环境海洋微生物的目标体积相关光和电子显微镜
Karel Mocaer1,2, Giulia Mizzon3,4,5, Manuel Gunkel6
1Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Journal of cell science
|July 17, 2023
概括
研究人员开发了一种新的3D电子显微镜方法来研究微藻. 这种技术允许在复杂的自然环境中对单细胞进行详细的超结构分析,如恐龙鞭毛虫Ensiculifera tyrrhenica.
科学领域:
- 微生物学 微生物学
- 细胞生物学 细胞生物学
- 海洋生物学 海洋生物学
背景情况:
- 光合作用微藻对于全球碳和氧循环至关重要.
- 了解微藻细胞生物学需要先进的3D成像技术.
- 环境样本对高通量超结构分析具有挑战.
研究的目的:
- 开发和验证一个工作流程,以对自然社区中的微藻进行有针对性的3D超结构性表征.
- 为了深入了解光合作用恐龙鞭毛虫Ensiculifera tyrrhenica的细胞生物学.
主要方法:
- 使用了一种与光和体积电子显微镜 (vEM) 兼容的新型电子显微镜样品制备方法.
- 采用了一种工作流程,可以在复杂的环境样本中对单个细胞进行有针对性的成像.
- 进行了有机体和亚细胞结构的定量表征.
主要成果:
- 成功揭示了Ensiculifera tyrrhenica.的3D亚细胞景观.
- 量化多个有机体,包括单个卷曲的叶绿体.
- 描述了鞭毛器官的布置和相关的光敏感元件.
- 观察到部分染色体展开,表明永久凝聚的染色体中潜在的转录活性.
结论:
- 开发的方法提供了环境微生物的高效,有针对性的超结构分析.
- 提供了对恐龙状细胞生物学的新见解,特别是Ensiculifera tyrrhenica.
- 展示了在3D中分析异质微生物混合物的原理证明.
相关概念视频
Overview of Electron Microscopy
9.3K
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
9.3K
Two-Dimensional Microscopy in Microbiology
82
Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
82
Super-resolution Fluorescence Microscopy
7.1K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.1K
Overview of Microscopy Techniques
10.5K
The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
10.5K
Microbial Morphologies
53
Bacterial and archaeal cells exhibit remarkable diversity in shape and structure, critical in their adaptability and functionality. Among bacteria, the most commonly observed shapes include cocci and bacilli. Cocci are spherical and may exist singly or in groupings such as pairs (diplococci), chains (streptococci), clusters (staphylococci), or tetrads. Bacilli, in contrast, are rod-shaped and can also occur as single cells, in pairs, or chains, depending on their environmental and genetic...
53
Three-Dimensional Microscopy in Microbiology
68
Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
68


