|
Importance of structural integrity of somatic embryos for
long-term cryopreservation of cocoa (Theobroma cacao
L.) germplasm
Jong-Yi Fang1*
and Andy
Wetten2
1Department
of Tropical Agriculture and International Cooperation,
National Pingtung University of Science and Technology, No.1
Shueh Fu Road, Neipu, Pingtung 91201, Taiwan.
2School
of Biological Sciences, University of Reading, Whiteknights,
P.
O. Box 221,
Reading, Berkshire RG6 6AS, United Kingdom.
*Corresponding author. E-mail:
jongyifang@hotmail.com .
Accepted 11 May, 2011 |
|
 
Cryopreservation is a
reliable means for the long-term conservation of plant
genetic resources. It is of particular interest for cocoa (Theobroma
cacao L.) whose seeds are recalcitrant to conventional
storage methods and field collections susceptible to disease
infestations. However, the encapsulation- dehydration
procedure previously developed for cocoa somatic embryos has
resulted in poor survival after retrieval from liquid
nitrogen. To examine the causes of such failure, cocoa
somatic embryos following each treatment step of the
encapsulation-dehydration procedure were examined using a
combination of confocal scanning laser microscopy and
transmission electron microscopy. Results showed that the
parenchyma’s cells of the hypocotyl and radicle were the
major sites of injury possibly due to their large size and
non-cytoplasmic nature, whereas the shoot meristem and
provascular strand were well preserved throughout the
treatments. In general, cell deformation and/or disruption
was observed following the sucrose preculture, desiccation
and freezing steps, with the extent of damage increasing at
each treatment step. Post-thaw regrowth of injured embryos
was possible through the proliferation of surviving cells,
but these embryos often failed to convert into plantlets.
The present study suggests that the maintenance of
structural integrity of somatic embryos at each treatment
step is essential for the successful cryopreservation of
cocoa germplasm.
Key words:
Cocoa somatic embryos, confocal scanning laser microscopy,
cryopreservation, structural integrity, transmission
electron microscopy. |