Abstract

Throughout the cryopreservation process, plants were exposed to a series of abiotic stresses such as desiccation and osmotic pressure due to highly concentrated vitrification solution. Abiotic stress stimulates the production of reactive oxygen species (ROS) which include hydrogen peroxide, superoxide radicals, and singlet oxygen. Higher production of ROS may lead to oxidative stress which contributes to the major injuries in cryopreserved explants. Antioxidant enzymes in plant such as ascorbate peroxidase (APX) can protect plants from cell damage by scavenging the free radicals. This study was determined based on APX enzyme activity of Aranda Broga Blue orchid's protocorm-like bodies (PLBs) in response to PVS2 (Plant Vitrification Solution 2) cryopreservation treatments at different stages. PLBs that were precultured at 0.25 M sucrose for 3 days were subjected to vitrification cryopreservation method. Results obtained showed that the highest APX activity was achieved at PVS2 cryoprotectant treatment prior liquid nitrogen (LN) storage. This phenomenon indicating that accumulation of osmotic and dehydrating stress throughout the cryopreservation treatment resulted in oxidative burst which in turn leads to higher APX activity in order to control the excess production of ROS. To conclude, PVS2 treatment was revealed as the most detrimental step throughout cryopreservation treatment. Thus, this research also suggested that exogenous antioxidant such as ascorbic acid can be added throughout cryopreservation procedure especially at PVS2 treatment in the future experiments to aid in regrowth of cryopreserved explants by reducing oxidative stress.

Highlights

  • When plants were exposed to abiotic and biotic stresses, reactive oxygen species (ROS) generation were triggered due to the activation of plant defence responses

  • To encounter oxidative damage caused by ROS, several antioxidant enzymes in the detoxification system are required to work in synchrony and ascorbate peroxidase (APX) is known to be the main antioxidant enzymes to detoxify hydrogen peroxides (Noctor & Foyer 1998)

  • The similar finding was obtained by Rahmah et al (2015) during cryopreservation of Brassidium Shooting Star orchid, where the APX activity increased from preculture until PVS2 dehydration and liquid nitrogen (LN) storage stages

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Summary

Introduction

When plants were exposed to abiotic and biotic stresses, ROS (reactive oxygen species) generation were triggered due to the activation of plant defence responses. Overproduction of ROS such as superoxide radicals may cause oxidation and damages to the plant cells. To overcome this phenomenon, plants are able to detoxify the harmful ROS with a series of antioxidant enzyme mechanism. APX in conjunction with glutathione reductase in the glutathione-ascorbate cycle are responsible in keeping the ROS activity in plant cells under control. Cryopreservation treatments impose the plants to a series of oxidative burst caused by freezing temperature and high osmotic stress. The objective of this study is to evaluate the oxidative level of PLBs using APX enzyme as stress marker at various cryopreservation stages

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