瘤菌的基因组黏粒文库中分离出编码磷酸烯醇式丙酮酸羧激酶的pckA基因。通过亚克隆和Tn5插入诱变对基因区域进行定位。测定了包含结构基因及其启动子的2 kb区域的DNA序列。pckA基因编码一种536个氨基酸的蛋白质,该蛋白质与其他ATP依赖性Pck酶具有同源性。通过引物延伸分析鉴定了启动子,其与σ70样启动子相似。用pckA::lacZ基因融合进行的表达分析表明,pckA基因在复合培养基中稳定期开始时被强烈诱导。当测试特定碳源时,发现当细胞在以琥珀酸或阿拉伯糖为唯一碳源的基本培养基中生长时,pckA基因的表达水平很高,但当葡萄糖、蔗糖或甘油为唯一碳源时,该基因几乎不表达。未发现葡萄糖和蔗糖强烈抑制琥珀酸对pckA的诱导作用。