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Arabidopsis Responds to Alternaria alternata Volatiles by Triggering Plastid Phosphoglucose Isomerase-Independent Mechanisms

机译:拟南芥通过触发质体磷酸葡萄糖异构酶非依赖性机制来响应链格孢。

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摘要

Volatile compounds (s) emitted by phylogenetically diverse microorganisms (including plant pathogens and microbes that do not normally interact mutualistically with plants) promote photosynthesis, growth, and the accumulation of high levels of starch in leaves through cytokinin ()-regulated processes. In Arabidopsis (Arabidopsis thaliana) plants not exposed to s, plastidic phosphoglucose isomerase (pPGI) acts as an important determinant of photosynthesis and growth, likely as a consequence of its involvement in the synthesis of plastidic s in roots. Moreover, this enzyme plays an important role in connecting the Calvin-Benson cycle with the starch biosynthetic pathway in leaves. To elucidate the mechanisms involved in the responses of plants to microbial s and to investigate the extent of pPGI involvement, we characterized pPGI-null pgi1-2 Arabidopsis plants cultured in the presence or absence of s emitted by Alternaria alternata. We found that volatile emissions from this fungal phytopathogen promote growth, photosynthesis, and the accumulation of plastidic s in pgi1-2 leaves. Notably, the mesophyll cells of pgi1-2 leaves accumulated exceptionally high levels of starch following exposure. Proteomic analyses revealed that s promote global changes in the expression of proteins involved in photosynthesis, starch metabolism, and growth that can account for the observed responses in pgi1-2 plants. The overall data show that Arabidopsis plants can respond to s emitted by phytopathogenic microorganisms by triggering pPGI-independent mechanisms.
机译:系统发育上多种多样的微生物(包括通常与植物不相互作用的植物病原体和微生物)释放的挥发性化合物可通过细胞分裂素调节过程,促进光合作用,生长以及高水平淀粉在叶片中的积累。在未暴露于s的拟南芥(Arabidopsis thaliana)植物中,质体磷酸葡萄糖异构酶(pPGI)是光合作用和生长的重要决定因素,可能是由于其参与了根系质体s的合成。此外,该酶在将Calvin-Benson循环与叶片中的淀粉生物合成途径相联系方面起着重要作用。为了阐明涉及植物对微生物的反应的机制并调查pPGI参与的程度,我们对在存在或不存在链格孢菌的情况下培养的pPGI空pgi1-2拟南芥植株进行了表征。我们发现,这种真菌性植物病原体的挥发性排放物促进pgi1-2叶片中的生长,光合作用和质体的积累。值得注意的是,暴露后pgi1-2叶的叶肉细胞积累了异常高水平的淀粉。蛋白质组学分析显示s可促进参与光合作用,淀粉代谢和生长的蛋白质表达的整体变化,这可解释在pgi1-2植物中观察到的反应。总体数据表明,拟南芥植物可以通过触发pPGI独立机制来响应植物致病性微生物释放的s。

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