首页> 美国卫生研究院文献>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
【2h】

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Alamethicin是挥发性强的引发剂 生物合成和卷须卷材。茉莉和柠檬之间的相声 利马豆中的水杨酸信号

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 A2 do not prevent the coiling reaction.
机译:Alamethicin(ALA)是来自木霉属木霉的电压门控,形成离子通道的肽混合物,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,所发射物质的混合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生茉莉酸的质谱分析表明,ALA主要通过十八烷类信号通路(茉莉酸增加了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,并且内源性水杨酸酯的生产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-氧代苯乙二酸下游生物合成途径中的步骤,从而将释放出的挥发物减少为先前显示的化合物 由早期的十八烷诱导。 ALA也会引起卷须卷曲 在各种物种中,例如Pisum,Lathyrus, 和Bryonia,但回应似乎是独立的 来自十八烷类生物合成,因为脂氧合酶和 磷脂酶A2不会阻止卷曲 反应。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号