Mayer Moritz, Schug Christina, Geimer Stefan, Klecker Till, Westermann Benedikt
Zellbiologie und Elektronenmikroskopie, Universität Bayreuth Bayreuth, 95440 Germany.
Microb Cell. 2024 Nov 18;11:378-386. doi: 10.15698/mic2024.11.840. eCollection 2024.
Budding yeast is widely used as a model organism to study the biogenesis and architecture of organellar membranes, which can be visualized by transmission electron microscopy (TEM). Preparation of yeast cells for TEM can be quite challenging and time-consuming. Here, we describe an optimized protocol for conventional fixation of yeast cells with potassium permanganate combined with cell wall permeabilization with sodium metaperiodate and embedding in Epon. We have replaced time-consuming incubation steps by short treatments with microwaves and developed a microwave-assisted permanganate fixation and Epon embedding protocol that reduces the time required for sample preparation to one working day. We expect that these protocols will be useful for routine analysis of membrane ultrastructure in yeast.
芽殖酵母被广泛用作研究细胞器膜生物发生和结构的模式生物,通过透射电子显微镜(TEM)可以观察到这些细胞器膜。为TEM制备酵母细胞颇具挑战性且耗时。在此,我们描述了一种优化方案,即先用高锰酸钾对酵母细胞进行常规固定,再用过碘酸钠使细胞壁通透,并嵌入环氧树脂。我们用微波短时间处理取代了耗时的孵育步骤,开发出一种微波辅助高锰酸钾固定和环氧树脂嵌入方案,将样品制备所需时间缩短至一个工作日。我们期望这些方案对酵母膜超微结构的常规分析有用。