Eriksson’s Medium in Plant Tissue Culture: Origins, Uses, and Formulation
Eriksson’s medium, while less widely known than Murashige and Skoog (MS) or Gamborg’s B5 media, holds a significant place in the history of plant tissue culture. Its unique formulation makes it a valuable tool for specific applications, particularly within certain plant families. This article explores its origins, applications, formulation, and relevance in modern plant biotechnology.
Origin:
Developed by Torsten Eriksson and colleagues in the late 1960s and early 1970s, Eriksson’s medium wasn’t designed as a universal solution like MS medium. Instead, it emerged from research focused on improving the propagation and regeneration of woody plants, a group notoriously challenging to cultivate in vitro. The specific challenge Eriksson’s team addressed was overcoming the recalcitrance of certain woody species to efficient shoot multiplication and rooting in tissue culture. The medium aimed to provide a balanced nutrient environment conducive to the specific physiological requirements of these often recalcitrant plant species. While the exact publication year of the original formulation is not consistently cited, its usage and adaptations have been documented in multiple research papers since its inception.
Applications:
Eriksson’s medium found its niche in the cultivation of several plant families, particularly those known for difficulties in in vitro propagation. It shows particular success in the following areas:
Woody plant propagation: This remains its primary application. The medium is favored for micropropagation (cloning), shoot multiplication, and root induction in species from families like Acer (maples), Betula (birches), and Populus (poplars). The efficacy likely stems from its nutrient balance, potentially offering superior levels of specific macronutrients crucial for growth and differentiation in these species.
Orchids: Numerous studies report successful use of Eriksson’s medium (often with modifications) for orchid propagation, particularly for protocorm development and subsequent plantlet formation. Its suitability relates to the provision of a specific balance of nutrients and growth regulators optimal for orchid development stages.
- Other Applications: While less frequently used for other purposes, Eriksson’s medium has found application in callus induction and somatic embryogenesis in certain species, highlighting its adaptability to different in vitro processes. However, these are less common than its use in propagation.
Formulation:
A precise, universally agreed-upon formulation for Eriksson’s medium is difficult to pinpoint. Researchers often adapt the original components and concentrations based on the specific requirements of the target plant species. However, a representative composition is shown below. Note that concentrations may vary depending on the research publication. Units are given as mg/L unless otherwise stated.
Component | Concentration (mg/L) | Role |
---|---|---|
NH₄NO₃ | 1650 | Primary nitrogen source |
KNO₃ | 1900 | Nitrate source; Potassium source |
CaCl₂·2H₂O | 440 | Calcium source |
MgSO₄·7H₂O | 370 | Magnesium source |
KH₂PO₄ | 170 | Phosphate source |
FeSO₄·7H₂O | 27.8 | Iron source |
MnSO₄·H₂O | 2.2 | Manganese source |
ZnSO₄·7H₂O | 0.83 | Zinc source |
KI | 0.83 | Iodine source |
CuSO₄·5H₂O | 0.025 | Copper source |
Na₂MoO₄·2H₂O | 0.25 | Molybdenum source |
H₃BO₃ | 6.2 | Boron source |
EDTA | 37.3 | Chelating agent for micronutrients |
Thiamine-HCl | 1 | Vitamin B1 |
Pyridoxine-HCl | 1 | Vitamin B6 |
Nicotinic acid | 1 | Vitamin B3 |
Myo-inositol | 100 | Growth factor |
Sucrose | 30000 | Carbohydrate source |
Agar | 8000 | Solidifying agent |
Growth Regulators: The key to success with Eriksson’s medium often lies in the careful selection and adjustment of plant growth regulators (PGRs). Auxins (e.g., NAA, IBA) and cytokinins (e.g., BAP, kinetin) are commonly added at concentrations tailored to the specific requirements of the plant species and the desired phase of development (callus induction, shoot proliferation, rooting).
Conclusion:
Eriksson’s medium, while not as ubiquitous as MS or B5, retains relevance in plant tissue culture. Its strengths lie in its demonstrated effectiveness for recalcitrant woody plants and orchids, often outperforming other media in these particular applications. However, a limitation is its less standardized formulation, requiring careful optimization for each target species. Compared to MS medium, which is known for its broad applicability but can be less effective for specific challenging species, Eriksson’s medium provides a specialized alternative. B5 medium, while also versatile, often differs in its macronutrient balance and sometimes requires optimization to match the growth needs of recalcitrant plants. In summary, Eriksson’s medium continues to offer valuable opportunities where its specific characteristics provide a developmental advantage in plant tissue culture. Further research into medium optimization and the plant physiological responses to its unique composition continue to enhance its application in modern plant biotechnology.