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首页> 外文期刊>Plant physiology >Ion channel-forming alamethicin is a potent elicitor of volatile biosynthesis and tendril coiling. Cross talk between jasmonate and salicylate signaling in lima bean
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Ion channel-forming alamethicin is a potent elicitor of volatile biosynthesis and tendril coiling. Cross talk between jasmonate and salicylate signaling in lima bean

机译:形成离子通道的阿拉美霉素是挥发性生物合成和卷须卷曲的有效引发剂。利马豆中茉莉酸和水杨酸信号之间的串扰

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摘要

Alamethicin (ALA), a voltage-gated, ion channel-forming peptide mixture from Trichoderma viride, is a potent elicitor of the biosynthesis of volatile compounds in lima bean (Phaseolus lunatus). Unlike elicitation with jasmonic acid or herbivore damage, the blend of substances emitted comprises only the two homoterpenes, 4,11-dimethylnona-1,3,7-triene and 4,8,12-trimethyltrideca-1,3,7,11-tetraene and methyl salicylate. Inhibition of octadecanoid signaling by aristolochic acid and phenidone as well as mass spectrometric analysis of endogenous jasmonate demonstrate that ALA induces the biosynthesis of volatile compounds principally via the octadecanoid-signaling pathway (20-fold increase of jasmonic acid). ALA also up-regulates salicylate biosynthesis, and the time course of the production of endogenous salicylate correlates well with the appearance of the methyl ester in the gas phase. The massive up-regulation of the SA-pathway (90-fold) interferes with steps in the biosynthetic pathway downstream of 12-oxophytodienoic acid and thereby reduces the pattern of emitted volatiles to compounds previously shown to be induced by early octadecanoids. ALA also induces tendril coiling in various species like Pisum, Lathyrus, and Bryonia, but the response appears to be independent from octadecanoid biosynthesis, because inhibitors of lipoxygenase and phospholipase A(2) do not prevent the coiling reaction. [References: 56]
机译:Alamethicin(ALA)是一种来自木霉属木霉的电压门控型离子通道形成肽混合物,是利马豆(Phaseolus lunatus)中挥发性化合物生物合成的有效引发剂。与茉莉酸或草食动物的危害不同,所散发的物质共混物仅包含两个高萜类化合物,即4,11-二甲基壬基-1,3,7-三烯和4,8,12-三甲基三苯胺-1,3,7,11-丁烯和水杨酸甲酯。马兜铃酸和菲尼酮对十八烷类信号的抑制作用以及内源性茉莉酮酸酯的质谱分析表明,ALA主要通过十八烷类信号通路(茉莉酸的含量增加了20倍)诱导了挥发性化合物的生物合成。 ALA还上调了水杨酸酯的生物合成,内源性水杨酸酯生产的时间过程与气相中甲酯的出现密切相关。 SA途径的大量上调(90倍)干扰了12-氧代苯乙二酸下游的生物合成途径中的步骤,从而将释放的挥发物的模式降低为先前显示为早期十八烷类化合物诱导的化合物。 ALA还会在各种物种(如Pisum,Lathyrus和Bryonia)中诱发卷须卷曲,但响应似乎与十八烷类生物合成无关,因为脂氧合酶和磷脂酶A(2)的抑制剂不会阻止卷曲反应。 [参考:56]

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