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Related Concept Videos

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Recombinant DNA technology called transgenesis is often used to add a foreign gene or remove a detrimental gene from an organism. Such genetically modified organisms are called transgenic organisms.
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A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred...
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Plant tissue culture is widely used in both primary and applied science. Applications range from plant development studies to functional gene studies, crop improvement, commercial micropropagation, virus elimination, and conservation of rare species.
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Related Experiment Video

Updated: Oct 1, 2025

Efficient Polyethylene Glycol PEG Mediated Transformation of the Moss Physcomitrella patens
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Physcomitrium patens Protoplasting and Protoplast Transfection.

Florence Charlot1, Guillaume Goudounet1, Fabien Nogué1

  • 1Institut Jean-Pierre Bourgin, INRAE, AgroParisTech, Université Paris-Saclay, Versailles, France.

Methods in Molecular Biology (Clifton, N.J.)
|March 8, 2022
PubMed
Summary

This study standardizes protoplast production in Physcomitirella patens, enhancing genetic studies and bioengineering. A new alginate embedding method improves protoplast survival and regeneration efficiency.

Keywords:
AlginateCRISPR-Cas9Homologous recombinationPEG-mediated transfectionPhyscomitrella patensProtoplastReverse genetics

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Area of Science:

  • Plant biology
  • Moss biotechnology
  • Molecular genetics

Background:

  • Physcomitrella patens protoplasts are crucial for reverse genetics and protein production.
  • Existing protocols require optimization for consistency and efficiency.

Purpose of the Study:

  • To present a standardized protocol for Physcomitirella patens protoplast production.
  • To detail transfection, regeneration, and selection methods.
  • To introduce an improved protoplast embedding technique.

Main Methods:

  • Standardized protoplast isolation from P. patens protonemata.
  • Procedures for protoplast transfection, plating, and selection.
  • Development of an alginate matrix for protoplast embedding and regeneration.

Main Results:

  • A consistent and standardized protocol for protoplast production and manipulation.
  • Successful transfection and regeneration of P. patens protoplasts.
  • Alleviation of warm agarized medium, optimizing transformed protoplast survival.

Conclusions:

  • The standardized protocol and alginate embedding enhance protoplast regeneration efficiency.
  • This method supports advanced genetic studies and bioengineering applications in P. patens.
  • The protocol offers a robust tool for moss biotechnology research.