Plant Tissue Culture
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Transcript Plant Tissue Culture
Plant Tissue Culture
Original by Linda Rist
Modified by Georgia Agricultural
Education Curriculum Office
July, 2002
T.C.
Refers to technique of
growing plant cells, tissues,
organs, seeds
or other plant parts in a
sterile environment on a
nutrient medium
History
In 1902 Haberlandt
proposed that single plant
cells could be cultured
Haberlandt
did not culture them
himself
1930’s
White worked on T.C.
discovery of plant growth
regulators
1930’s
importance of vitamins was
determined for shoot and root
culturing
1930’s
Indole-Acetic Acid
IAA
discovered in 1937
IAA
2,4-D
Dicamba
NAA
IBA
all synthetic hormones
1957-58
Miller and Skoog
University of Wisconsin Madison
discovered Kinetin
Kinetin
a cytokinin
plays active role in
organogenesis
1958
Steward developed somatic
embryo from carrot cells
1958-60
Morel cultured orchids and
dahlias
freed them from a viral
disease
1962
Murashige and Skoog
published recipe for MS
Medium
60’s & 70’s
Murashige cloned plants in
vitro
promoted development of
commercial plant T.C. labs
1966
raised haploid plants from
pollen grains
1972
used protoplast fusion to
hybridize 2 species of
tobacco into one plant
contained 4N
4N
all chromosomes of both
plants
70’s &80’s
develop techniques to
introduce foreign DNA into
plant cells
beginning of genetic
engineering
T.C. Media
functions
provide H2O
provide mineral nutritional
needs
T.C. Media
provide growth regulators
Provide vitamins
provide organic compounds
T.C. Media
provide access to
atmosphere for gas exchange
serve as a dumping ground
for plant metabolites
T.C. Media
H2O is usually distilled
minerals must provide 17
essential elements
energy source and carbon
skeletons - sucrose is
preferred
Vitamins
thiamine
pyridoxin
nicotinic acid
biotin
Vitamins
citric acid
ascorbic acid
inositol
Growth Regulators
auxins and cytokinins
gibberellic acid
abscissic acid
pH of media
usually 5.0-5.7
Media
must be sterile
autoclave at 250 F at 15 psi
for 15 minutes
T.C. Stages
Explanting- Stage I
get plant material in sterile
culture so it survives
provide with nutritional and
light needs for growth
Stage II
rapid multiplication
stabilized culture
goal for a commercial lab
difficult and time
consuming to maintain
Stage II
occurs in different
pathways in different plants
Rooting - Stage III
may occur in Stage II
usually induced by changes
in hormonal environment
lower cytokinin
concentration and increase
auxin
Rooting
may skip stage III and root
in a greenhouse
Stage IV
transplantation and
aftercare
usually done in greenhouse
keep RH high (relative
humidity)
Stage IV
gradually increase light
intensity and lower RH after
rooting occurs
allows plants to harden and
helps plants form cuticle
Cuticle
waxy substance promotes
development of stomates
plants in T.C. don’t have
cuticle
Explant
portion of plant removed
and used for T.C.
Important features
size
source - some tissues are
better than others
Explant
species dependent
physiological age - young
portions of plant are most
successful
Explant
degree of contamination
external infestation - soak
plant in sodium hypochlorite
solution
Explant
internal infection - isolate
cell that is not infected
roots - especially difficult
because of soil contact
Explant
herbaceous plants
soft stem
easier to culture than
woody plants
Patterns of
multiplication
stage II - light 100-300 foot
candles
callus - shoots - roots
stage III - rooting - light
intensity 1000-3000 foot
candles
Genetic
transformation
permanent incorporation of
new or foreign DNA into
genome of cell
Transformation
methods
protoplast fusion
cell wall is removed by
enzymes from cell
Protoplasts
naked plant cells
from 2 different plants can
be mixed together and forced
to fuse
Protoplast fusion
results in heterokaryon
cell containing two or more
nuclei from different cells
homokaryon - from same
cell
Protoplast fusion
allowed to regenerate cell
wall and then grow into
callus
callus turns to shoots
Shotgun approach
DNA coated micro bullets
of gold or tungston
shot into growing cells
DuPont holds the patent
Shotgun approach
injures cells
random success rate
PEG
Polyethylene glycol
pores open similar to
electroporation
Ti Plasmids
Tumor inducing
Agrobacterium
temefasciens
infect cells with
agrobacterium which
contains desired DNA
Ti Plasmids
monocots resist
agrobacterium infection
researchers are working to
overcome this
Luciferase
an enzyme
put into tobacco using Ti
plasmid
Luciferase
when transformed tobacco
plants are watered with
solution containing Luciferin
they break it down and emit
light
Luciferase
glowing in the dark
like a fire fly
Screening techniques
used to identify if culture
has taken on desired new
trait
Examples
sensitivity to antibiotics
color
sensitivity to excess
deficiencies of substances in
growth media
Conventional
plant breeding
egg cell gives half the
chromosomes and almost all
of the cytoplasm
male only gives its
chromosomes
Cont…….
This condition is called
maternal cytoplasmic
inheritance
Microinjection
single cells from culture are
held stationary with gentle
suction
injected with a tiny syringe
loaded with DNA
Microinjection
done under electron
microscope
Electroporation
desired DNA in solution
outside cell
high energy pulses - 50,000
volts
for a millisecond
Electroporation
cause tiny pores to open
allows DNA to enter the
cell