Germplasm Conservation
1. Germplasm conservation refers to the conservation of living genetic resources like pollen, seeds or tissue of plant material maintained for the purpose of selective plant breeding, preservation in live condition and used for many research works.
2. Germplasm conservation resources is a part of collection of seeds and pollen that are stored in seed or pollen banks, so as to maintain their viability and fertility for any later use such as hybridization and crop improvement.
3. Germplasm conservation may also involve a gene bank, DNA bank of elite breeding lines of plant resources for the maintenance of biological diversity and also for food security.

Cryopreservation (- 195.C)
1. Cryopreservation, also known as Cryo conservation.
2. A process by which protoplasts, cells, tissues, organelles, organs, extracellular matrix, enzymes or any other biological materials are subjected to preservation by cooling to very low temperature of -196^oC using liquid nitrogen.
3. At this extreme low temperature any enzymatic or chemical activity of the biological material will be totally stopped and this leads to preservation of material in dormant status.
4. Later these materials can be activated by bringing to room temperature slowly for any experimental work.
5. Protective agents like dimethyl sulphoxide, glycerol or sucrose are added before cryopreservation Process.
6. These protective agents are called cryoprotectants, since they protect the cells, or tissues from the stress of freezing temperature.

Somatic embryogenesis is the formation of embryos from the callus tissue directly and these embryos are called Embryoids or from the in vitro cells directly form pre-embryonic cells which differentiate into embryoids
Applications:
i. Somatic embryogenesis provides potential plantlets which after hardening period can establish into plants.
ii. Somatic embryoids can be used for the production of synthetic seeds.
iii. Somatic embryogenesis is now reported in many plants such as Allium sativum, Hordeum vulgare, Oryza sativa, Zea mays and this is possible in any plant.

1. The growing of cells including the culture of single cells or small aggregates of cells in vitro in liquid medium is known as cell suspension culture.
2. The cell suspension is prepared by transferring a portion of callus to the liquid medium and agitated using rotary shaker instrument.
3. The cells are separated from the callus tissue and used for cell suspension culture.

Sterilization of Nutrient Media:
1. Culture media are dispensed in glass containers, plugged with non-absorbent cotton or sealed with plastic closures and then sterilized using autoclave at 15 psi (121^o(C)  for 15 to 30 minutes.
2. The plant extracts, vitamins, amino acids and hormones are sterilized by passing through Millipore filter with 0.2 mm pore diameter.
3. Then added to sterilized culture medium inside Laminar Airflow Chamber under sterile condition.
Other techniques used to remove the microbes
(a) Maintenance of aseptic environment
(b) Sterilization of culture room
(c) Sterilization of explants