Protoplast, from the ancient Greek πρῶτον (first) + verb πλάθω or πλάττω (to mould: deriv. plastic), initially referred to the first organized body of a species.
Protoplast has several biological definitions:
- A protoplast is a plant, bacterial or fungal cell that had its cell wall completely or partially removed using either mechanical or enzymatic means.
- Protoplasts: Have their cell wall entirely removed
- Spheroplasts: Have their cell wall only partially removed
- More generally protoplast refers to that unit of biology which is composed of a cell's nucleus and the surrounding protoplasmic materials.
Enzymes for the preparation of protoplasts
|Type of cell||Enzyme|
|Plant cells||Cellulase, pectinase, xylanase|
|Gram-positive bacteria||Lysozyme (+EDTA)|
During and subsequent to digestion of the cell wall, the protoplast becomes very sensitive to osmotic stress. This means cell wall digestion and protoplast storage must be done in an isotonic solution to prevent rupture of the plasma membrane.
Uses for protoplasts
Protoplasts are widely used for DNA transformation (for making genetically modified organisms), since the cell wall would otherwise block the passage of DNA into the cell. In the case of plant cells, protoplasts may be regenerated into whole plants first by growing into a group of plant cells that develops into a callus and then by regeneration of shoots (caulogenesis) from the callus using plant tissue culture methods. Growth of protoplasts into callus and regeneration of shoots requires the proper balance of plant growth regulators in the tissue culture medium that must be customized for each species of plant. Unlike protoplasts from vascular plants, protoplasts from mosses, such as Physcomitrella patens, do not need phytohormones for regeneration, nor do they form a callus during regeneration. Instead, they regenerate directly into the filamentous protonema mimicking a germinating moss spore.
Protoplasts may also be used for plant breeding, using a technique called protoplast fusion. Protoplasts from different species are induced to fuse by using an electric field or a solution of polyethylene glycol. Originally, non–Ti-plasmid dependent DNA uptake was demonstrated in 1985 by R. Hain and A.P. Czernilofsky et al., in the article "Uptake, integration, expression and genetic transmission of a selectable chimaeric gene by plant protoplasts" using the Ca-phosphate coprecipitation technique. This technique may be used to generate somatic hybrids in tissue culture.
Additionally, protoplasts of plants expressing fluorescent proteins in certain cells maybe used for Fluorescence Activated Cell Sorting (FACS), where only cells fluorescing a chosen wavelength are retained. Among other things, this technique is used to isolate specific cell types (e.g. guard cells from leaves, pericycle cells from roots) for further investigation such as transcriptomics.
- Davey MR, Anthony P, Power JB, Lowe KC (March 2005). "Plant protoplasts: status and biotechnological perspectives". Biotechnol. Adv. 23 (2): 131–71. doi:10.1016/j.biotechadv.2004.09.008. PMID 15694124.
- Thorpe TA (October 2007). "History of plant tissue culture". Mol. Biotechnol. 37 (2): 169–80. doi:10.1007/s12033-007-0031-3. PMID 17914178.
- S.C. Bhatla, Justine Kiessling, Ralf Reski (2002): of polarity induction by cytochemical localization of phenylalkylamine-binding receptors in regenerating protoplasts of the moss Physcomitrella patens. Protoplasma 219, 99–105.
- R. Hain and A.P. Czernilofsky et al. (1985). "Uptake, integration, expression and genetic transmission of a selectable chimaeric gene by plant protoplasts". Mol Gen Genet 199:161–168.