Department of Genetics and Microbiology, Faculty of Science, Charles University, Viničná 5, 128 44 Prague 2, Czech Republic.
Department of Plant Physiology and Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30 387 Krakow, Poland; Malopolska Centre of Biotechnology, Jagiellonian University, Gronostajowa 7A, 30-387 Krakow, Poland.
Biochim Biophys Acta Biomembr. 2018 Mar;1860(3):718-727. doi: 10.1016/j.bbamem.2017.12.015. Epub 2017 Dec 19.
After cold shock, the Bacillus subtilis desaturase Des introduces double bonds into the fatty acids of existing membrane phospholipids. The synthesis of Des is regulated exclusively by the two-component system DesK/DesR; DesK serves as a sensor of the state of the membrane and triggers Des synthesis after a decrease in membrane fluidity. The aim of our work is to investigate the biophysical changes in the membrane that are able to affect the DesK signalling state. Using linear alcohols (ethanol, propanol, butanol, hexanol, octanol) and benzyl alcohol, we were able to suppress Des synthesis after a temperature downshift. The changes in the biophysical properties of the membrane caused by alcohol addition were followed using membrane fluorescent probes and differential scanning calorimetry. We found that the membrane fluidization induced by alcohols was reflected in an increased hydration at the lipid-water interface. This is associated with a decrease in DesK activity. The addition of alcohol mimics a temperature increase, which can be measured isothermically by fluorescence anisotropy. The effect of alcohols on the membrane periphery is in line with the concept of the mechanism by which two hydrophilic motifs located at opposite ends of the transmembrane region of DesK, which work as a molecular caliper, sense temperature-dependent variations in membrane properties.
冷休克后,枯草芽孢杆菌去饱和酶 Des 将双键引入到现有膜磷脂的脂肪酸中。Des 的合成仅受双组分系统 DesK/DesR 调控;DesK 作为膜状态的传感器,在膜流动性降低后触发 Des 的合成。我们的工作旨在研究能够影响 DesK 信号状态的膜的生物物理变化。使用线性醇(乙醇、丙醇、丁醇、己醇、辛醇和苄醇),我们能够在温度下降后抑制 Des 的合成。通过膜荧光探针和差示扫描量热法跟踪醇添加引起的膜生物物理性质的变化。我们发现,醇诱导的膜流化反映在脂质-水界面处的水合作用增加。这与 DesK 活性的降低有关。醇的添加模拟了温度的升高,可以通过荧光各向异性等温测量来测量。醇对膜周围环境的影响符合这样一种概念,即位于 DesK 的跨膜区域两端的两个亲水基序作为分子卡尺,感知膜性质随温度的变化。