ABSTRACT
The Himalayan mulberry, Morus laevigata Wall. ex Brandis, is a cold tolerant species found commonly in India from Himalayan foothill to Andaman islands, and it is known for its timber value, forage use, particularly as silkworm's feed. Preservation of germplasm, cryopreservation, particularly for long term storage, of such economically important plant species helps in breeding and development of new cultivars. In the present study, three cryotechniques viz., two-step freezing, encapsulation-dehydration and vitrification were attempted for cryopreservation of of M. laevigata using winter dormant buds as explants. A two-step freezing cryo procedure preceded by desiccation to 15-25% moisture content was developed. Recovery conditions, including dark incubation and rehydration in sterile moist moss grass for different durations, after cryopreservation led to higher survival when compared to untreated controls. For encapsulation-dehydration, alginate beads containing descaled buds were dehydrated for 1-3 days in various sucrose concentrations (0.3, 0.5, 0.75 or 1.0 M). Bead desiccation was performed using laminar air flow for either 1-6 h. For vitrification, descaled buds were directly immersed for 20, 40, 60, 90 or 120 min in a vitrification solution (PVS2). Following encapsulation-dehydration, treatment of alginate beads with 0.75 M sucrose was more effective in promoting regrowth of explants after immersion in liquid nitrogen than in the presence of 0.75 M sucrose for 48 h. Regrowth of explants was also observed following vitrification which reached 50% with increasing duration of the PVS2 treatment for 20-90 min. Overall, the highest frequency of explant regrowth was obtained when explants were subjected to encapsulation-dehydration. This is possibly the first attempt for cryopreservation of Himalayan mulberry adopting these three new cryotechniques.
ABSTRACT
An efficient in vitro protocol was standardized for Almond (Prunus dulcis) propagation using dormant axillary buds as explants. Explants were cultured on Murashige and Skoog (MS) and woody plant medium (WPM) supplemented with different concentration/combination(s) of phytohormones. MS basal medium showed lowest shoot induction and took longest duration for shoot initiation. Multiple shoots were induced in MS medium supplemented with the combination of BAP (0.5 mgL-1). Cultures showed poor response for rooting in all combinations of plant growth regulators (PGRs) and took 90 days for initiation. Rooting was higher in half strength of MS than in full-strength. The highest root induction (33.33%) was recorded in half MS medium supplemented with 0.1 mgL-1 IBA (indole-3-butyric acid) followed by full strength of MS medium (20%) supplemented with IBA (0.1 mgL-1). α-Naphthalene acetic acid (NAA) was less effective for rooting than IBA. The highest root induction (25%) was found in half strength of MS medium supplemented with 0.1 mgL-1 NAA followed by full strength of MS medium (20%). The protocol developed would be of use in mass propagation of almond and also support in vitro conservation.