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Plant Tissue Culture

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Technical Course

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Page 1: Technical Course

Plant Tissue Culture

Page 2: Technical Course

T.C. Refers to technique of growing

plant cells, tissues, organs, seedsor other plant parts in a sterile

environment on a nutrient medium

Page 3: Technical Course

HistoryIn 1902 Haberlandt

proposed that single plant cells could be cultured

Page 4: Technical Course

Haberlandtdid not culture them himself

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1930’sWhite worked on T.C.discovery of plant growth

regulators

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1930’simportance of vitamins was

determined for shoot and root culturing

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1930’sIndole-Acetic AcidIAAdiscovered in 1937

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IAA2,4-DDicambaNAAIBAall synthetic hormones

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1957-58Miller and SkoogUniversity of Wisconsin -

Madisondiscovered Kinetin

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Kinetina cytokininplays active role in

organogenesis

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1958Steward developed somatic

embryo from carrot cells

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1958-60Morel cultured orchids and

dahliasfreed them from a viral

disease

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1962Murashige and Skoogpublished recipe for MS

Medium

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60’s & 70’sMurashige cloned plants in

vitropromoted development of

commercial plant T.C. labs

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1966raised haploid plants from

pollen grains

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1972used protoplast fusion to

hybridize 2 species of tobacco into one plant

contained 4N

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4Nall chromosomes of both

plants

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70’s &80’sdevelop techniques to

introduce foreign DNA into plant cells

beginning of genetic engineering

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T.C. Mediafunctionsprovide H2Oprovide mineral nutritional

needs

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T.C. Mediaprovide growth regulatorsProvide vitaminsprovide organic compounds

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T.C. Mediaprovide access to

atmosphere for gas exchangeserve as a dumping ground

for plant metabolites

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T.C. MediaH2O is usually distilledminerals must provide 17

essential elementsenergy source and carbon

skeletons - sucrose is preferred

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Vitaminsthiaminepyridoxinnicotinic acidbiotin

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Vitaminscitric acidascorbic acidinositol

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Growth Regulatorsauxins and cytokininsgibberellic acidabscissic acid

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pH of mediausually 5.0-5.7

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Mediamust be sterileautoclave at 250 F at 15 psi

for 15 minutes

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T.C. StagesExplanting- Stage Iget plant material in sterile

culture so it survivesprovide with nutritional and

light needs for growth

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Stage IIrapid multiplicationstabilized culturegoal for a commercial labdifficult and time consuming

to maintain

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Stage IIoccurs in different pathways

in different plants

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Rooting - Stage IIImay occur in Stage IIusually induced by changes in

hormonal environmentlower cytokinin concentration

and increase auxin

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Rootingmay skip stage III and root

in a greenhouse

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Stage IVtransplantation and aftercareusually done in greenhousekeep RH high (relative

humidity)

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Stage IVgradually increase light

intensity and lower RH after rooting occurs

allows plants to harden and helps plants form cuticle

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Cuticlewaxy substance promotes

development of stomatesplants in T.C. don’t have

cuticle

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Explantportion of plant removed and used

for T.C.Important featuressizesource - some tissues are better

than others

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Explantspecies dependentphysiological age - young

portions of plant are most successful

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Explantdegree of contaminationexternal infestation - soak

plant in sodium hypochlorite solution

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Explantinternal infection - isolate

cell that is not infectedroots - especially difficult

because of soil contact

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Explantherbaceous plantssoft stemeasier to culture than woody

plants

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Patterns of multiplication

stage II - light 100-300 foot candles

callus - shoots - rootsstage III - rooting - light

intensity 1000-3000 foot candles

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Genetic transformation

permanent incorporation of new or foreigh DNA into genome of cell

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Transformation methods

protoplast fusioncell wall is enzymatically

removed from cell

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Protoplastsnaked plant cellsfrom 2 different plants can

be mixed together and forced to fuse

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Protoplast fusionresults in heterokaryon cell containing two or more

nuclei from different cellshomokaryon - from same

cell

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Protoplast fusionallowed to regenerate cell

wall and then grow into callus

callus turns to shoots

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Shotgun approachDNA coated micro bullets of

gold or tungstonshot into growing cellsDuPont holds the patent

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Shotgun approachinjures cellsrandom success rate

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PEGPolyethylene glycolpores open similar to

electroporation

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Ti PlasmidsTumor inducingAgrobacterium temefasciensinfect cells with

agrobacterium which contains desired DNA

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Ti Plasmidsmonocots resist

agrobacterium infectionresearchers are working to

overcome this

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Luciferasean enzyme put into tobacco using Ti

plasmid

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Luciferasewhen transformed tobacco

plants are watered with solution containing Luciferin

they break it down and emit light

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Luciferaseglowing in the darklike a fire fly

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Screening techniquesused to identify if culture

has taken on desired new trait

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Examplessensitivity to antibioticscolorsensitivity to excess

deficiencies of substances in growth media

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Conventional plant breedingegg cell gives half the

chromosomes and almost all of the cytoplasm

male only gives its chromosomes

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Cont…….This condition is called

maternal cytoplasmic inheritance

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Microinjectionsingle cells from culture are

held stationary with gentle suction

injected with a tiny syringe loaded with DNA

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Microinjectiondone under electron

microscope

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Electroporationdesired DNA in solution

outside cellhigh energy pulses - 50,000

voltsfor a millisecond

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Electroporationcause tiny pores to openallows DNA to enter the cell