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Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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 developed.
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

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...
Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

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...

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An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images
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An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images

Published on: August 31, 2012

Multidimensional single-cell analysis based on fluorescence microscopy and automated image analysis.

Michael Sandmann1, Martin Lippold2, Franziska Saalfrank2

  • 1Institute for Food and Environmental Research (ILU e. V.), Arthur-Scheunert-Allee 40-41, 14558, Nuthetal, Germany. michael.sandmann@ilu-ev.de.

Analytical and Bioanalytical Chemistry
|April 19, 2017
PubMed
Summary

A new single-cell analysis method using epifluorescence microscopy reveals significant cell-to-cell variations in chlorophyll content and density in green algae cultures. This heterogeneity impacts understanding algal physiology and biomass production.

Keywords:
ChlorophyllMultidimensional single-cell analysisObject recognitionWide-field fluorescence microscopy

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Analysis of Multidimensional Microscopy Data Using Cell-ACDC

Published on: November 7, 2025

Area of Science:

  • Biotechnology
  • Cell Biology
  • Microscopy

Background:

  • Fast-growing microalgae are crucial for biomass production.
  • Understanding cellular heterogeneity is vital for optimizing algal cultivation and metabolic studies.

Purpose of the Study:

  • To develop and validate a single-cell analytical technology for evaluating fast-growing green algae.
  • To investigate cell-to-cell heterogeneity in key physiological parameters.

Main Methods:

  • Epifluorescence microscopy-based cytometry.
  • Automated image analysis with single-threshold discrimination.
  • Reference analyses for validation of object recognition, particle size, and chlorophyll determination.

Main Results:

  • The developed technique reliably assesses single-cell parameters.
  • Algal cells (Acutodesmus o.) exhibited significant heterogeneity in size, chlorophyll amount, and density.
  • High correlation between cell size and chlorophyll amount, but low correlation with chlorophyll density was observed.

Conclusions:

  • Single-cell analysis reveals substantial variations in the photosynthetic apparatus architecture and physiological state within algal populations.
  • This heterogeneity must be considered in systems biology models of algal biomass accumulation and metabolism.