New Method for Enhancing Coconut (Cocos nucifera L.) Embryo Dehydration: An Important Step Towards Proficient Cryopreservation
Amirhossein Bazrafshan | Sisunandar Sudarma | Sundaravelpandian Kalaipandian | Julianne M. Biddle | Zhihua Mu | Eveline Yee Yan Kong | Naga Prafulla Chandrika Nulu | Steve W. Adkins
The coconut (Cocos nucifera L.), a valuable tropical crop, is rapidly declining in genetic diversity due to natural disasters, pest and disease attack, and land clearing for other crops. Seed banking is impractical for coconut conservation due to its large, recalcitrant seed, and maintaining field gene bank collections is costly and vulnerable to environmental pressures. Cryopreservation offers a promising alternative method for conserving coconut genetic diversity, but the success in recovering cryopreserved materials remains limited, with few studies consistently reporting high rates of recovery. This highlights the need for improved cryopreservation protocols, particularly in tissue dehydration, which is one of the critical steps in the process of cryopreservation and plant recovery. A desiccator was developed that enabled rapid embryo dehydration with ultra-dry airflow. The desiccator reduced embryo moisture content to 20% (the predetermined viability threshold) within 6 h representing a 2-h improvement when compared to a previous dehydration approach, while maintaining a high germination rate (71%). Smaller embryos (500 to 550 mg fresh weight) desiccated faster than larger embryos (800 to 900 mg fresh weight) but germination was reduced (30%), making small embryos unsuitable for cryopreservation. A 5-day sucrose (0.4 M) pre-treatment further reduced the dehydration time to 4 h, while maintaining a high germination rate (70%). These advances in the use of a sucrose pre-treatment, the rapid embryo dehydration, and selection of large embryos size will help to enhance the success of coconut embryo cryopreservation and recovery.
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