Asada-Halliwell pathway maintains redox status in Dioscorea alata tuber which helps in germination

Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Détails bibliographiques
Publié dans:Plant science : an international journal of experimental plant biology. - 1985. - 250(2016) vom: 15. Sept., Seite 20-29
Auteur principal: Sharma, Shruti (Auteur)
Autres auteurs: Sehrawat, Ankita, Deswal, Renu
Format: Article en ligne
Langue:English
Publié: 2016
Accès à la collection:Plant science : an international journal of experimental plant biology
Sujets:Journal Article Asada-Halliwell cycle Mature & germinating tuber Nitric oxide Reactive oxygen species S-nitrosothiol Biomarkers Plant Proteins Nitric Oxide 31C4KY9ESH plus... Glutathione GAN16C9B8O Ascorbic Acid PQ6CK8PD0R
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245 1 0 |a Asada-Halliwell pathway maintains redox status in Dioscorea alata tuber which helps in germination 
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520 |a Reactive Oxygen Species (ROS) are important regulatory molecules governing physiological processes. In the present study a biochemical and proteome level comparison of two contrasting growth stages of Dioscorea alata tuber namely germinating and mature tuber was performed in order to understand the tuber physiology and biochemistry. Existence of all the component enzymes [APx (ascorbate peroxidase), GR (glutathione reductase), DHAR (dehydroascorbate reductase), MDHAR (mono-dehydroascorbate reductase)] and major products [ascorbate (ASC) and glutathione (GSH)] of the cycle showed an operational Asada-Halliwell cycle in the tuber. A 2.65 fold increase in ASC content & a 3.8 fold increase in GR activity fortified the redox milieu during germination. In contrast a 5 fold higher H2O2 content (due to 3.08 fold lower APx activity) and accumulation of reactive nitrogen species (RNS) such as nitric oxide (NO, 2.4-fold) and S-nitrosothiol (SNO, 2.08 fold) contributed to overall oxidative conditions in the mature tuber. The carbonic anhydrase (CA, 7.5 fold), DHAR (5.31 fold) and MDHAR (7 fold) activities were higher in the germinating tuber in comparison with the mature tuber. GSNO negatively regulated the CA (3.6 & 3.95 fold), MDHAR (7.5 & 1.5 fold) and APx (2.3 & 1.81 fold) while another NO donor, CysNO negatively regulated the DHAR (2.24 & 1.32 fold) activity in the mature and germinating stages respectively indicating again that the lesser inhibition by NO (via nitrosylation) may be because of overall reducing environment in the germinating tuber. Increased SNO leading to S-nitrosylation of dioscorin was confirmed by Biotin switch assay. This is the first report showing dioscorin nitrosylation. The present analysis showed differential redox regulation and also suggests the physiological relevance of CA, DHAR, MDHAR, APx & GR in tuber germination for the first time. These enzymes may be used as potential markers of tuber germination in future 
650 4 |a Journal Article 
650 4 |a Asada-Halliwell cycle 
650 4 |a Mature & germinating tuber 
650 4 |a Nitric oxide 
650 4 |a Reactive oxygen species 
650 4 |a S-nitrosothiol 
650 7 |a Biomarkers  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a Nitric Oxide  |2 NLM 
650 7 |a 31C4KY9ESH  |2 NLM 
650 7 |a Glutathione  |2 NLM 
650 7 |a GAN16C9B8O  |2 NLM 
650 7 |a Ascorbic Acid  |2 NLM 
650 7 |a PQ6CK8PD0R  |2 NLM 
700 1 |a Sehrawat, Ankita  |e verfasserin  |4 aut 
700 1 |a Deswal, Renu  |e verfasserin  |4 aut 
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773 1 8 |g volume:250  |g year:2016  |g day:15  |g month:09  |g pages:20-29 
856 4 0 |u http://dx.doi.org/10.1016/j.plantsci.2016.05.013  |3 Volltext 
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