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2,4-dichlorophenoxyacetic acid-induced leaf senescence in mung bean (Vigna radiata L. Wilczek) and senescence inhibition by co-treatment with silver nanoparticles

Authors
Karuppanapandian, ThirupathiWang, Hong WeiPrabakaran, NatarajanJeyalakshmi, KandhaveluKwon, MiManoharan, KumariahKim, Wook
Issue Date
Feb-2011
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Keywords
2,4-Dichlorophenoxyacetic acid; Ethylene; Leaf senescence; Mung bean; Nuclear DNA fragmentation; Silver nanoparticles
Citation
PLANT PHYSIOLOGY AND BIOCHEMISTRY, v.49, no.2, pp.168 - 177
Indexed
SCIE
SCOPUS
Journal Title
PLANT PHYSIOLOGY AND BIOCHEMISTRY
Volume
49
Number
2
Start Page
168
End Page
177
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/113166
DOI
10.1016/j.plaphy.2010.11.007
ISSN
0981-9428
Abstract
Leaf senescence induced by 2,4-dichlorophenoxyacetic acid (2,4-D) and senescence inhibition caused by supplementation with silver (Ag+) ions in the form of silver nitrate (AgNO3) or silver nanoparticles (AgNPs) were investigated in 8-day-old mung bean (Vigna radiata L. Wilczek) seedlings. Inhibition of root and shoot elongation were observed in mung bean seedlings treated with 500 mu M 2,4-D. Concomitantly, the activity of 1-aminocyclopropane-1-carboxylic acid synthase was significantly induced in leaf tissue. Leaf senescence induced by 2,4-D was closely associated with lipid peroxidation as well as increased levels of cytotoxic hydrogen peroxide (H2O2) and superoxide radicals (O-2(center dot-)). Despite decreased catalase activity, the activities of peroxidase, superoxide dismutase, monodehydroascorbate reductase, dehydroascorbate reductase, and glutathione reductase were increased during 2,4-D-induced leaf senescence. Further, the levels of reduced ascorbate, oxidized ascorbate, and reduced glutathione were markedly decreased, whereas the level of oxidized glutathione increased. 2,4-D-induced leaf senescence in mung bean was accompanied by an increase in positive terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling, nuclear DNA fragmentation, and the activity of a 15-kDa Ca2+-dependent DNase. Supplementation with 100 mu M AgNO3 or AgNPs inhibited 2,4-D-induced leaf senescence. The present results suggest that increased oxidative stress (O-2(center dot-) and H2O2) led to senescence in mung bean leaves. Furthermore, significantly induced antioxidative enzymes are not sufficient to protect mung bean cells from 2,4-D-induced harmful ROS. (C) 2010 Elsevier Masson SAS. All rights reserved.
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