Essay On Tissue Culture

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Tissue culture has been in practice since the early 1900’s. Since its start, there has been many breakthroughs in producing a viable plant from culture. Tissue culture is defined as the growth of plants from plant tissue in an artificial medium and a sterile environment. The uses for this technique include food processing, agriculture, pharmaceutics, and medicines. It has an influence on human welfare like food processing, human health, and environmental protection. There is an increasing demand for tissue culture, therefore it is becoming more popular exploring more of its commercial potential. Tissue culture is also used for production of pathogen free plants, germplasm preservations, and year round propagation.
Callus culture - Callus formation is a mass of undifferentiated cells from an explant. Both auxins and cytokinins are needed for proper development. Subculturing must be done every 3-5 weeks. This type of culture is mostly done for maintaining cell lines or morphogenesis.

Suspension culture - Cells are cultured in a liquid medium to form a callus. Subculturing needs to be done every 3-14 days due to their faster rate of growth than callus culture. This is the most used method in large scale production.

Single cell culture - Single cell culture produces a clone of identical cells through in vitro conditions. Pieces of a leave are macerated in a mortar and pestle with a buffer, then spun in a centrifuge. Cells are then cultured on a nurse medium.

Micropropagation - This method uses a mature cell to dedifferentiate into callus tissue. The two processes in micropropagation are known as organogenesis and somatic embryogenesis. Organogenesis develops shoot buds into apical meristems, while somatic embryogenesis forms non z...

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...then disinfected in a 10% bleach solution for 15 minutes. It is important to put all necessary materials needed for culturing in the laminar flow hood to prevent spreading contaminants once you begin working. After thoroughly washing your hands and arms, remove the leaf from the bleach solution with sterile forceps, then re-sterilize forceps and scalpel before cutting the petiole into 1cm pieces and the leaf into approximately 2cm squares. Place the explants on a petri dish with media, gently pressing to ensure contact between explant and media. First the explants are placed on an initiation medium, then later placed on a development medium. The medium used depends on the the stage of growth and requirements for salts, sugar, nutrients, vitamins, hormones, and pH. This process eventually produces many plantlets that can be transplanted into a non-sterile environment.

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