Department of Bacteriology, Graduate School of Medicine, Nagoya, Japan.
FEMS Microbiol Lett. 2009 Dec;301(2):193-200. doi: 10.1111/j.1574-6968.2009.01825.x.
Cyclic bis(3'-5')diguanylic acid (cyclic-di-GMP) functions as a second messenger in diverse species of bacteria to trigger wide-ranging physiological changes. We measured cyclic-di-GMP and its structural analogs such as cyclic bis(3'-5')guanylic/adenylic acid (cyclic-GpAp), cyclic bis(3'-5')guanylic/inosinic acid (cyclic-GpIp) and monophosphorothioic acid of cyclic-di-GMP (cyclic-GpGps) for effects on the biofilm formation of Staphylococcus aureus and Pseudomonas aeruginosa. We constructed a knockout mutant of SA0701, which is a GGDEF motif protein relevant to diguanylate cyclase from S. aureus 2507. We confirmed that the biofilm formation of this mutant (MS2507 Delta SA0701) was reduced. Cyclic-di-GMP corresponding to physiological intracellular levels given in the culture recovered the biofilm formation of MS2507 Delta SA0701, whereas its analogs did not, indicating that unlike a previous suggestion, cyclic-di-GMP was involved in the positive regulation of the biofilm formation of S. aureus and its action was structurally specific. At a high concentration (200 microM), cyclic-di-GMP and its analogs showed suppression effects on the biofilm formation of S. aureus and P. aeruginosa, and according to the quantification study using costat analysis, the suppression potential was in the order of cyclic-di-GMP, cyclic-GpGps, cyclic-GpAp and cyclic-GpIp, suggesting that the suppression effect was not strictly specific and the change of base structure quantitatively affected the suppression activity.
环状双(3'-5')二鸟苷酸(环状二鸟苷酸,cyclic-di-GMP)作为第二信使在多种细菌中发挥作用,引发广泛的生理变化。我们测量了环状二鸟苷酸及其结构类似物,如环状双(3'-5')鸟苷/腺苷酸(环状-GpAp)、环状双(3'-5')鸟苷/肌苷酸(环状-GpIp)和环状二鸟苷酸的单磷硫代酸(环状-GpGps)对金黄色葡萄球菌和铜绿假单胞菌生物膜形成的影响。我们构建了 SA0701 的敲除突变体,该蛋白是金黄色葡萄球菌 2507 中与双鸟苷酸环化酶相关的 GGDEF 基序蛋白。我们证实,该突变体(MS2507ΔSA0701)的生物膜形成减少。与培养物中生理细胞内水平相对应的环状二鸟苷酸恢复了 MS2507ΔSA0701 的生物膜形成,而其类似物则没有,这表明与之前的观点不同,环状二鸟苷酸参与了金黄色葡萄球菌生物膜形成的正调控,其作用具有结构特异性。在高浓度(200 μM)下,环状二鸟苷酸及其类似物对金黄色葡萄球菌和铜绿假单胞菌的生物膜形成表现出抑制作用,并且根据使用成本分析的定量研究,抑制潜力依次为环状二鸟苷酸、环状-GpGps、环状-GpAp 和环状-GpIp,表明抑制作用不是严格特异性的,碱基结构的变化定量影响抑制活性。