Enomoto Gen, Narikawa Rei, Ikeuchi Masahiko
Department of Life Sciences (Biology), Graduate School of Arts and Sciences, The University of Tokyo, Meguro, Tokyo 153-8902, Japan;
Department of Life Sciences (Biology), Graduate School of Arts and Sciences, The University of Tokyo, Meguro, Tokyo 153-8902, Japan; Department of Biological Science, Faculty of Science, Shizuoka University, Suruga-ku, Shizuoka 422-8529, Japan; Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012, Japan;
Proc Natl Acad Sci U S A. 2015 Jun 30;112(26):8082-7. doi: 10.1073/pnas.1504228112. Epub 2015 Jun 15.
Cyanobacteriochromes (CBCRs) are cyanobacterial photoreceptors that have diverse spectral properties and domain compositions. Although large numbers of CBCR genes exist in cyanobacterial genomes, no studies have assessed whether multiple CBCRs work together. We recently showed that the diguanylate cyclase (DGC) activity of the CBCR SesA from Thermosynechococcus elongatus is activated by blue-light irradiation and that, when irradiated, SesA, via its product cyclic dimeric GMP (c-di-GMP), induces aggregation of Thermosynechococcus vulcanus cells at a temperature that is suboptimum for single-cell viability. For this report, we first characterize the photobiochemical properties of two additional CBCRs, SesB and SesC. Blue/teal light-responsive SesB has only c-di-GMP phosphodiesterase (PDE) activity, which is up-regulated by teal light and GTP. Blue/green light-responsive SesC has DGC and PDE activities. Its DGC activity is enhanced by blue light, whereas its PDE activity is enhanced by green light. A ΔsesB mutant cannot suppress cell aggregation under teal-green light. A ΔsesC mutant shows a less sensitive cell-aggregation response to ambient light. ΔsesA/ΔsesB/ΔsesC shows partial cell aggregation, which is accompanied by the loss of color dependency, implying that a nonphotoresponsive DGC(s) producing c-di-GMP can also induce the aggregation. The results suggest that SesB enhances the light color dependency of cell aggregation by degrading c-di-GMP, is particularly effective under teal light, and, therefore, seems to counteract the induction of cell aggregation by SesA. In addition, SesC seems to improve signaling specificity as an auxiliary backup to SesA/SesB activities. The coordinated action of these three CBCRs highlights why so many different CBCRs exist.
蓝细菌色素(CBCRs)是蓝细菌中的光感受器,具有多样的光谱特性和结构域组成。尽管蓝细菌基因组中存在大量的CBCR基因,但尚无研究评估多个CBCR是否协同发挥作用。我们最近发现,来自嗜热栖热菌的CBCR SesA的二鸟苷酸环化酶(DGC)活性可被蓝光照射激活,并且在照射时,SesA通过其产物环二聚体鸟苷酸(c-di-GMP),在对单细胞生存力而言并非最适宜的温度下诱导嗜热栖热菌细胞聚集。在本报告中,我们首先对另外两种CBCR,即SesB和SesC的光生物化学特性进行了表征。对蓝/蓝绿色光有反应的SesB仅具有c-di-GMP磷酸二酯酶(PDE)活性,该活性可被蓝绿色光和GTP上调。对蓝/绿色光有反应的SesC具有DGC和PDE活性。其DGC活性被蓝光增强,而其PDE活性被绿光增强。ΔsesB突变体在蓝绿色光下不能抑制细胞聚集。ΔsesC突变体对环境光的细胞聚集反应较不敏感。ΔsesA/ΔsesB/ΔsesC显示出部分细胞聚集,同时伴随着颜色依赖性的丧失,这意味着产生c-di-GMP的非光响应性DGC也可诱导聚集。结果表明,SesB通过降解c-di-GMP增强了细胞聚集的光颜色依赖性,在蓝绿色光下尤为有效,因此似乎抵消了SesA对细胞聚集的诱导作用。此外,SesC似乎作为SesA/SesB活性的辅助备份提高了信号特异性。这三种CBCR的协同作用突出了为何存在如此多不同CBCR的原因。