首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >IMPROVED ULTRASTRUCTURAL PRESERVATION OF PETUNIA AND BRASSICA OVULES AND EMBRYO SACS BY HIGH PRESSURE FREEZING AND FREEZE SUBSTITUTION
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IMPROVED ULTRASTRUCTURAL PRESERVATION OF PETUNIA AND BRASSICA OVULES AND EMBRYO SACS BY HIGH PRESSURE FREEZING AND FREEZE SUBSTITUTION

机译:高压冷冻和冷冻替代提高了对PET,芸苔卵和胚囊的超微结构的保存

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In order to improve the ultrastructural preservation of the female gametophyte of Petunia x hybrida and Brassica napus we tested several cryofixation techniques and compared the results with those of conventional chemical fixation methods. Ovules fixed with glutaraldehyde and osmium tetroxide in the presence or absence of potassium fenocyanide showed poor cell morphological and ultrastructural preservation. In ovules cryo-fixed by plunging into liquid propane, the cell morphology was well preserved. However, at the ultrastructural level structure-distorting ice crystals were detected in all tissues. Due to the large size of the ovules, cryofixation by plunging in liquid propane is not adequate for ultrastructural studies. In contrast, P. I hybrida and B. napus ovules cryo-fixed by high pressure freezing showed improved cell morphological as well as ultrastructural preservation of the embryo sac and the surrounding integumentary tissues. The contrast of the cellular membranes after freeze substitution with 2% osmium tetroxide and 0.1% uranyl acetate in dry acetone was high. At the ultrastructural level, the most prominent improvements were: straight plasma membranes which were appressed to the cell walls; turgid appearing organelles with smooth surface contours; minimal extraction of cytoplasmic and extracellular substances. In contrast to the chemically fixed ovules, in high pressure frozen ovules numerous microtubules and multivesicular bodies could be distinguished. [References: 36]
机译:为了改善矮牵牛和甘蓝型油菜雌配子体的超微结构保存,我们测试了几种冷冻固定技术,并将结果与​​常规化学固定方法进行了比较。在存在或不存在氰氰化钾的情况下,用戊二醛和四氧化os固定的胚珠表现出较差的细胞形态和超微结构保存。在通过浸入液态丙烷而冷冻固定的胚珠中,细胞形态得到了很好的保存。然而,在超微结构水平上,在所有组织中都检测到了扭曲结构的冰晶。由于胚珠大,通过浸入液体丙烷进行冷冻固定不足以进行超微结构研究。相反,通过高压冷冻冷冻固定的P. I hybrida和B. napus胚珠显示出改善的细胞形态以及胚囊和周围的珠被组织的超微结构保存。用无水丙酮中的2%四氧化os和0.1%乙酸铀酰冷冻替代后,细胞膜的对比度很高。在超微结构方面,最显着的改进是:贴在细胞壁上的直质膜;外观光滑的光滑细胞器;最少提取细胞质和细胞外物质。与化学固定的胚珠相反,在高压冷冻的胚珠中,可以区分出许多微管和多囊泡体。 [参考:36]

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