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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol outlines the visualization and quantification of a particular protein within cells at the cellular level for the phycoerythrin-containing cyanobacterium, Crocosphaera watsonii.

Abstract

Presented is a protocol for visualizing and quantifying a specific protein in cells at the cellular level for the marine cyanobacterium Crocosphaera watsonii, a crucial primary producer and nitrogen fixer in oligotrophic oceans. One of the challenges for marine autotrophic N2 fixers (diazotrophs) is distinguishing probe-derived fluorescence signals from autofluorescence. C. watsonii was selected to represent chlorophyll-, phycoerythrin- and phycourobilin-containing cyanobacteria. The protocol allows for simple and semi-quantitative visualization of proteins in C. watsonii at a single-cell level, enabling investigation of protein production under different environmental conditions to evaluate the metabolic activities of the target cyanobacteria. Furthermore, the fixation and permeabilization methods are optimized to enhance the fluorescence signals from target proteins to distinguish them from autofluorescence, especially from phycoerythrin and phycourobilin. The enhanced signal can be visualized using confocal or widefield fluorescence microscopy. Additionally, fluorescence intensity was semi-quantified using Fiji software. This single-cell analysis workflow allows the evaluation of cell-to-cell variations of specific protein content. The protocol can be performed in any life science laboratory as it requires only standard equipment and can also be easily adapted to other phycoerythrin-containing cyanobacterial cells.

Introduction

The physiological variation from cell to cell (commonly referred to as "heterogeneity") in metabolic activities within microorganisms, including cyanobacteria, has been documented through studies on clone cultures1,2,3,4. This heterogeneity encompasses diverse metabolic activities such as cell division5, carbon assimilation6,7,8, and nitrogen assimilation9,10.....

Protocol

1. Cyanobacteria cultivation

  1. Cultivate Crocosphaera watsonii PS0609 cells in Erlenmeyer flasks or photobioreactors in YBCII medium27. To determine the culture density, measure the cell density using a method of choice (e.g., microscopy, flow cytometry, cell counter, etc.).
  2. Maintain the cell densities between ~1 × 104 to ~5 × 106 cells mL-1.

2. Preparation of reagents<.......

Representative Results

The fluorescence signal was observed from extracellular substances in the negative control, where the 1st antibody was not used (Figure 1A-C). The fluorescence signal of the tyramide-boosted reagent, conjugated to the large subunit of the Rubisco protein (RbcL), was successfully detected in C. watsonii under a fluorescence microscope using a DAPI filter with UV excitation (Figure 1D-F.......

Discussion

For cyanobacteria, the TSA system has found widespread use in TSA-fluorescence in situ hybridization (TSA-FISH, CARD-FISH), targeting specific rRNA. However, its application for proteins remains limited26. In this study, a TSA procedure was applied to enable whole-cell immunodetection of the N2-fixing cyanobacterium C. watsonii, incorporating modifications based on a previous reference20. Notable revisions encompassed permeabilization, acco.......

Acknowledgements

We appreciate Dr. Radek Kana and Barbora Šedivá for assistance with confocal microscopic analysis and Dr. Roman Sobotka and Dr. Kateřina Bišová for advice in immunodetection and fluorescence microscopy analysis. This research was financially supported by Czech Research Foundation GAČR (project 20-17627S to OP and TM), the Mobility plus project between JSPS and Czech Academy of Sciences (JPJSBP 120222502), and JSPS KAKENHI (project 23H02301).

....

Materials

NameCompanyCatalog NumberComments
AchromopeptidaseFUJIFILM014-09661
Alexa Fluor350Thermo ScientificB40952Tyramide-350
Alexa Fluor405Thermo ScientificB48254Tyramide-405
Alexa Fluor488 Tyramide SuperBoost KitThermo ScientificB40922Goat anti-rabbit IgG
Bovine serum albuminSigma-AldrichA2153
CentrifugeEppendorf5804 R
Centrifuge tubes (15 mL)VWR525-1085For harvesting cells
Confocal microscopeZeissLSM880 Equipped with Airyscan
Fluorescence microscopeOlympusBX51DAPI filter: Ex.360-370 nm, Em. 420-460 nm
GelatineMerk4070
High precision microscope cover glasses for confocal microscopeDeckgläserNo. 1.5H
Liquid Blocker Regular/MiniDaido Sangyo Co., Ltd.Part 6505For keeping the cells on the slide glass
LysozymeITW ReagentsA4972
MethanolCarl Roth67-56-1
Monopotassium PhosphatePenta12290
Monunting mediumSigma-Aldrich345789-20MLFluorSave Reagent
Mounting mediumVectashildH-1300
Objective lens used in the confocal microscopeZeissPlan-Apochromat 63x/1.4 Oil DIC M27
ParaformaldehydeSigma-Aldrich158127
Poly-lysine coated slide glassSigma-AldrichP0425-72EA
Potassium chloride Lach-Ner
Safe lock tube (1.5 mL)Eppendorf0030 120.086For treating cells and storing chemicals
Sodium chloride Penta16610
Sodium hydrogen phosphate Penta15130
Triton X-100Sigma-AldrichX100

References

  1. Ackermann, M. A functional perspective on phenotypic heterogeneity in microorganisms. Nature Reviews Microbiology. 13 (8), 497-508 (2015).
  2. Schreiber, F., Ackermann, M. Environmental drivers of metaboli....

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ImmunocytochemistryProtein VisualizationCyanobacteriaCrocosphaera WatsoniiAutofluorescencePhycoerythrinPhycourobilinConfocal MicroscopyFluorescence QuantificationSingle cell Analysis

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