Tsunedomi Ryouichi, Izu Hanae, Kawai Takuya, Yamada Mamoru
Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, Yamaguchi, Japan.
J Mol Microbiol Biotechnol. 2003;6(1):41-56. doi: 10.1159/000073407.
Escherichia coli possesses two systems, GntI and GntII, for gluconate uptake and catabolism, whose genes are regulated by GntR as a repressor and GntH as an activator, respectively. Additionally, GntH exerts negative control of the GntI genes via the same binding element as that of GntR. We thus examined whether GntR involves regulation of the GntII genes or not. This regulation and the control by GntH were examined by using single-copy LACZ operon fusions and by RT-PCR, suggesting positive and negative regulation by GntR and positive regulation by GntH. Moreover, the introduction of mutations into possible GntR-binding elements revealed that both regulators share at least one of the elements. The results presented allow us to speculate that GntR initiates expression of the GntII genes, followed by their large induction by GntH when cells were grown in gluconate minimum medium. As in the case of the GntI genes, such a cross-regulation between the GntI and GntII via the two regulators may be important for cells to grow with gluconate.
大肠杆菌拥有两套用于摄取和分解葡萄糖酸盐的系统,即GntI和GntII,其基因分别受作为阻遏物的GntR和作为激活物的GntH调控。此外,GntH通过与GntR相同的结合元件对GntI基因进行负调控。因此,我们研究了GntR是否参与GntII基因的调控。通过使用单拷贝LACZ操纵子融合和RT-PCR研究了这种调控以及GntH的控制作用,结果表明GntR存在正调控和负调控,而GntH存在正调控。此外,对可能的GntR结合元件引入突变后发现,这两种调节因子至少共享其中一个元件。本文给出的结果使我们推测,当细胞在葡萄糖酸盐基本培养基中生长时,GntR启动GntII基因的表达,随后由GntH对其进行大量诱导。与GntI基因的情况一样,通过这两种调节因子在GntI和GntII之间进行的这种交叉调控对于细胞利用葡萄糖酸盐生长可能很重要。