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氧脂类亲电试剂与谷胱甘肽的加合物反映了烟草过敏反应中下游脂氧合酶途径的一种特异性。

Adducts of oxylipin electrophiles to glutathione reflect a 13 specificity of the downstream lipoxygenase pathway in the tobacco hypersensitive response.

作者信息

Davoine Céline, Falletti Olivier, Douki Thierry, Iacazio Gilles, Ennar Najla, Montillet Jean-Luc, Triantaphylidès Christian

机构信息

Laboratoire de Radiobiologie Végétale, DSV-Département d'Ecophysiologie Végétale et de Microbiologie, CEA-Cadarache, 13108 Saint-Paul Lez Durance cedex, France.

出版信息

Plant Physiol. 2006 Apr;140(4):1484-93. doi: 10.1104/pp.105.074690. Epub 2006 Feb 24.

Abstract

The response to reactive electrophile species (RES) is now considered as part of the plant response to pathogen and insect attacks. Thanks to a previously established high-performance liquid chromatography tandem mass spectrometry methodology, we have investigated the production of oxylipin RES adducts to glutathione (GSH) during the hypersensitive response (HR) of plants. We have observed that RES conjugation to GSH in tobacco (Nicotiana tabacum) leaves is facile and nonspecific. In cryptogein-elicited tobacco leaves, we show that the oxylipin RES adducts to GSH are produced in correlation with GSH consumption, increase in glutathione S-transferase activity, and the appearance of the cell death symptoms. In this model, the adducts arise mainly from the downstream 13 lipoxygenase (LOX) metabolism, although the induced 9 LOX pathway leads massively to the accumulation of upstream metabolites. The main adducts were obtained from 2-hexenal and 12-oxo-phytodienoic acid. They accumulate transiently as 1-hexanol-3-GSH, a reduced adduct, and 12-oxo-phytodienoic acid-GSH, respectively. RES conjugation does not initiate cell death but explains part of the GSH depletion that accompanies HR cell death. The nature of these GSH conjugates shows the key role played by the 13 LOX pathway in RES signaling in the tobacco HR.

摘要

对活性亲电物质(RES)的反应现在被认为是植物对病原体和昆虫攻击反应的一部分。借助先前建立的高效液相色谱串联质谱方法,我们研究了植物过敏反应(HR)期间氧脂RES与谷胱甘肽(GSH)加合物的产生。我们观察到,烟草(Nicotiana tabacum)叶片中RES与GSH的结合很容易且是非特异性的。在隐地蛋白诱导的烟草叶片中,我们表明氧脂RES与GSH的加合物是与GSH消耗、谷胱甘肽S-转移酶活性增加以及细胞死亡症状的出现相关产生的。在这个模型中,加合物主要来自下游的13-脂氧合酶(LOX)代谢,尽管诱导的9-LOX途径大量导致上游代谢物的积累。主要的加合物分别来自2-己烯醛和12-氧代-植物二烯酸。它们分别以还原加合物1-己醇-3-GSH和12-氧代-植物二烯酸-GSH的形式短暂积累。RES结合不会引发细胞死亡,但解释了伴随HR细胞死亡的部分GSH消耗。这些GSH共轭物的性质表明13-LOX途径在烟草HR的RES信号传导中起关键作用。

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