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叶片提取的、依赖 NARK 和结瘤因子的低分子质量分数抑制大豆过度分枝。

Suppression of hypernodulation in soybean by a leaf-extracted, NARK- and Nod factor-dependent, low molecular mass fraction.

机构信息

Australian Research Council Centre of Excellence for Integrative Legume Research, The University of Queensland, St Lucia, QLD, Australia.

出版信息

New Phytol. 2010 Mar;185(4):1074-86. doi: 10.1111/j.1469-8137.2009.03163.x. Epub 2010 Jan 20.

Abstract

*Legumes regulate the number of nodules they form via a process called autoregulation of nodulation (AON). This involves a shoot-derived inhibitor (SDI) molecule that is synthesized in the shoots and is transported down to the roots where it inhibits further nodule development. *To characterize SDI, we developed a novel feeding bioassay. This involved feeding aqueous leaf extracts directly into the petiole of hypernodulating and supernodulating nark mutant plants of Glycine max (soybean). These mutants normally exhibit an increased nodulation phenotype because SDI is not produced and thus AON is nonfunctional. *Feeding wild-type leaf extracts presumed to contain SDI was successful in suppressing the increased nodulation phenotype, whereas feeding with Gmnark leaf extracts did not. Suppression activity was inoculation-dependent, Nod factor-dependent, required GmNARK activity, and was heat-, Proteinase K- and ribonuclease A-resistant. Wild-type extracts maintained suppressive activity even at a ninefold dilution. Sinorhizobium meliloti-inoculated Medicago truncatula leaf extracts from wild-type, but not from supernodulating mutant Mtsunn, suppressed hypernodulation in soybean. *Our results demonstrate that the petiole feeding bioassay is an efficient and effective technique to introduce aqueous extracts into plants. They also demonstrate that SDI is a small compound with an apparent molecular mass of < 1000 Da and is unlikely to be a protein or an RNA molecule.

摘要

豆科植物通过一种称为结瘤自动调控(AON)的过程来调节其形成的根瘤数量。这个过程涉及到一种由芽合成并向下运输到根部的芽抑制物(SDI)分子,它可以抑制根瘤的进一步发育。为了研究 SDI,我们开发了一种新的饲喂生物测定法。该方法涉及直接将水提叶片提取物饲喂到大豆超结瘤突变体 nark 的叶柄中。这些突变体通常表现出增加的结瘤表型,因为没有合成 SDI,所以 AON 失去了功能。饲喂被认为含有 SDI 的野生型叶片提取物成功地抑制了增加的结瘤表型,而饲喂 Gmnark 叶片提取物则没有。抑制活性依赖于接种、结瘤因子、GmNARK 活性,并且对热、蛋白酶 K 和核糖核酸酶 A 具有抗性。野生型提取物即使在九倍稀释后仍保持抑制活性。来自野生型但不是超结瘤突变体 Mtsunn 的接种了根瘤菌的紫花苜蓿叶片提取物抑制了大豆的过度结瘤。我们的结果表明,叶柄饲喂生物测定法是一种将水提物引入植物的有效技术。它们还表明,SDI 是一种小化合物,其表观分子量<1000Da,不太可能是蛋白质或 RNA 分子。

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