首页> 外文期刊>Journal of Microscopy >Microwave-assisted rapid plant sample preparation for transmission electron microscopy.
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Microwave-assisted rapid plant sample preparation for transmission electron microscopy.

机译:微波辅助快速植物样品的制备,用于透射电子显微镜。

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The preparation of plant leaf material for transmission electron microscopical investigations can be a very time- and labour-consuming task as the reagents infiltrate the samples quite slowly and as usually most steps have to be performed manually. Fixation, buffer washes, dehydration, resin infiltration and polymerization of the resin-infiltrated leaf samples can take several days before the specimen can be cut ultrathin and used for ultrastructural investigations. In this study, we present a microwave-assisted automated sample preparation procedure that reduces preparation time from at least 3 days to about 5 h - with only a few steps that have to be performed manually - until the plant sample can be ultrathin sectioned and observed with the transmission electron microscope. For studying the efficiency of this method we have compared the ultrastructure of different leaf material (Arabidopsis thaliana, Nicotiana tabacum and Picea abies) which was prepared with a conventional, well-established chemical fixation and embedding protocol and a commercially available automated microwave tissue processor. Despite the massive reduction in sample preparation time no negative effects on cutting properties of the blocks, stability of the sections in the electron beam, contrast and ultrastructure of the cells were observed under the transmission electron microscope when samples were prepared with the microwave-assisted protocol. Additionally, no negative effects were detected on the dimensions of fine structures of grana stacks (including membranes, inter- and intrathylakoidal spaces), the nuclear envelope and the plasma membrane as the diameter of these structural components did not differ between leaf samples (of the same species) that were processed with the automated microwave tissue processor or by conventional fixation and embedding at room temperature.
机译:制备用于透射电子显微镜研究的植物叶片材料可能是非常耗时和费力的任务,因为试剂相当缓慢地渗透样品,并且通常大多数步骤必须手动进行。树脂浸润的叶片样品的固定,缓冲液洗涤,脱水,树脂浸润和聚合过程可能需要几天,然后才能将样品超薄切割并用于超微结构研究。在这项研究中,我们提出了一种微波辅助的自动样品制备程序,该程序将制备时间从至少3天减少到大约5小时-仅需手动执行几个步骤-直到可以对植物样品进行超薄切片和观察为止用透射电子显微镜。为了研究这种方法的效率,我们比较了不同叶片材料(拟南芥,烟草和云杉)的超微结构,这些叶片是用常规的,行之有效的化学固定和包埋方案以及可商购的自动微波组织处理器制备的。尽管大大减少了样品制备时间,但在采用微波辅助方案制备样品的情况下,在透射电镜下仍未观察到块的切割性能,电子束截面的稳定性,细胞的对比度和超微结构的负面影响。 。此外,未检测到对谷物堆叠的精细结构(包括膜,类囊体内部和类囊体内部空间),核被膜和质膜的尺寸产生负面影响,因为这些结构成分的直径在叶片样品之间(相同的物种),使用自动微波组织处理器或常规固定方法并在室温下嵌入进行处理。

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