Plant tissue and cell culture refers to the sterile growth and multiplication of plant cells, tissues, and organs in vitro, providing an efficient method for the propagation of plants under controlled conditions. By culturing plant cells with nutrient media in an artificial environment, it is possible to clonally propagate plants at scale, producing mature, disease-free specimens in a fraction of the time compared to traditional methods. This technique allows for the rapid generation of high-quality, uniform planting materials, which are invaluable for applications in molecular genetic engineering, plant breeding, horticultural production, and environmental conservation. Furthermore, plant tissue culture is also widely used in plant science, phycology, and pharmaceutical research. Common plant cell culture processes, such as seed culture, meristem culture, callus culture, and bud culture, typically involve placing tissues on a gel substrate, such as Murashige and Skoog (MS) media or Gamborg B5 medium. In some cases, plant tissues are grown in liquid media, as seen in cell suspension cultures. The formulation of plant culture media is tailored to the specific needs of the plant and typically includes macronutrients, micronutrients, vitamins, amino acids, nitrogen supplements, plant growth hormones, and plant growth regulators (PGRs). Advances in bioengineering and plant science have significantly improved the efficiency and outcomes of plant tissue and cell culture processes, opening new possibilities for plant research and cultivation.
Microbial contamination can be introduced at every stage of the tissue culture process, which may impose disastrous effects on crucial species conservation efforts. Meticulous tissue culture techniques are used with endangered, threatened, and rare plant species to quickly reproduce materials with a high coefficient of multiplication and rapid expansion from limited initial plant samples. Pathogen screening can prevent significant losses in micropropagation systems, enhancing production efficiency and improving output quality for conservation efforts. Plant tissue culture media that incorporates pathogen screening can help to diagnose, treat, or prevent future contamination, and facilitate faster production of mature and disease-free plants.
Plant secondary metabolites are made up of complex phytochemical components that provide protective or non-essential functions to plants, but may be of significant medicinal value to humans. When applied at the ideal stage of development, elicitors such as plant growth regulators (PGRs) can support cell growth and trigger secondary metabolic pathways that stimulate plant regulatory responses in phenolic and flavonoid synthesis. Plant-derived products such as flavors, fragrances, alkaloids, pigments and pharmaceuticals are of considerable value. Plant tissue culture techniques can support a cost-effective, sustainable, and controlled means of production of these products, time to market and expedite commercial applications.
Plant tissue culture techniques can be used in plant breeding efforts to meet growing global food demands. Protoplast isolation and culture allows plant breeders to overcome the challenges of traditional breeding and to facilitate gene transfer that permits testing for desirable characteristics. Protoplasts are cells which lack cell walls and can be used in plant tissue culture systems to regenerate whole plants from a single cell. Crop improvement efforts to increase quality, quantity and efficiency for agricultural crop production can achieve desired hybrids using protoplast fusion, isolation and culture despite incompatibility issues in traditional plant breeding.