通过电子显微镜观察微藻脂质体。

IF 1.5 4区 工程技术 Q3 MICROSCOPY
Ellen Verwee, Davy Van de Walle, Michiel De Bruyne, Esther Mienis, Mirna Sekulic, Peter Chaerle, Wim Vyverman, Imogen Foubert, Koen Dewettinck
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引用次数: 0

摘要

本研究评估了透射电子显微镜(TEM)和低温扫描电子显微镜(Cryo-SEM)检测微藻脂质体的能力。为此,研究人员采集了处于旺盛生长中期和静止生长早期的 Phaeodactylum tricornutum 和 Nannochloropsis oculata 细胞。比较了两种不同的低温扫描电镜切割方法:低温平整和冷冻切割。结果表明,尽管制备时间较长,但在冷冻固定之前进行 TEM 观察可清晰地检测脂质体,比冷冻-SEM 更为可取。使用冷冻断裂法很少能检测到脂质体。只有当内部结构中的结晶层(很可能与固醇酯或二饱和三酰甘油有关)被揭示出来时,才能检测到脂质体。此外,冷冻平铺法也无法检测到脂质体。低温扫描电镜也不是识别脂质体以外的其他细胞器的首选技术,但它确实发现了两个物种中的叶绿体,以及低温刨平的 Nannochloropsis oculata 样品中的含丝细胞器。本文受版权保护。版权所有 脂质体是一种细胞器,在细胞内起到储存脂质的作用。微藻类积累的脂质可占其干重的 50%以上。这些脂质可用于生产生物燃料和食品。某些微藻类生长速度快、产量高,是一种有趣的替代脂质来源。当细胞在营养限制等不利条件下生长时,微藻中的脂质含量会增加。本研究的目的是比较先进的显微镜技术,以观察两种不同微藻中的脂质体。第一种技术是透射电子显微镜(TEM),即在观察前对样品进行高压冷冻、冷冻替代并切成薄片。第二种技术是低温扫描电子显微镜(cryo-SEM),首先采用两种不同的切割方法来显示样品的内部结构。样品被快速冷冻后,要么被粗暴地折断(冷冻折断),要么被锋利的刀切割,以获得一个平整的表面(冷冻平整)。对每种微藻的生长中期和早期静止期细胞进行了检测,预计后者的脂质体数量更多。结果表明,先用 TEM 观察,然后再冷冻固定,可以检测到脂质体,尽管制备时间较长,但比冷冻-SEM 更优。使用冷冻断裂法只能偶尔检测到几个脂质体,因为断裂面需要穿过脂质体,显示内部结构(层),这对于脂质体的识别是必要的。冷冻平铺技术对检测这些样本中的脂质体没有帮助,因为这种技术会导致细胞表面变平。此外,TEM 能显示最多的其他细胞器,而冷冻扫描电镜只能显示叶绿体和含丝细胞器。我们的发现有助于其他研究人员选择合适的电子显微镜技术来观察生物样本中的脂质体或食品基质的微观结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visualisation of microalgal lipid bodies through electron microscopy

In this study, transmission electron microscopy (TEM) and cryo-scanning electron microscopy (cryo-SEM) were evaluated for their ability to detect lipid bodies in microalgae. To do so, Phaeodactylum tricornutum and Nannochloropsis oculata cells were harvested in both the mid-exponential and early stationary growth phase. Two different cryo-SEM cutting methods were compared: cryo-planing and freeze-fracturing. The results showed that, despite the longer preparation time, TEM visualisation preceded by cryo-immobilisation allows a clear detection of lipid bodies and is preferable to cryo-SEM. Using freeze-fracturing, lipid bodies were rarely detected. This was only feasible if crystalline layers in the internal structure, most likely related to sterol esters or di-saturated triacylglycerols, were revealed. Furthermore, lipid bodies could not be detected using cryo-planing. Cryo-SEM is also not the preferred technique to recognise other organelles besides lipid bodies, yet it did reveal chloroplasts in both species and filament-containing organelles in cryo-planed Nannochloropsis oculata samples.

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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
期刊介绍: The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit. The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens. Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.
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