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Nod Factor and Elicitors Activate Different Phospholipid Signaling Pathways in Suspension-Cultured Alfalfa Cells1

机译:悬浮培养苜蓿细胞中的Nod因子和激发子激活了不同的磷脂信号通路

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摘要

Lipo-chitooligosaccharides (Nod factors) are produced by symbiotic Rhizobium sp. bacteria to elicit Nod responses on their legume hosts. One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to trigger the formation of PA in nonlegume plants. To investigate how host plants can distinguish between symbionts and pathogens, the effects of Nod factor and elicitors (chitotetraose and xylanase) on the formation of PA were investigated in suspension-cultured alfalfa (Medicago sativa) cells. Theoretically, PA can be synthesized via two signaling pathways, i.e. via phospholipase D (PLD) and via phospholipase C in combination with diacylglycerol (DAG) kinase. Therefore, a strategy involving differential radiolabeling with [32P]orthophosphate was used to determine the contribution of each pathway to PA formation. In support, PLD activity was specifically measured by using the ability of the enzyme to transfer the phosphatidyl group of its substrate to a primary alcohol. In practice, Nod factor, chitotetraose, and xylanase induced the formation of PA and its phosphorylated product DAG pyrophosphate within 2 min of treatment. However, whereas phospholipase C and DAG kinase were activated during treatment with all three different compounds, PLD was only activated by Nod factor. No evidence was obtained for the activation of phospholipase A2.
机译:脂壳寡糖(Nod因子)是由共生根瘤菌(Rhizobium sp。)产生的。细菌在豆类宿主上引发Nod反应。最早的反应之一是磷脂酸(PA)的形成,磷脂酸是植物细胞中一种新型的第二信使。值得注意的是,也有病原体触发了非豆科植物中PA的形成。为了研究寄主植物如何区分共生菌和病原体,在悬浮培养的苜蓿(苜蓿)细胞中研究了Nod因子和引发剂(壳四糖和木聚糖酶)对PA形成的影响。从理论上讲,PA可以通过两种信号途径合成,即通过磷脂酶D(PLD)和通过磷脂酶C与二酰基甘油(DAG)激酶结合而合成。因此,使用涉及用[32P]正磷酸盐进行差异放射性标记的策略来确定每种途径对PA形成的贡献。在支持物上,通过使用酶将其底物的磷脂酰基团转移至伯醇的能力来具体测量PLD活性。在实践中,Nod因子,壳四糖和木聚糖酶可在处理后2分钟内诱导PA及其磷酸化产物DAG焦磷酸盐的形成。但是,虽然磷脂酶C和DAG激酶在用所有三种不同化合物治疗期间均被激活,但PLD仅被Nod因子激活。没有证据表明激活了磷脂酶A2。

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