Plant Tissue Culture What is Plant Tissue Culture

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Plant Tissue Culture

Plant Tissue Culture

What is Plant Tissue Culture? Tissue culture is the culture and maintenance of plant

What is Plant Tissue Culture? Tissue culture is the culture and maintenance of plant cells, tissues or organs (explants) in sterile, nutritionally (synthetic media) and environmentally (controlled) supportive conditions (in vitro).

What conditions do plant cells need to multiply in vitro? • Freedom from competition

What conditions do plant cells need to multiply in vitro? • Freedom from competition • Nutrients and removal of waste products • A controlled environment

Why Tissue Culture?

Why Tissue Culture?

Seed culture • Increasing efficiency of germination of seeds that are difficult to germinate

Seed culture • Increasing efficiency of germination of seeds that are difficult to germinate in vivo • Precocious germination by application of plant growth regulators • Production of clean seedlings for explants or meristem culture

Embryo culture • Overcoming embryo abortion due to incompatibility barriers • Overcoming seed dormancy

Embryo culture • Overcoming embryo abortion due to incompatibility barriers • Overcoming seed dormancy and self-sterility of seeds • Embryo rescue in distant (interspecific or intergeneric) hybridization where endosperm development is poor • Shortening of breeding cycle

Ovary or ovule culture • Production of haploid plants • A common explant for

Ovary or ovule culture • Production of haploid plants • A common explant for the initiation of somatic embryogenic cultures • Overcoming abortion of embryos of wide hybrids at very early stages of development due to incompatibility barriers • In vitro fertilization for the production of distant hybrids avoiding style and stigmatic incompatibility that inhibits pollen germination and pollen tube growth

Anther and microspore culture • Production of haploid plants • Production of homozygous diploid

Anther and microspore culture • Production of haploid plants • Production of homozygous diploid lines through chromosome doubling, thus reducing the time required to produce inbred lines • Uncovering mutations or recessive phenotypes

In vitro pollination • Production of hybrids difficult to produce by embryo rescue

In vitro pollination • Production of hybrids difficult to produce by embryo rescue

Organ culture • Any plant organ can serve as an explant to initiate cultures

Organ culture • Any plant organ can serve as an explant to initiate cultures

Shoot apical meristem culture • Production of virus free germplasm • Mass production of

Shoot apical meristem culture • Production of virus free germplasm • Mass production of desirable genotypes • Facilitation of exchange between locations (production of clean material) • Cryopreservation (cold storage) or in vitro conservation of germplasm

Somatic embryogenesis • • One major path of regeneration Mass multiplication Production of artificial

Somatic embryogenesis • • One major path of regeneration Mass multiplication Production of artificial seeds As source material for embryogenic protoplasts • Amenable to mechanization and for bioreactors

Organogenesis • One major path of regeneration • Mass multiplication • Conservation of germplasm

Organogenesis • One major path of regeneration • Mass multiplication • Conservation of germplasm at either normal or sub-zero temperatures

Enhanced axillary budding • Micropropagation

Enhanced axillary budding • Micropropagation

Callus Cultures • In some instances it is necessary to go through a callus

Callus Cultures • In some instances it is necessary to go through a callus phase prior to regeneration via somatic embryogenesis or organogenesis • For generation of useful somaclonal variants (genetic or epigenetic) • As a source of protoplasts and suspension cultures • For production of metabolites • Used in in vitro selection

In vitro mutagenesis • Induction of polyploidy • Introduction of genetic variability

In vitro mutagenesis • Induction of polyploidy • Introduction of genetic variability

Protoplast isolation, culture and fusion • Combining genomes to produce somatic hybrids, asymmetric hybrids

Protoplast isolation, culture and fusion • Combining genomes to produce somatic hybrids, asymmetric hybrids or cybrids • Production of organelle recombinants • Transfer of cytoplasmic male sterility

In vitro flowering • This can be done in some instances but I am

In vitro flowering • This can be done in some instances but I am not sure there any practical applications

Micrografting • Overcoming graft incompatibility • Rapid mass propagation of elite scions by grafting

Micrografting • Overcoming graft incompatibility • Rapid mass propagation of elite scions by grafting onto rootstocks that have desirable traits like resistance to soil-borne pathogens and diseases • To allow survival of difficult to root shoots • Development of virus free plants

Genetic transformation • Many different explants can be used, depending on the plant species

Genetic transformation • Many different explants can be used, depending on the plant species and its favored method of regeneration as well as the method of transformation • Introduction of foreign DNA to generate novel (and typically desirable) genetic combinations • Used to study the function of genes

Development of pre-existing structures Axillary bud De novo formation based on totipotentiality Adventitious bud

Development of pre-existing structures Axillary bud De novo formation based on totipotentiality Adventitious bud

Tuberization Flowering in vitro

Tuberization Flowering in vitro

Ovary development Rhizogenesis

Ovary development Rhizogenesis

Grafting in vitro Bulbil development

Grafting in vitro Bulbil development

Embryogenesis

Embryogenesis

Somatic embiryogenesis in cotton

Somatic embiryogenesis in cotton

History of plant tissue culture • • TOTİPOTENSİ Cell theory SCHLEIDEN 1838 in plants,

History of plant tissue culture • • TOTİPOTENSİ Cell theory SCHLEIDEN 1838 in plants, SCHWANN 1839 in plants and animals Among the lower plants any cell can be separated from the plant and continue to grow. Thus, entire plants may consist of cells whose capacity for independent life can be clearly demonstrated.

Haberland, 1902 (first aseptically culture attemp in a nutrient solution

Haberland, 1902 (first aseptically culture attemp in a nutrient solution

White, 1934 First root culture

White, 1934 First root culture

The in vitro cultivation of plant tissues for indefinite periods of time was simultaneously

The in vitro cultivation of plant tissues for indefinite periods of time was simultaneously achieved by WHITE working with a Nicotiana hybrid and GAUTHERET and NOBECOURT working with carrot Daucus carota in 1939. This achievement in both cases was due to a fortunate choice of plant material as both are considered to be relatively easy to culture now in comparison with many other species but this in no way negates the magnitude of their efforts.

Gautheret, first callus culture

Gautheret, first callus culture

Skoog, 1954

Skoog, 1954

Murashige • Murashige ve Skoog medium

Murashige • Murashige ve Skoog medium

Maheswari, 1960 first anther culture

Maheswari, 1960 first anther culture

Nitsch, 1974 microspore culture

Nitsch, 1974 microspore culture

Cocking, 1960 Protoplast culture •

Cocking, 1960 Protoplast culture •

Morel, 1960 micropropagation Melchers, 1978 protoplast fusion Pomato

Morel, 1960 micropropagation Melchers, 1978 protoplast fusion Pomato

Nickell, Sekondary metabolite production

Nickell, Sekondary metabolite production

Plant tissue culture studies in TURKEY • First at Agricultural Resarch Institions and Universities

Plant tissue culture studies in TURKEY • First at Agricultural Resarch Institions and Universities with micropropagation studies • Aegean and Ankara Universities and Bornova Agricultural Resarch Instition are pioneering • Today more than 30 Universities, Rsearch Institions, TÜBİTAK and private sector has tissue culture facilities.

* G r o w t h c h a m * laminar flows

* G r o w t h c h a m * laminar flows