Yamamoto Kaneyoshi, Nakano Masahiro, Ishihama Akira
Research Institute of Micro-Nano Technology, Hosei University, Koganei, Tokyo 185-8584, Japan.
Department of Frontier Bioscience, Hosei University, Koganei, Tokyo 185-8584, Japan.
Microbiology (Reading). 2015 Jan;161(Pt 1):99-111. doi: 10.1099/mic.0.083550-0. Epub 2014 Nov 18.
Sulfur makes up 1 % of the dry mass of bacteria, and it is an abundant element (0.1 %) on earth. Sulfur in the environment is, however, mostly in oxidized forms and inaccessible to living organisms. At present, the entire assimilation pathway of external sulfur to sulfur-containing biomolecules and its regulation in Escherichia coli remain poorly understood, except for the metabolic pathway of cysteine synthesis, the first-step metabolite of sulfur assembly. During the search for regulation targets of uncharacterized transcription factors by Genomic SELEX screening, we found that the hitherto uncharacterized YdcN regulates a set of genes involved in the utilization of sulfur, including the generation of sulfate and its reduction, the synthesis of cysteine, the synthesis of enzymes containing Fe-S as cofactors, and the modification of tRNA with use of sulfur-containing substrates. Taking these findings together, we propose renaming YdcN as SutR (regulator of sulfur utilization).
硫占细菌干重的1%,是地球上一种丰富的元素(0.1%)。然而,环境中的硫大多以氧化形式存在,生物体无法利用。目前,除了硫组装的第一步代谢产物半胱氨酸合成的代谢途径外,外界硫到含硫生物分子的整个同化途径及其在大肠杆菌中的调控仍知之甚少。在通过基因组SELEX筛选寻找未表征转录因子的调控靶点的过程中,我们发现迄今为止未表征的YdcN调控一组参与硫利用的基因,包括硫酸盐的产生及其还原、半胱氨酸的合成、含Fe-S作为辅因子的酶的合成以及利用含硫底物对tRNA的修饰。综合这些发现,我们建议将YdcN重新命名为SutR(硫利用调节因子)。