

TO T IPO T EN C Y AND M O R PH O G E N E SIS O F PLANT C E L L S
IN V IT R O
OVERCOMINGGENOTYPEINFLUENCEONCUCUMBERPROTOPLAST
CULTURE
V.P.Duplij, A.V.Lytovchenko, V.A.Sidorov
Institute o fC ellBiology andGenetic EngineeringNatl. Acad. Sci. o fthe Ukraine
Zabolotnogo 148,252143Kiev, the UkraineEmail:
Janyk@PlantCells.Kiev.UATwenty years o f investigations carried out in the world have resulted
plant regeneration fo r a few cucumber (Cucumis sativus L ) genotypes only.
One can meet problems in the induction o f cell divisions and more often in
the stage o f obtaining whole plants.
In ou rwork mesophyll protoplast plating efficiency (PE) appeared to be
genotype dependent under conditions o f liquid culture medium and ranged
from 8 to 60%. PE was higher (8290%) fo r immobilized in Ca2+-alginate
protoplasts and the differences fo r various cucumber lines were statistically
indistinguishable. Somatic embryogenesis was induced fo r 5 gynoecious
lines only. Embryos o f 3 cucumber lines had a strong tendency to
dedifferentiation and secondary embryogenesis on the solid hormone free
MS medium but adding 0.1 mg/l ABA and 0.3-1 mg/l kinetin improved embryo
maturation and precipitated the whole plant obtaining. In the liquid MS medium
the phenomenon o f secondary embryogenesis was not observed but somatic
proembryos formed roots only, and it was necessary to stabilize culture
medium pH by 5 mM MES to obtain piantlels. A fte r 4-12 weeks from the
beginning of embryo maturation regenerants became morphologically sim ilar
to the plants grown
in vitro
from seeds.
This results allowed us to hope that protoplast culture conditions control
w ill make possible plant regeneration fo r more w ide range o f cucumber
genotypes.
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