Osanai Takashi, Kanesaki Yu, Nakano Takayuki, Takahashi Hiroyuki, Asayama Munehiko, Shirai Makoto, Kanehisa Minoru, Suzuki Iwane, Murata Norio, Tanaka Kan
Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
J Biol Chem. 2005 Sep 2;280(35):30653-9. doi: 10.1074/jbc.M505043200. Epub 2005 Jun 8.
The sigE gene of Synechocystis sp. PCC 6803 encodes a group 2 sigma factor for RNA polymerase and has been proposed to function in transcriptional regulation of nitrogen metabolism. By using microarray and Northern analyses, we demonstrated that the abundance of transcripts derived from genes important for glycolysis, the oxidative pentose phosphate pathway, and glycogen catabolism is reduced in a sigE mutant of Synechocystis maintained under the normal growth condition. Furthermore, the activities of the two key enzymes of the oxidative pentose phosphate pathway, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase, encoded by the zwf and gnd genes were also reduced in the sigE mutant. The dark enhancements in both enzyme activity and transcript abundance apparent in the wild type were eliminated by the mutation. In addition, the sigE mutant showed a reduced rate of glucose uptake and an increased intracellular level of glycogen. Moreover, it was unable to proliferate under the light-activated heterotrophic growth conditions. These results indicate that SigE functions in the transcriptional activation of sugar catabolic pathways in Synechocystis sp. PCC 6803.
集胞藻6803(Synechocystis sp. PCC 6803)的sigE基因编码一种RNA聚合酶的2类σ因子,有人提出它在氮代谢的转录调控中发挥作用。通过使用微阵列和Northern分析,我们证明,在正常生长条件下培养的集胞藻sigE突变体中,源自对糖酵解、氧化戊糖磷酸途径和糖原分解重要的基因的转录本丰度降低。此外,由zwf和gnd基因编码的氧化戊糖磷酸途径的两种关键酶,即葡萄糖-6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶的活性,在sigE突变体中也降低。野生型中明显的酶活性和转录本丰度的暗增强被该突变消除。此外,sigE突变体显示出葡萄糖摄取速率降低和细胞内糖原水平升高。此外,它在光激活的异养生长条件下无法增殖。这些结果表明,SigE在集胞藻6803糖分解代谢途径的转录激活中发挥作用。