Fagioni Marco, D'Amici Glan Maria, Timperio Anna Maria, Zolla Lello
Department of Environmental Sciences, Tuscia University, Viterbo, Italy.
J Proteome Res. 2009 Jan;8(1):310-26. doi: 10.1021/pr800507x.
The time course of the thylakoid membranes proteomic profile changes upon cadmium (Cd) addition to hydroponic Spinacia oleracea L. plants has been investigated. Two different proteomic approaches have been used: blue native gel electrophoresis followed by SDS-PAGE (2D BN-SDS-PAGE) and sucrose density gradient ultracentrifugation followed by RP-HPLC. Chlorophyll (Chl) and xanthophylls concentrations, together with ESR and real time PCR measurements, were also performed to get a complete overview of all photosystem changes. Cd only accumulated in basal leaves, that therefore were prevalently investigated for assessment of Cd induced changes. Here, Cd strongly reduced Chl concentration, especially Chl a. During the first 15 days of treatment, native electrophoresis system revealed high sensitivity of PSI to Cd, while minor effects on PSII were observed. Cytochrome b(6)/f and the ATP-synthase complex did not change following the Cd treatment. A significant reduction of antenna proteins of PSI was observed, while PSII antennae were affected to a minor extent, with exception of the isomeric Lhcb1.1 which decreased significantly already at the onset of the treatment. Some PSII core proteins were overexpressed, but showed reduced activity. No new protein was formed and no specific protein disappeared in the photosynthetic apparatus of Cd-treated leaves. Upon removal of Cd, a rapid resynthesis of total Chl and a significant resynthesis of Lhcb1.1 antenna were observed, suggesting that Cd affects specifically the photosynthetic apparatus of spinach basal leaves, replacing other metal ions inside proteins.
研究了水培菠菜(Spinacia oleracea L.)植株添加镉(Cd)后类囊体膜蛋白质组学图谱变化的时间进程。采用了两种不同的蛋白质组学方法:蓝色非变性凝胶电泳后进行SDS-PAGE(二维蓝色非变性- SDS-PAGE)和蔗糖密度梯度超速离心后进行反相高效液相色谱(RP-HPLC)。还进行了叶绿素(Chl)和叶黄素浓度测定,以及电子自旋共振(ESR)和实时定量PCR测量,以全面了解所有光合系统的变化。Cd仅在基部叶片中积累,因此主要对基部叶片进行研究以评估Cd诱导的变化。在此,Cd强烈降低了Chl浓度,尤其是Chl a。在处理的前15天,非变性电泳系统显示PSI对Cd高度敏感,而对PSII的影响较小。细胞色素b6/f和ATP合酶复合体在Cd处理后没有变化。观察到PSI的天线蛋白显著减少,而PSII天线受到的影响较小,但异构的Lhcb1.1除外,其在处理开始时就已显著下降。一些PSII核心蛋白过度表达,但活性降低。在Cd处理的叶片光合装置中没有形成新蛋白,也没有特定蛋白消失。去除Cd后,观察到总Chl快速重新合成以及Lhcb1.1天线显著重新合成,这表明Cd特异性地影响菠菜基部叶片的光合装置,取代了蛋白质中的其他金属离子。