Ali Mohammad Babar, Hahn Eun-Joo, Paek Kee-Yoeup
National Food Research Institute, Cell Function Laboratory, Tsukuba, Ibaraki-305-8642, Japan.
Plant Cell Rep. 2006 Oct;25(10):1122-32. doi: 10.1007/s00299-006-0174-x. Epub 2006 Jun 29.
Roots of Panax ginseng exposed to various concentrations of Cu (0.0, 5, 10.0, 25.0, and 50.0 microM) accumulated high amounts of Cu in a concentration-dependent and duration-dependent manner. Roots treated with 50 microM Cu resulted in 52% and 89% growth inhibition after 20 and 40 days, respectively. Saponin synthesis was stimulated at a Cu concentration between 5 and 25 muM but decreased at 50 microM Cu. Malondialdehyde content (MDA), lipoxygenase activity (LOX), superoxide ion (O2*-) accumulation, and H2O2 content at 5 and 10 microM Cu-treated roots were not increased but strongly increased at 50 microM Cu resulting in the oxidation of ascorbate (ASC) and glutathione (GSH) to dehydroascorbate (DHA) and glutathione disulfide (GSSG), respectively indicating a clear oxidative stress. Seven well-resolved bands of superoxide dismutase (SOD) were detected in the gel and an increase in SOD activity seemed to be mainly due to the induction of Fe-SOD 3. Five to 10 microM Cu slightly induced activity of ascorbate peroxidase (APX) and dehydroascorbate reductase (DHAR), guaiacol peroxidase (G-POD) but inhibited monodehydroascorbate reductase (MDHAR) and glutathione reductase (GR) enzyme activities. No changes in catalase (CAT) activity and in activity gel were found up to 25 microM Cu, but both G-POD and CAT activities were inhibited at 50 microM Cu. Glutathione metabolism enzymes such as gamma-glutamylcysteine synthetase (gamma-GCS), glutathione-S-transferase (GST), and glutathione peroxidase activities (GPx) were activated at 5 and 10 microM Cu but were strongly inhibited at 50 microM Cu due to the Cu accumulation in root tissues. The strong depletion of GSH at 50 microM Cu was associated to the strong induction of gamma-glutamyltranspeptidase (gamma-GGT) activity. These results indicate that plant could grow under Cu stress (5-25 microM) by modulating the antioxidant defense mechanism for combating Cu induced oxidative stress.
人参根暴露于不同浓度的铜(0.0、5、10.0、25.0和50.0微摩尔)时,会以浓度依赖性和时间依赖性方式积累大量铜。用50微摩尔铜处理的根在20天和40天后分别导致52%和89%的生长抑制。在5至25微摩尔的铜浓度下,皂苷合成受到刺激,但在50微摩尔铜时减少。在5和10微摩尔铜处理的根中,丙二醛含量(MDA)、脂氧合酶活性(LOX)、超氧离子(O2*-)积累和过氧化氢含量没有增加,但在50微摩尔铜时强烈增加,导致抗坏血酸(ASC)和谷胱甘肽(GSH)分别氧化为脱氢抗坏血酸(DHA)和谷胱甘肽二硫化物(GSSG),这表明存在明显的氧化应激。在凝胶中检测到七条分辨率良好的超氧化物歧化酶(SOD)条带,SOD活性的增加似乎主要是由于铁-SOD 3的诱导。5至10微摩尔铜轻微诱导抗坏血酸过氧化物酶(APX)和脱氢抗坏血酸还原酶(DHAR)、愈创木酚过氧化物酶(G-POD)的活性,但抑制单脱氢抗坏血酸还原酶(MDHAR)和谷胱甘肽还原酶(GR)的酶活性。在高达25微摩尔铜时,过氧化氢酶(CAT)活性和活性凝胶未发现变化,但在50微摩尔铜时,G-POD和CAT活性均受到抑制。谷胱甘肽代谢酶如γ-谷氨酰半胱氨酸合成酶(γ-GCS)、谷胱甘肽-S-转移酶(GST)和谷胱甘肽过氧化物酶活性(GPx)在5和10微摩尔铜时被激活,但在50微摩尔铜时由于根组织中铜的积累而受到强烈抑制。在50微摩尔铜时谷胱甘肽的强烈消耗与γ-谷氨酰转肽酶(γ-GGT)活性的强烈诱导有关。这些结果表明,植物可以通过调节抗氧化防御机制来对抗铜诱导的氧化应激,从而在铜胁迫(5至25微摩尔)下生长。