Cryopreservation of Brassidium Shooting Star Orchid Using the PVS3 Method Supported with Preliminary Histological Analysis

• Published in: Applied biochemistry and biotechnology 2014, Vol.172 (2), p.1131-1145
• Main Authors: Mubbarakh, Safiah Ahmad, Rahmah, Safrina, Rahman, Zuraida Abdul, Sah, Nazrin Nadirah Mohd, Subramaniam, Sreeramanan
• Format: Article
• Language: English
• Subjects: Biochemistry; Biological and medical sciences; Biotechnology; Chemistry; Chemistry and Materials Science; cryopreservation; Cryopreservation - methods; cytoplasm; Flowers & plants; Fundamental and applied biological sciences. Psychology; Genetic resources; glycerol; Histology; hybrids; nitrogen; Oncidium; Orchidaceae; Orchidaceae - anatomy & histology; Orchidaceae - cytology; Orchidaceae - drug effects; Orchidaceae - growth & development; Plant resources; Preservation; Resource conservation; sucrose; Sucrose - pharmacology; viability; vitrification; Vitrification - drug effects
• ISSN: 0273-2289; 1559-0291
• DOI: 10.1007/s12010-013-0597-0

Cryopreservation is an alternative, safe, and cost-effective method for long-term plant genetic resource conservation. This study was conducted to optimize the conditions for cryopreserving the protocorm-like bodies (PLBs) of Brassidium Shooting Star orchid with the PVS3 vitrification method. Five parameters were assessed in this study: PLB size, sucrose concentration, preculture duration, PVS3 duration, and unloading duration. The viability of the cryopreserved PLBs was determined using the triphenytetrazolium chloride assay and growth recovery assessments. The optimum condition for the cryopreservation of the PLBs of Brassidium Shooting Star orchid is based on the size range between 3 and 4 mm precultured with half-strength semi-solid MS media supplemented with 0.25 M sucrose for 24 h, followed by treatment with loading solution mixture of 2 M glycerol and 0.4 M sucrose supplemented with half-strength liquid MS media at 25 °C for 20 min. The PLBs were then dehydrated with PVS3 at 0 °C for 20 min prior to immersion in liquid nitrogen; finally, the PLBs were immersed with half-strength liquid MS media supplemented with 1.2 M sucrose for 30 min. Histological analyses displayed denser cytoplasm and voluminous nucleus in the cryopreserved PLBs of Brassidium Shooting Star orchid.