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Micrografting

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Micrografting (shoot tip grafting)

• The term micro grafting means the grafting of meristamatic tissues in vitro in the laboratory in
which the shoots of one plant are grafted on to the shoots or roots of another plant so as to
combine the characteristics of the two plants.
This method was used for the first time in 1952 by Morel and Martin . Micrografting was
initially used on vegetables. The success rate of micrografting is relatively high (80– 90%) for
tomatoes.
Micrografting consists of the placement in aseptic conditions of a maintained scion onto an in
vitro grown rootstock.
• The results of in vitro micrografting and the plant material derived from it can be further
multiplied in tissue culture conditions or acclimatized to outdoor conditions.
• Micrografting is a technique that potentially can combine the advantages of rapid in vitro
multiplication with increased productivity that results from grafting, superior rootstock and scion
combinations
. • Among various methods of micrografting, slit or wedge grafting has been found most suitable
in case of fruit crops.
• In vitro shoot tips are better as compared to in vivo shoot tips for carrying out micrografting
resulting in higher graft success, less contamination, lower shoot tip necrosis and good vigour of
micrografts.
This comprises the following steps
• Aseptic condition was maintained throughout all stages of micrografting process.
• Seedlings were removed carefully from the agar medium with sterilized forceps.
• For use as rootstock, seedlings were cut back to 1 cm above the cotyledonary nodes and leaves
were excised using a microscalpel.
• Terminal shoots to be used as scions were excised from the other seedlings at 2 cm below the
apex. • Lower leaves removed from the basal 1 cm of scion.
• Excised scion and rootstocks were stored in sterile de-ionized water until used in the grafting
process.
The shoot tip was inserted at the top of decapitated rootstock by making an incision.
• The cortex was exposed by the horizontal cut of the incision.
• Grafted plants were cultured in a liquid nutrient medium containing plant cell culture salt
solution of MS, modified White's vitamins and 75 g/1 sucrose.
• When at least two expanded leaves were formed micrografted plants were transferred to pots
containing a steam sterilized soil mixture suitable for plant.
Importance
• 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 plant

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