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亚麻感染镰刀菌后果胶代谢的变化。

The changes in pectin metabolism in flax infected with Fusarium.

机构信息

Faculty of Biotechnology, University of Wroclaw, Przybyszewskiego 63/77, 51-148 Wroclaw, Poland.

出版信息

Plant Physiol Biochem. 2011 Aug;49(8):862-72. doi: 10.1016/j.plaphy.2011.03.002. Epub 2011 Mar 23.

Abstract

Fusarium culmorum and Fusarium oxysporum are the most common fungal pathogens of flax (Linum usitatissimum L.), thus leading to the greatest losses in crop yield. A subtractive cDNA library was constructed from flax seedlings exposed for two days to F. oxysporum. This revealed a set of genes that are potentially involved in the flax defense responses. Two of those genes directly participate in cell wall sugar polymer metabolism: UDP-D-glucuronate 4-epimerase (GAE; EC 5.1.3.6) and formate dehydrogenase (FDH; EC 1.2.1.2). GAE delivers the main substrate for pectin biosynthesis, and decreases were detected in its mRNA level after Fusarium infection. FDH participates in the metabolism of formic acid, and the expression level of its gene increased after Fusarium infection. However, metabolite profiling analysis disclosed that the pectin content in the infected plants remained unchanged, but that there were reductions in both the levels of the soluble sugars that serve as pectin precursors, and in the level of formic acid. Since formic acid is the product of pectin demethylesterification, the level of mRNAs coding for pectin methylesterase (EC 3.1.1.11) in the infected flax was measured, revealing a decrease in its expression upon plant infection. Transgenic flax plants overexpressing fungal polygalacturonase (EC 3.2.1.15) and rhamnogalacturonase (EC 3.2.1.-) showed a decrease in the pectin content and an elevated level of formic acid, but the level of expression of the FDH gene remained unchanged. It is suspected that the expression of the formate dehydrogenase gene is directly controlled by the pathogen in the early stage of infection, and additionally by pectin degradation in the later stages.

摘要

尖孢镰刀菌和腐皮镰刀菌是亚麻(Linum usitatissimum L.)最常见的真菌病原体,因此导致作物产量损失最大。从暴露于腐皮镰刀菌两天的亚麻幼苗中构建了一个消减 cDNA 文库。这揭示了一组可能参与亚麻防御反应的基因。其中两个基因直接参与细胞壁糖聚合物代谢:UDP-D-葡萄糖醛酸 4-差向异构酶(GAE;EC 5.1.3.6)和甲酸盐脱氢酶(FDH;EC 1.2.1.2)。GAE 提供果胶生物合成的主要底物,在腐皮镰刀菌感染后其 mRNA 水平下降。FDH 参与甲酸代谢,其基因表达水平在腐皮镰刀菌感染后增加。然而,代谢物分析显示感染植物中的果胶含量保持不变,但作为果胶前体的可溶性糖水平和甲酸水平降低。由于甲酸是果胶脱甲基化的产物,因此测量了感染亚麻中编码果胶甲酯酶(EC 3.1.1.11)的 mRNA 水平,发现植物感染后其表达下降。过表达真菌聚半乳糖醛酸酶(EC 3.2.1.15)和鼠李半乳糖醛酸酶(EC 3.2.1.-)的转基因亚麻植物表现出果胶含量降低和甲酸水平升高,但 FDH 基因的表达水平保持不变。怀疑甲酸脱氢酶基因的表达在感染早期直接受到病原体的控制,在后期还受到果胶降解的影响。

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