Characterization of reactive oxygen species-involved oxidative damage in Hapalosiphon species crude extract-treated wheat [Triticum aestivum] and onion [Allium cepa] roots

Crude extract-induced oxidative damage using the cyanobacterium, Hapalosiphon sp., was investigated in wheat seedlings (Triticum aestivum L. cv. Norin 61) and onion seedlings (Allium cepa L. cv. Raputa II).The analysis of root cell viability or cell death using Evans blue uptake showed that the root...

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Published inWeed biology and management Vol. 7; no. 3; pp. 172 - 177
Main Authors Sanevas, N.(Tsukuba Univ., Ibaraki (Japan)), Sunohara, Y, Matsumoto, H
Format Journal Article
LanguageEnglish
Published Melbourne, Australia Blackwell Publishing Asia 01.09.2007
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Summary:Crude extract-induced oxidative damage using the cyanobacterium, Hapalosiphon sp., was investigated in wheat seedlings (Triticum aestivum L. cv. Norin 61) and onion seedlings (Allium cepa L. cv. Raputa II).The analysis of root cell viability or cell death using Evans blue uptake showed that the root-tip cells of wheat and onion lost viability after 24 h and 48 h treatment with 3 g dry weight (DW)/L of the crude extract, respectively. Lipid peroxidation was induced in the roots of both species and the shoots of onion, whereas no increase in lipid peroxide formation was observed in the wheat shoots. In onion, the degree of random DNA fragmentation increased with the increasing concentration of the extract and laddering of the DNA was observed with 6 g DW/L of the extract, but no apparent DNA ladder formation occurred in the wheat. Pretreatment for 1 h with the NADPH oxidase inhibitors, diphenyle-neidonium or imidazole, reduced the crude extract-induced root cell death in both species. From the results, we suggest that the Hapalosiphon sp. crude extract might enhance reactive oxygen species (ROS) production, which causes membrane lipid damage and fragmentation of the DNA of plant cells, resulting in cell death and growth inhibition. The crude extract-mediated phytotoxic damage might be caused by ROS, triggered by NADPH oxidase.
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http://dx.doi.org/10.1111/j.1445-6664.2007.00253.x
istex:119D76D4B06F4B5DE9C0CEC477F665CBC3B114C4
ark:/67375/WNG-H36TKBV1-S
ArticleID:WBM253
ISSN:1444-6162
1445-6664
DOI:10.1111/j.1445-6664.2007.00253.x