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WHAT IS
MICROPROPAGATION?
Micropropagation is a propagation method that involves
the growth of plant tissues or cells in vitro. It is highly
efficient and can create a large number of plants from a
single specimen. The process involves carefully selected
tissue explants, which are sterilized and placed in
nutrient-rich media.
MEDIA FOR
MICROPROPAGATION
For micropropagation, MS-based media are widely
adopted. Generally they are supplemented with sucrose as
a carbon source at a concentration of 30-40 g/l.
media; 2,4-D,
2,4-dichlorophenoxyacetic acid;
BA, benzyl adenine
 NAA, α-naphthalene acetic acid
THE BENEFITS OF
MICROPROPAGATION
High Yield Potential
Micropropagation helps grow multiple copies
of the same plant in quick succession, which
boosts yields and maximizes production
efficiency.
Disease-Free Specimens
By starting with disease-free plant material,
growers can propagate new citrus specimens
without the risk of introducing diseases and
pests prevalent in the orchard.
Consistent Quality
The use of tissue culture techniques
ensures that every propagated plant
is identical in genetic makeup and
quality to the mother plant.
Shorter Maturation Time
Growers can shorten the maturation
time of new citrus plants by
manipulating plant growth
regulators, temperature, and light
conditions in the micropropagation
environment.
MICROPROPAGATION
PROCESS IN DETAIL
Source Plant Selection
Choose a healthy mother plant free of pests and
diseases. The plant should be at its growth peak,
and its tissues should be used as explants.
 Epicotyl
 Cotyledons
Root segments
Petiole
Leaf segments
 Shoot tip
 Meristem
 Explants Sterilization
 Explants are sterilized by immersion in a bleach solution, rinsed with
sterile water, and then treated with alcohol to prevent infections during in
vitro culture.
Explant Culture Initiation
The sterilized explants are placed in the in vitro culture
containing nutrient-rich media to initiate plant cell
growth and development.
In Vitro Plantlet Development
After explants have developed, microshoots or plantlets
successfully grown in vitro are removed and transferred to
larger glassware containing nutrient-rich media to
produce a larger number of plants.
LABORATORY
REQUIREMENTS FOR
MICROPROPAGATION
Clean Room
Laminar Air Flow
Chemicals & Reagents
Equipment
 From one to many propagules rapidly
Multiplication in controlled laboratorium conditions
Continuous propagation year round
 Potential for disease-free propagules
Specialized equipment/facilities required
More technical expertise required
Protocols not optimized for all species
Plants produced may not fit industry standards
citrus.pptx ent jvjvguzugfuffugcgchcyfhvhv

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citrus.pptx ent jvjvguzugfuffugcgchcyfhvhv

  • 1.
  • 2. WHAT IS MICROPROPAGATION? Micropropagation is a propagation method that involves the growth of plant tissues or cells in vitro. It is highly efficient and can create a large number of plants from a single specimen. The process involves carefully selected tissue explants, which are sterilized and placed in nutrient-rich media.
  • 3. MEDIA FOR MICROPROPAGATION For micropropagation, MS-based media are widely adopted. Generally they are supplemented with sucrose as a carbon source at a concentration of 30-40 g/l. media; 2,4-D, 2,4-dichlorophenoxyacetic acid; BA, benzyl adenine  NAA, α-naphthalene acetic acid
  • 4. THE BENEFITS OF MICROPROPAGATION High Yield Potential Micropropagation helps grow multiple copies of the same plant in quick succession, which boosts yields and maximizes production efficiency. Disease-Free Specimens By starting with disease-free plant material, growers can propagate new citrus specimens without the risk of introducing diseases and pests prevalent in the orchard.
  • 5. Consistent Quality The use of tissue culture techniques ensures that every propagated plant is identical in genetic makeup and quality to the mother plant. Shorter Maturation Time Growers can shorten the maturation time of new citrus plants by manipulating plant growth regulators, temperature, and light conditions in the micropropagation environment.
  • 6. MICROPROPAGATION PROCESS IN DETAIL Source Plant Selection Choose a healthy mother plant free of pests and diseases. The plant should be at its growth peak, and its tissues should be used as explants.
  • 9.  Shoot tip  Meristem  Explants Sterilization  Explants are sterilized by immersion in a bleach solution, rinsed with sterile water, and then treated with alcohol to prevent infections during in vitro culture.
  • 10. Explant Culture Initiation The sterilized explants are placed in the in vitro culture containing nutrient-rich media to initiate plant cell growth and development. In Vitro Plantlet Development After explants have developed, microshoots or plantlets successfully grown in vitro are removed and transferred to larger glassware containing nutrient-rich media to produce a larger number of plants.
  • 11. LABORATORY REQUIREMENTS FOR MICROPROPAGATION Clean Room Laminar Air Flow Chemicals & Reagents Equipment
  • 12.
  • 13.  From one to many propagules rapidly Multiplication in controlled laboratorium conditions Continuous propagation year round  Potential for disease-free propagules
  • 14. Specialized equipment/facilities required More technical expertise required Protocols not optimized for all species Plants produced may not fit industry standards