Abstract

A comparison of the hydrogen peroxide (H2O2) content, proline and betacyanin concentration and activities of some antioxidant enzymes (catalase, superoxide dismutase, guaiacol and ascorbate peroxidases) was made in Mesembryanthemum crystallinum L. calli differing in rhizogenic potential. Callus was induced from hypocotyls of 10-day-old seedlings on a medium containing 1 mg l−1 2,4-dichlorophenoxyacetic acid and 0.2 mg l−1 kinetin, which was either supplemented with 40 mM NaCl (CIM-NaCl medium) or did not contain any salt (CIM medium). The callus obtained on CIM-NaCl was rhizogenic, whereas the callus induced on the medium without salt was non-rhizogenic throughout the culture. The rhizogenic callus differed from the non-rhizogenic callus in lower betacyanin and H2O2 content, but the rhizogenic callus displayed a higher proline level. The activity of H2O2 scavenging enzymes, such as catalase (CAT), ascorbate peroxidase (APX) and guaiacol peroxidase (POD), was markedly higher in the rhizogenic callus than in the non-rhizogenic callus, but the total activity of superoxide dismutase (SOD) was higher in the non-rhizogenic callus than in the rhizogenic callus. Aminotriazole (CAT inhibitor) and diethyldithiocarbamate (SOD inhibitor) were added solely to the CIM and CIM-NaCl media to manipulate the concentration of reactive oxygen species (ROS) in the cultured tissues. Both CAT and SOD inhibitors brought about an increase in H2O2 content in calli cultured on CIM-NaCl and the loss of rhizogenic potential. Conversely, the addition of inhibitors to the medium without salt led to a decrease in H2O2 content. This corresponded with a significant decrease in the endogenous concentration of betacyanins, but did not change the lack of rhizogenic ability.

Highlights

  • Reactive oxygen species (ROS) are known to be an intrinsic signal in plant development (Vranovaet al. 2002; Slesak et al 2007)

  • The results presented here revealed that rhizogenesis in the callus cells of M. crystallinum was dependent on NaCl addition to the growth medium

  • The reactive oxygen species (ROS) level and cellular redox potential might lead to the induction of genes responsible for regeneration processes in callus of M. crystallinum cultured on a medium supplemented with salt (CIM-NaCl)

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Summary

Introduction

Reactive oxygen species (ROS) are known to be an intrinsic signal in plant development (Vranovaet al. 2002; Slesak et al 2007). Reactive oxygen species (ROS) are known to be an intrinsic signal in plant development The level and type of ROS, e.g. superoxide radical (O2Á-), hydrogen peroxide (ÁH2O2) or hydroxyl radical (ÁOH), determine plant cell response. E.g. superoxide dismutase (SOD), peroxidase (POX) and catalase (CAT), are involved in the regulation of the ROS level. SOD (EC 1.15.1.1) is a metalloenzyme which plays a key role in protecting against ROS by converting the superoxide radical to hydrogen peroxide and oxygen. Catalase (EC 1.11.1.6) and peroxidases (EC 1.11.1.7) take part in the conversion of hydrogen peroxide to water and molecular oxygen. Guaiacol peroxidase (POD) participates in hydrogen peroxide removal during processes such as biosynthesis of lignin, plant development and organogenesis as well as senescence and responses to wounding and pathogens (Matamoros et al 2003)

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