Tabei Yosuke, Okada Katsuhiko, Tsuzuki Mikio
School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Horinouchi, Hachioji, Tokyo 192-0392, Japan.
Biochem Biophys Res Commun. 2007 Apr 20;355(4):1045-50. doi: 10.1016/j.bbrc.2007.02.065. Epub 2007 Feb 22.
In the complete annotated genome sequences of cyanobacterium Synechocystis sp. PCC 6803, one can find many putative genes for two-component response regulators that include a helix-turn-helix DNA-binding domain. The mRNA level of one of the putative genes, sll1330, was increased by glucose, especially in the presence of light. We successfully disrupted the sll1330 gene by targeted mutagenesis with a spectinomycin resistance cassette. Deltasll1330 could not grow well under light-activated heterotrophic growth conditions. Analyses of the expression of glycolytic genes revealed that the mRNA levels of five glycolytic genes, that is, glk (sll0593), pfkA (sll1196), fbaA (sll0018), gpmB (slr1124), and pk (sll0587), were decreased, and were regulated by Sll1330 under light and glucose-supplemented conditions. The Synechocystis sp. PCC 6803 genome each encodes two isozymes for these five glycolytic genes, suggesting that each of the two isozymes is regulated by Sll1330 at the mRNA level.
在集胞藻6803(Synechocystis sp. PCC 6803)的完整注释基因组序列中,可以找到许多假定的双组分响应调节因子基因,这些基因包含一个螺旋-转角-螺旋DNA结合结构域。其中一个假定基因sll1330的mRNA水平在葡萄糖存在下会升高,尤其是在光照条件下。我们通过用壮观霉素抗性盒进行定点诱变成功破坏了sll1330基因。缺失sll1330的突变体在光激活的异养生长条件下生长不佳。糖酵解基因表达分析表明,在光照和补充葡萄糖的条件下,五个糖酵解基因,即glk(sll0593)、pfkA(sll1196)、fbaA(sll0018)、gpmB(slr1124)和pk(sll0587)的mRNA水平降低,且受Sll1330调控。集胞藻6803基因组为这五个糖酵解基因各编码两种同工酶,这表明两种同工酶在mRNA水平上均受Sll1330调控。