Meyer Y, Grosset J, Chartier Y, Cleyet-Marel J C
Université de Perpignan Laboratoire de Physiologie Végétale, France.
Electrophoresis. 1988 Nov;9(11):704-12. doi: 10.1002/elps.1150091105.
Using phenol extraction from tobacco callus, we have prepared extracts with a high protein content. These proteins were separated in cylindrical non-equilibrium pH gradient gels and visualized by dipping in sodium dodecyl sulfate (SDS)-containing solution. Three gel sections, each containing proteins previously detected as abundantly synthesized in tobacco mesophyll protoplasts and whose synthesis is reduced by auxin application, were excised from each gel and collected. These proteins were further separated on slab SDS gels and protein bands were excised after Coomassie Brilliant Blue R-250 staining and used to inject three rabbits. After one booster, highly specific antibodies were detected in their sera by ELISA and immunoblotting. Using these sera we have confirmed that the corresponding proteins are identical in callus and mesophyll protoplast and demonstrated that they are abundantly accumulated in tobacco roots but are undetectable in aerial organs and seeds.
通过从烟草愈伤组织中进行苯酚提取,我们制备了蛋白质含量高的提取物。这些蛋白质在圆柱形非平衡pH梯度凝胶中进行分离,并通过浸入含十二烷基硫酸钠(SDS)的溶液中进行可视化。从每个凝胶中切下三个凝胶切片,每个切片都含有先前检测到在烟草叶肉原生质体中大量合成且其合成因生长素处理而减少的蛋白质。这些蛋白质在平板SDS凝胶上进一步分离,考马斯亮蓝R-250染色后切下蛋白质条带,用于注射三只兔子。一次加强免疫后,通过ELISA和免疫印迹在它们的血清中检测到高特异性抗体。使用这些血清,我们证实了愈伤组织和叶肉原生质体中的相应蛋白质是相同的,并证明它们在烟草根中大量积累,但在地上器官和种子中无法检测到。