Department of Stress Biology and Plant Pathology, Centro de Edafología y Biología Aplicada del Segura (CEBAS-CSIC), P.O. Box 164, E-30100 Murcia, Spain.
J Plant Physiol. 2011 Apr 15;168(6):566-75. doi: 10.1016/j.jplph.2010.09.012. Epub 2010 Nov 12.
The effects of an oligogalacturonic acid (OGA) pool on root length of intact alfalfa seedlings (Medicago sativa L.), on extracellular pH and on both extracellular and intracellular O₂⁻ dynamics were examined in this study. Lower OGA concentrations (25, 50 and 75 μg mL⁻¹)promoted root length, but 50 μg mL⁻¹ had a stronger effect in promoting growth, while the higher OGA concentration (100 μg mL⁻¹)had no significant effect. Extracellular alkalinization was tested only at concentrations higher than 50 μg mL⁻¹ OGA, showing that the response is determined not only by the specific size of OGA, but also by the concentration of OGA. The promoting effect of OGA on root growth at 25, 50 and 75 μg mL⁻¹ OGA concentrations in alfalfa root appeared to be unrelated to extracellular alkalinization. A possible explanation could be the induction of an O₂⁻ burst at non-toxic levels, which could drive directly or indirectly several processes associated with root elongation in 25, 50 and 75 μg mL⁻¹ OGA-treated seedlings. Analyses using confocal microscopy showed that the increase in the O₂⁻ generation, mainly in the epidermal cells, induced by 50 μg mL⁻¹ OGA could be related to the promoting effect on root growth. The combination of OGA with DPI allowed us to demonstrate that there are different O₂⁻-generating sources in the epidermal cells of the meristematic zone, likely NADPH oxidase and oxidases or oxido-reductase enzymes, insensitive to DPI, that maintain detectable O₂⁻ accumulation at 60 and 120 min of treatment. These results suggest that OGA induce an oxidative burst by several O₂⁻-generating sources in the active growth zones.
本研究考察了低聚半乳糖醛酸(OGA)库对完整紫花苜蓿幼苗(Medicago sativa L.)根长、细胞外 pH 值以及细胞外和细胞内 O₂⁻动态的影响。较低浓度的 OGA(25、50 和 75μg mL⁻¹)促进根长,但 50μg mL⁻¹对生长的促进作用更强,而较高浓度的 OGA(100μg mL⁻¹)则没有显著影响。仅在 OGA 浓度高于 50μg mL⁻¹时才检测到细胞外碱化,表明这种反应不仅取决于 OGA 的特定大小,还取决于 OGA 的浓度。在紫花苜蓿根中,25、50 和 75μg mL⁻¹ OGA 浓度下 OGA 对根生长的促进作用似乎与细胞外碱化无关。一种可能的解释是,在非毒性水平下诱导 O₂⁻爆发,这可能直接或间接地驱动与 25、50 和 75μg mL⁻¹ OGA 处理的幼苗中根伸长相关的几个过程。共聚焦显微镜分析表明,50μg mL⁻¹ OGA 诱导的 O₂⁻生成增加主要发生在表皮细胞中,这可能与促进根生长有关。OGA 与 DPI 的组合使我们能够证明在分生区的表皮细胞中有不同的 O₂⁻产生来源,可能是 NADPH 氧化酶和氧化酶或氧化还原酶,对 DPI 不敏感,在处理 60 和 120 分钟时仍能维持可检测的 O₂⁻积累。这些结果表明,OGA 通过分生区的几个 O₂⁻产生源诱导氧化爆发。