Laboratoire des Biotechnologies Végétales Appliquées à l'Amélioration des Cultures, Faculté des Sciences de Sfax, Route de Soukra km 4, B.P. 1171, 3018, Sfax, Tunisia.
Planta. 2012 Nov;236(5):1599-613. doi: 10.1007/s00425-012-1713-z. Epub 2012 Jul 29.
Proteomics analysis has been performed in leaf tissue from field date palm trees showing the brittle leaf disease (BLD) or maladie des feuilles cassantes, the main causal agent of the date palm decline in south Tunisia. To study the evolution of the disease, proteins from healthy and affected leaves taken at three disease stages (S1, S2 and S3) were trichloroacetic acid acetone extracted and subjected to two-dimensional gel electrophoresis (5-8 pH range). Statistical analysis showed that the protein abundance profile is different enough to differentiate the affected leaves from the healthy ones. Fifty-eight variable spots were successfully identified by matrix-assisted laser desorption ionization time of flight, 60 % of which corresponded to chloroplastic ones being involved in the photosynthesis electronic chain and ATP synthesis, metabolic pathways implicated in the balance of the energy, and proteases. Changes in the proteome start at early disease stage (S1), and are greatest at S2. In addition to the degradation of the ribulose-1.5-bisphosphate carboxylase oxygenase in affected leaflets, proteins belonging to the photosynthesis electronic chain and ATP synthesis decreased following the disease, reinforcing the relationship between BLD and manganese deficiency. The manganese-stabilizing proteins 33 kDa, identified in the present work, can be considered as protein biomarkers of the disease, especially at early disease step.
已对表现出脆性叶病(BLD)或“maladie des feuilles cassantes”的田间椰枣树的叶片组织进行了蛋白质组学分析,BLD 是突尼斯南部椰枣树衰退的主要致病因子。为了研究疾病的演变,从健康和受影响的叶片中提取了三个疾病阶段(S1、S2 和 S3)的三氯乙酸丙酮提取物,并进行了二维凝胶电泳(5-8 pH 范围)。统计分析表明,蛋白质丰度图谱的差异足以将受影响的叶片与健康叶片区分开来。通过基质辅助激光解吸电离飞行时间成功鉴定了 58 个可变斑点,其中 60%与参与光合作用电子链和 ATP 合成的质体有关,这些途径与能量平衡和蛋白酶有关。蛋白质组的变化始于疾病早期(S1),在 S2 时最大。除了受影响的小叶中 1.5-二磷酸核酮糖羧化酶加氧酶的降解外,光合作用电子链和 ATP 合成的蛋白质也随着疾病而减少,这加强了 BLD 与锰缺乏之间的关系。本研究中鉴定的 33 kDa 锰稳定蛋白可被视为该疾病的蛋白质生物标志物,尤其是在疾病早期阶段。