Pomology Department, Estación Experimental de Aula Dei, CSIC, Apartado 13034, E-50080 Zaragoza, Spain.
J Plant Physiol. 2011 Jun 15;168(9):887-93. doi: 10.1016/j.jplph.2010.11.017. Epub 2011 Feb 8.
Two Prunus rootstocks, the Myrobalan plum P 2175 and the interspecific peach-almond hybrid, Felinem, were studied to characterize their biochemical and molecular responses induced under iron-Deficient conditions. Plants of both genotypes were submitted to different treatments using a hydroponic system that permitted removal of Fe from the nutrient solution. Control plants were grown in 90 μM Fe (III)-EDTA, Deficient plants were grown in an iron free solution, and plants submitted to an Inductor treatment were resupplied with 180 μM Fe (III)-EDTA over 1 and 2 days after a period of 4 or 15 days of growth on an iron-free solution. Felinem increased the activity of the iron chelate reductase (FC-R) in the Inductor treatment after 4 days of iron deprivation. In contrast, P 2175 did not show any response after at least 15 days without iron. The induction of the FC-R activity in this genotype was coincident in time with the medium acidification. These results suggest two different mechanisms of iron chlorosis tolerance in both Strategy I genotypes. Felinem would use the iron reduction as the main mechanism to capture the iron from the soil, and in P 2175, the mechanism of response would be slower and start with the acidification of the medium synchronized with the gradual loss of chlorophyll in leaves. To better understand the control of these responses at the molecular level, the differential expression of PFRO2, PIRT1 and PAHA2 genes involved in the reductase activity, the iron transport in roots, and the proton release, respectively, were analyzed. The expression of these genes, estimated by quantitative real-time PCR, was different between genotypes and among treatments. The results were in agreement with the physiological responses observed.
两种桃砧木,李属扁桃 P 2175 和李属桃-扁桃杂种费利内姆,研究了它们在缺铁条件下诱导的生化和分子反应特征。使用允许从营养液中去除铁的水培系统,将两种基因型的植物分别进行不同处理。对照植物在 90 μM Fe(III)-EDTA 中生长,缺铁植物在无铁溶液中生长,而在诱导处理中,植物在缺铁溶液中生长 4 或 15 天后,用 180 μM Fe(III)-EDTA 再供应 1 或 2 天。在缺铁 4 天后,费利内姆增加了诱导剂处理中铁螯合还原酶(FC-R)的活性。相比之下,P 2175 在至少 15 天没有铁的情况下没有任何反应。该基因型中 FC-R 活性的诱导与培养基酸化时间一致。这些结果表明两种策略 I 基因型对缺铁性黄化的耐受性有两种不同的机制。费利内姆将使用铁还原作为从土壤中获取铁的主要机制,而在 P 2175 中,响应机制将较慢,从与叶片中叶绿素逐渐丧失同步的培养基酸化开始。为了更好地理解这些分子水平上的控制,分析了参与还原酶活性、根系铁运输和质子释放的 PFRO2、PIRT1 和 PAHA2 基因的差异表达。通过定量实时 PCR 估计这些基因的表达在基因型和处理之间不同。结果与观察到的生理反应一致。