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Modification of reactive oxygen species scavenging capacity of chloroplasts through plastid transformation

  • Miranda Poage
  • , Bénédicte Le Martret
  • , Marcel A.K. Jansen
  • , Gregory D. Nugent
  • , Philip J. Dix
  • Midland College
  • Maynooth University
  • Royal Melbourne Institute of Technology University

Research output: Contribution to journalArticlepeer-review

Abstract

Reactive oxygen species (ROS), including superoxide anions, hydrogen peroxide and hydroxyl radicals are generated through normal biochemical processes, but their production is increased by abiotic stresses. The prospects for enhancing ROS scavenging, and hence stress tolerance, by direct gene expression in a vulnerable cell compartment, the chloroplast, have been explored in tobacco. Several plastid transformants were generated which contained either a Nicotiana mitochondrial superoxide dismutase (MnSOD) or an Escherichia coli glutathione reductase (gor) gene. MnSOD lines had a three-fold increase in MnSOD activity, but interestingly a five to nine-fold increase in total chloroplast SOD activity. Gor transgenic lines had up to 6 times higher GR activity and up to 8 times total glutathione levels compared to wild type tobacco. Photosynthetic capacity of transplastomic plants, as measured by chlorophyll content and variable fluorescence of PSII was equivalent to non-transformed plants. The response of these transplastomic lines to several applied stresses was examined. In a number of cases improved stress tolerance was observed. Examples include enhanced methyl viologen (Paraquat)-induced oxidative stress tolerance in Mn-superoxidase dismutase over-expressing plants, improved heavy metal tolerance in glutathione reductase expressing lines, and improved tolerance to UV-B radiation in both sets of plants.

Original languageEnglish
Pages (from-to)371-384
Number of pages14
JournalPlant Molecular Biology
Volume76
Issue number3-5
DOIs
Publication statusPublished - Jul 2011

Keywords

  • Abiotic stress
  • Chloroplast transformation
  • Glutathione reductase
  • Superoxide dismutase

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