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H E A L T H Y P L A N T S A N D M IC R O P R O P A G A T IO N

MICROCLONALPROPAGATIONOFVINE

A.O.Marchenko,M.A.Kostik

Institutefo r Vine and Wine "Magarach" 31, Kirov St., Yalta, 334200, UKRAINE, E-

Mail:

elena@magarach.crimea.ua;

"Ampelos", 24/14Mukhin St., Yalta, 334203,

UKRAINE

Commercial m icroclonal propagation o f vine is hampered by difficult

adaptation o f

in vitro

plants and high prime cost o f root ings obtained.

Approaches to improve efficiency of microclonal propagation were developed

based on ten cultivars and hybrid forms o f vine.

Microclonalpropagation.

A method of

in vitro

vegetative propagation by

single-bud cuttings was employed using techniques allowing to grow up to

400

in vitro

plants per 1 l o f nutrient medium, to obtain up to 20 nodes per

each

in vitro

plant, to produce plants with a good root system and resistance

to abrupt changes in hum idity and to conduct adaptation in several cycles.

Conditions for

in vitro

cultivation of plants during one year without transfers

to new media were determined to establish an

in vitro

collection o f valuable

cultivars and forms of vine.

Adaptation o f in vitro plants.

Preadaptation was based on the method

o f adaptation in culture vessels developed by A.B.Burgutin (Inst.Plant

Physiol., Moscow). The second stage o f adaptation was in open canals on

ceolite under a plastic film , providing irrigation with a nutrient solution. 20

days later the plastic film was removed and the plants were grown in the

open. If planting fo r adaptation took place prior to mid-May, normal rootings

were obtained,with an average increase growth o f 3 m.

The technology developed eliminates the problem of plant survival (even

if 30%) during adaptation: based on 1,000

in vitro

plants available in February,

fo u r adaptation cycles can be done prior to 1st June, yielding a total of

10,000 and more

in vitro

plants to be planted fo r adaptation; taking into

account losses o f 50% and varietal peculiarities, more than 400 adapted

plants can be produced during 8 months from each bud established in culture;

and rooting prime cost can be reduced to maximum 10% o f purchasing

price. The total efficiency o f the technology can be further improved by the

use o f efficient techniques o f microclonal propagation.

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