Li Feng-Min, Hu Hong-Ying, Chong Yun-Xiao, Guo Mei-Ting, Men Yu-Jie
State Key Joint Laboratory of Environmental Simulation and Pollution Control, Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084, China.
Huan Jing Ke Xue. 2007 Nov;28(11):2453-6.
Efflux of K+, Mg2+, Ca2+ ions from algal cells as signals of cell membrane permeability, inductively coupled plasma mass spectrometry (ICP-MS) as detection method of ions, the present research investigated effects of allelochemical eathyl-2-methyl acetoacetate (EMA) isolated from Phragmites communis on cell membrane permeability of Microcystis aeruginosa, Chlorella pyrenoidosa and Chlorella vulagaris. The results showed that, when the cells were boiled for 10 min and the membrane was destroyed absolutely, the K+ efflux of M. aeruginosa and C. pyrenoidosa were 1.45 and 1.59 microg x (10(9) cell) (-1), respectively. When the concentration of EMA was 2 mg x L(-1), the K+ efflux of M. aeruginosa and C. pyrenoidosa were 1.38 and 1.40 microg x (10(9) cell)(-1), respectively. The K+ efflux of M. aeruginosa and C. pyrenoidosa reached 1.44 and 1.58 microg x (10(9) cell)(-1) while the EMA was 4 mg x L(-1). When the concentrations were 2 mg x L(-1) or 4 mg x L(-1) the K+ efflux reached more than 95% of the total ion amount in M. aeruginosa and C. pyrenoidosa cells. But when EMA concentration was 4 mg x L(-1), K+ efflux of C. vulagaris was 0.64 microg x (10(9) cell)(-1), which was only 31.5% of total K+ amount in C. vulagaris. Effects EMA on efflux of Mg2+ and Ca2+ were similar to those of K+. The results indicated that EMA destroyed the cell membrane of M. aeruginosa and C. pyrenoidosa but not C. vulagaris. This is one of the mechanisms of EMA species-selective antialgal.
钾离子、镁离子、钙离子从藻类细胞外流作为细胞膜通透性的信号,电感耦合等离子体质谱法(ICP-MS)作为离子检测方法,本研究调查了从芦苇中分离出的化感物质乙基-2-甲基乙酰乙酸酯(EMA)对铜绿微囊藻、蛋白核小球藻和普通小球藻细胞膜通透性的影响。结果表明,当细胞煮沸10分钟且细胞膜被完全破坏时,铜绿微囊藻和蛋白核小球藻的钾离子外流分别为1.45和1.59微克×(10⁹个细胞)⁻¹。当EMA浓度为2毫克×升⁻¹时,铜绿微囊藻和蛋白核小球藻的钾离子外流分别为1.38和1.40微克×(10⁹个细胞)⁻¹。当EMA为4毫克×升⁻¹时,铜绿微囊藻和蛋白核小球藻的钾离子外流分别达到1.44和1.58微克×(10⁹个细胞)⁻¹。当浓度为2毫克×升⁻¹或4毫克×升⁻¹时,铜绿微囊藻和蛋白核小球藻细胞中的钾离子外流达到总离子量的95%以上。但当EMA浓度为4毫克×升⁻¹时,普通小球藻的钾离子外流为0.64微克×(10⁹个细胞)⁻¹,仅为普通小球藻总钾离子量的31.5%。EMA对镁离子和钙离子外流的影响与对钾离子的影响相似。结果表明,EMA破坏了铜绿微囊藻和蛋白核小球藻的细胞膜,但未破坏普通小球藻的细胞膜。这是EMA具有物种选择性抑藻作用的机制之一。